Luminescent tungsten() complexes as photocatalysts for light-driven C-C and C-B bond formation reactions

The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten( vi ) complex which can be conveniently prepared at the gram-s...

Full description

Saved in:
Bibliographic Details
Published inChemical science (Cambridge) Vol. 11; no. 25; pp. 637 - 6382
Main Authors Yu, Daohong, To, Wai-Pong, Tong, Glenna So Ming, Wu, Liang-Liang, Chan, Kaai-Tung, Du, Lili, Phillips, David Lee, Liu, Yungen, Che, Chi-Ming
Format Journal Article
LanguageEnglish
Published CAMBRIDGE Royal Soc Chemistry 07.07.2020
Royal Society of Chemistry
Subjects
Aromatic compounds
Bonding
Bromides
Carboxylic acids
Chemistry
Chemistry, Multidisciplinary
Coupling
Covalent bonds
Electromagnetic absorption
Esters
Functional groups
Halides
NMR
Nuclear magnetic resonance
Photocatalysis
Photocatalysts
Photochemical reactions
Photoluminescence
Physical Sciences
Science & Technology
Tungsten
CROSS-COUPLING REACTIONS
ELECTRON-TRANSFER
ARYL HALIDES
IRON COMPLEXES
TRANSFER RADICAL-ADDITION
EMISSION QUANTUM YIELDS
DECARBOXYLATIVE ALKYLATION
LIVED EXCITED-STATES
METAL-FREE
PHOTOREDOX CATALYSIS
Online AccessGet full text

Cover

Abstract The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten( vi ) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance. A luminescent tungsten( vi ) complex catalyses a broad spectrum of light-driven organic transformation reactions with high product yields and good functional group tolerance.
AbstractList The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten(vi) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten(vi) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.
The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten( vi ) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance. A luminescent tungsten( vi ) complex catalyses a broad spectrum of light-driven organic transformation reactions with high product yields and good functional group tolerance.
A luminescent tungsten( vi ) complex catalyses a broad spectrum of light-driven organic transformation reactions with high product yields and good functional group tolerance. The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten( vi ) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C–C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.
The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten(VI) complex which can be conveniently prepared at the gramscale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.
The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten(vi) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C-C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.
The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large scale. Herein an air-stable, visible-light-absorbing photoluminescent tungsten( vi ) complex which can be conveniently prepared at the gram-scale is described. This complex could catalyse photochemical organic transformation reactions including borylation of aryl halides, such as aryl chloride, reductive coupling of benzyl bromides for C–C bond formation, reductive coupling of phenacyl bromides, and decarboxylative coupling of redox-active esters of alkyl carboxylic acid with high product yields and broad functional group tolerance.
Author Che, Chi-Ming
Liu, Yungen
Yu, Daohong
To, Wai-Pong
Du, Lili
Chan, Kaai-Tung
Phillips, David Lee
Wu, Liang-Liang
Tong, Glenna So Ming
AuthorAffiliation Department of Chemistry
Southern University of Science and Technology
The University of Hong Kong
State Key Laboratory of Synthetic Chemistry
HKU-CAS Joint Laboratory on New Materials
HKU Shenzhen Institute of Research and Innovation Shenzhen
AuthorAffiliation_xml – name: State Key Laboratory of Synthetic Chemistry
– name: Southern University of Science and Technology
– name: Department of Chemistry
– name: HKU Shenzhen Institute of Research and Innovation Shenzhen
– name: The University of Hong Kong
– name: HKU-CAS Joint Laboratory on New Materials
– name: a Department of Chemistry , Southern University of Science and Technology , Shenzhen , Guangdong 518055 , China . Email: cmche@hku.hk
– name: c HKU Shenzhen Institute of Research and Innovation Shenzhen , Guangdong 518055 , China
– name: b State Key Laboratory of Synthetic Chemistry , HKU-CAS Joint Laboratory on New Materials , Department of Chemistry , The University of Hong Kong , Pokfulam Road , Hong Kong , China
Author_xml – sequence: 1
  givenname: Daohong
  surname: Yu
  fullname: Yu, Daohong
– sequence: 2
  givenname: Wai-Pong
  surname: To
  fullname: To, Wai-Pong
– sequence: 3
  givenname: Glenna So Ming
  surname: Tong
  fullname: Tong, Glenna So Ming
– sequence: 4
  givenname: Liang-Liang
  surname: Wu
  fullname: Wu, Liang-Liang
– sequence: 5
  givenname: Kaai-Tung
  surname: Chan
  fullname: Chan, Kaai-Tung
– sequence: 6
  givenname: Lili
  surname: Du
  fullname: Du, Lili
– sequence: 7
  givenname: David Lee
  surname: Phillips
  fullname: Phillips, David Lee
– sequence: 8
  givenname: Yungen
  surname: Liu
  fullname: Liu, Yungen
– sequence: 9
  givenname: Chi-Ming
  surname: Che
  fullname: Che, Chi-Ming
BackLink https://www.ncbi.nlm.nih.gov/pubmed/32874518$$D View this record in MEDLINE/PubMed
BookMark eNqNkstv1DAQhy1URMvSC3dQEJcCCthx4rUvSJDyklbiAJwtx3Z2XSX21nb6-O-Z7W4XqBDClxlpvvH85vEQHfjgLUKPCX5NMBVvDE4aE1pjcw8dVbgmJWuoONj7FT5ExymdYXiUkqaaP0CHtOLzuiH8CK0W0-i8Tdr6XOTJL1O2_uRFocO4HuyVTYVKxXoVctAqq-E65VT0IRaDW65yaaK7sL5oy7ZQ3oB9X3QBHCBGlV3wRbRKb5z0CN3v1ZDs8c7O0I-PH763n8vF109f2neLUoPUXIqec8aUYZybSvUglGIhKDeiI6KnjBnLTMcb3jRdjzusOae9tZ1qLBHMVHSG3m7_XU_daM2mr6gGuY5uVPFaBuXknxHvVnIZLuS8rnkD5WboZPdBDOeTTVmODsYzDMrbMCVZ1VQwmOScAfr8DnoWpuihPaCIwIQJJoB6-ruivZTbJQDwagtc2i70STvrtd1jsLemBm21AK-iQPP_p1uXb_bQhslnSMXbVB1DStH2Uu_iMAk3SILl5qbkKf7W3tzUKaS8vJNyW-mv8JMtHJPec78OFOLP_hWXa9PTn4N53xM
CitedBy_id crossref_primary_10_1002_advs_202404866
crossref_primary_10_1039_D3GC04635D
crossref_primary_10_1039_D4GC04495A
crossref_primary_10_1039_D4SC02784A
crossref_primary_10_1002_adsc_202301498
crossref_primary_10_1039_D1OB00323B
crossref_primary_10_6023_cjoc202110019
crossref_primary_10_1002_cctc_202201288
crossref_primary_10_1021_acs_chemrev_0c01236
crossref_primary_10_1021_jacs_1c07617
crossref_primary_10_1021_acs_joc_3c02986
crossref_primary_10_1021_acs_inorgchem_1c03767
crossref_primary_10_1002_ange_202213207
crossref_primary_10_1021_acs_organomet_0c00733
crossref_primary_10_1039_D1SC04258K
crossref_primary_10_1021_acs_joc_3c00141
crossref_primary_10_1016_j_jphotochemrev_2023_100589
crossref_primary_10_1055_a_1390_9065
crossref_primary_10_1039_D4CC00169A
crossref_primary_10_1021_acs_inorgchem_3c03557
crossref_primary_10_1063_5_0086718
crossref_primary_10_1021_acs_orglett_2c01699
crossref_primary_10_1038_s41557_024_01446_8
crossref_primary_10_1039_D2QO01140A
crossref_primary_10_1002_asia_202100784
crossref_primary_10_1016_j_saa_2022_120881
crossref_primary_10_1039_D3CY00443K
crossref_primary_10_1021_acs_joc_4c02831
crossref_primary_10_1039_D4OB01913J
crossref_primary_10_1039_D2QO00401A
crossref_primary_10_1002_slct_202204417
crossref_primary_10_1021_acs_accounts_3c00184
crossref_primary_10_1007_s11426_024_2345_0
crossref_primary_10_1039_D3CS00871A
crossref_primary_10_1021_acs_joc_3c02552
crossref_primary_10_6023_cjoc202212041
crossref_primary_10_1002_anie_202213207
crossref_primary_10_34133_icomputing_0037
Cites_doi 10.1126/science.aat9750
10.1002/pola.27435
10.1002/anie.201408940
10.1002/anie.201002285
10.1039/C6CC09725A
10.1016/S0010-8545(02)00034-6
10.1021/jacs.9b07370
10.1002/ejoc.201900952
10.1016/j.ccr.2019.213129
10.1021/jo991478s
10.1038/s41586-018-0366-x
10.1002/cctc.201600320
10.1002/anie.201906381
10.1016/S0020-1693(96)05432-1
10.1093/nsr/nwx039
10.1021/jacs.9b00917
10.1016/j.trechm.2019.01.008
10.1039/C5CC06917C
10.1002/anie.201910348
10.1039/C6QO00109B
10.1021/acs.joc.6b01034
10.1002/anie.201915762
10.1016/S0020-1693(00)91697-9
10.1039/C39870000546
10.1002/anie.201606323
10.1002/chem.201703602
10.1016/j.ccr.2018.01.003
10.1021/acscatal.9b01394
10.1002/chem.201603517
10.1039/C9SC04288A
10.1002/anie.201814488
10.1021/acs.joc.6b01449
10.1002/chem.200305285
10.1021/j100365a039
10.1002/anie.201107028
10.1126/science.1258232
10.1021/ol202740w
10.1055/s-1995-4883
10.1021/jacs.8b03744
10.1016/S0020-1693(96)05335-2
10.1039/C6CC05867A
10.1038/nature17438
10.1021/acscatal.5b01071
10.1038/s41570-017-0052
10.1021/ja00024a074
10.1016/j.tetlet.2010.12.007
10.1002/anie.201501556
10.1002/adsc.201701615
10.1021/jacs.8b08720
10.1039/C9SC02000D
10.1039/C8SC01219A
10.1021/jacs.6b01376
10.1002/chem.201405356
10.1039/C8CY02336K
10.1021/jacs.6b02723
10.1039/C5SC02185E
10.1021/jacs.8b08781
10.1002/anie.201400420
10.1039/C4SC01105H
10.1016/j.jcat.2007.11.008
10.1039/C5CS00338E
10.1021/acscatal.9b04411
10.1039/C7CS00226B
10.1021/acscatal.9b02220
10.1002/anie.201501220
10.1021/ja300798k
10.1039/C8CC06375C
10.1002/adsc.201701389
10.1039/C6SC04607J
10.1002/anie.201707537
10.1002/ejoc.201701461
10.1002/anie.201906698
10.1016/j.catcom.2017.12.012
10.1002/adsc.201500734
10.1039/p29840001705
10.1021/acs.orglett.7b01518
10.1002/anie.201609035
10.1021/acs.orglett.5b00282
10.1039/C7SC05320G
10.1021/jacs.6b05712
10.1039/C7DT02632C
10.1021/jacs.9b12328
10.1039/C4SC01072H
10.1016/S0025-5408(99)00148-8
10.1021/jacs.6b05436
10.1002/anie.201804873
10.1021/acs.orglett.5b02532
10.1002/anie.201806966
10.1016/S1387-7003(00)00034-4
10.1021/ja108560e
10.1021/cr00039a007
10.1021/jacs.9b07373
10.1021/jacs.6b02248
10.1039/C7SC02479G
10.1021/jacs.7b09802
10.1039/c39890001636
10.1039/c39830000513
10.1126/science.aau7160
10.1039/DT9920003325
10.1002/anie.201804022
10.1002/anie.201800818
10.1021/jacs.7b13281
10.1039/C7DT00400A
10.1039/C6NJ03265F
10.1002/anie.201608240
10.1002/ejic.201700064
10.1039/C6GC01101B
10.1002/asia.201601712
10.1021/jacs.6b11813
10.1021/ja00443a083
10.1002/anie.201201666
10.1002/anie.201306727
10.1021/ja510973h
10.1246/cl.1993.2021
10.1021/ol501619w
10.1002/anie.201808642
10.1039/C9SC04584H
10.1021/jacs.7b13131
10.1021/acscatal.8b03498
10.1002/anie.201605571
10.1021/acs.orglett.6b02553
10.1002/anie.201707193
10.1021/jacs.5b05411
10.1002/chem.201901618
10.1039/C6SC03303B
10.1021/jacs.7b03538
10.1021/acs.orglett.7b03587
10.1021/jacs.9b10678
10.1021/acs.orglett.9b01450
10.1021/ja500031m
10.1021/ja012247h
10.1002/anie.201203599
10.1002/anie.201301149
10.1002/ijch.201600115
10.1002/chem.201806345
10.1039/C6SC03775E
10.1021/ja00234a047
10.1021/ja808658b
10.1039/C5SC04521E
10.1002/cptc.201700077
10.1021/acs.accounts.6b00284
10.1039/C8CC04048F
10.1021/acscatal.8b01863
10.1021/jacs.6b05934
10.1002/chem.201700103
10.1002/anie.201102306
10.1002/anie.201101379
10.1021/ic00122a021
10.1039/C9CS00573K
10.1021/jacs.8b00742
10.1021/acscatal.5b01573
10.1038/ncomms10093
10.1002/anie.201709766
10.1038/nature21430
10.1039/c7sc02479g
10.1039/c4sc01105h
10.1039/c7cs00226b
10.1039/c6sc03775e
10.1039/c5cs00338e
10.1039/c5cc06917c
10.1039/c6cc05867a
10.1039/c5sc04521e
10.1039/c7sc05320g
10.1039/c4sc01072h
10.1039/c7dt00400a
10.1039/c6sc03303b
10.1039/c6sc04607j
10.1039/c8sc01219a
10.1039/c8cc06375c
10.1039/c6nj03265f
10.1039/c9cs00573k
10.1039/c6qo00109b
10.1039/c6cc09725a
10.1039/c6gc01101b
10.1039/c5sc02185e
10.1039/c8cc04048f
10.1039/c9sc04584h
10.1039/c8cy02336k
10.1039/c7dt02632c
10.1039/c9sc02000d
10.1039/c9sc04288a
ContentType Journal Article
Copyright This journal is © The Royal Society of Chemistry 2020.
Copyright Royal Society of Chemistry 2020
This journal is © The Royal Society of Chemistry 2020 2020
Copyright_xml – notice: This journal is © The Royal Society of Chemistry 2020.
– notice: Copyright Royal Society of Chemistry 2020
– notice: This journal is © The Royal Society of Chemistry 2020 2020
DBID AAYXX
CITATION
17B
1KM
AOWDO
BLEPL
DTL
EGQ
NPM
7SR
8BQ
8FD
JG9
7X8
5PM
DOI 10.1039/d0sc01340d
DatabaseName CrossRef
Web of Knowledge
Index Chemicus
Web of Science - Science Citation Index Expanded - 2020
Web of Science Core Collection
Science Citation Index Expanded
Web of Science Primary (SCIE, SSCI & AHCI)
PubMed
Engineered Materials Abstracts
METADEX
Technology Research Database
Materials Research Database
MEDLINE - Academic
PubMed Central (Full Participant titles)
DatabaseTitle CrossRef
Web of Science
PubMed
Materials Research Database
Engineered Materials Abstracts
Technology Research Database
METADEX
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic


Web of Science
PubMed
Materials Research Database
CrossRef
Database_xml – sequence: 1
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 2
  dbid: 1KM
  name: Index Chemicus
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/woscc/search-with-editions?editions=WOS.IC
  sourceTypes:
    Enrichment Source
    Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 2041-6539
EndPage 6382
ExternalDocumentID PMC7448528
32874518
000544484900023
10_1039_D0SC01340D
d0sc01340d
Genre Journal Article
GrantInformation_xml – fundername: Shenzhen Science and Technology Innovation Committee
  grantid: JCYJ20170412140251576; JCYJ20180508162429786
– fundername: Hong Kong Research Grants Council
  grantid: HKU 17330416
– fundername: China Postdoctoral Science Foundation
  grantid: 2018M633043
– fundername: University Grants Committee Areas of Excellence Scheme
  grantid: AoE/P-03/08
– fundername: CAS-Croucher Funding Scheme for Joint Laboratories
GroupedDBID 0-7
0R
705
7~J
AAGNR
AAIWI
AAPBV
ABGFH
ACGFS
ACIWK
ADBBV
ADMRA
AENEX
AFVBQ
AGSTE
AGSWI
ALMA_UNASSIGNED_HOLDINGS
AOIJS
AUDPV
AZFZN
BCNDV
BLAPV
BSQNT
C6K
CKLOX
D0L
EE0
EF-
F5P
GROUPED_DOAJ
HYE
HZ
H~N
JG
O-G
O9-
OK1
R7C
R7D
RCNCU
ROYLF
RPM
RRC
RSCEA
RVUXY
SKA
SKF
SKH
SKJ
SKM
SKR
SKZ
SLC
SLF
SLH
SMJ
0R~
53G
AAEMU
AAFWJ
AAJAE
AARTK
AAXHV
AAYXX
ABEMK
ABIQK
ABPDG
ABXOH
AEFDR
AESAV
AFLYV
AFPKN
AGEGJ
AGRSR
AHGCF
AKBGW
ANUXI
APEMP
CITATION
H13
HZ~
PGMZT
RAOCF
RNS
17B
1KM
BLEPL
DTL
GROUPED_WOS_WEB_OF_SCIENCE
NPM
7SR
8BQ
8FD
JG9
7X8
5PM
ID FETCH-LOGICAL-c520t-9f8866ad688d2af328309938d9b19f366de6db85855bf0b0c883feeba5e196d23
ISICitedReferencesCount 42
ISICitedReferencesURI https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=CitingArticles&UT=000544484900023
ISSN 2041-6520
IngestDate Thu Aug 21 18:35:13 EDT 2025
Fri Jul 11 09:36:11 EDT 2025
Mon Jul 14 08:39:24 EDT 2025
Mon Jul 21 06:05:26 EDT 2025
Wed Aug 06 15:49:30 EDT 2025
Fri Aug 29 16:07:16 EDT 2025
Thu Apr 24 23:10:46 EDT 2025
Tue Jul 01 03:46:38 EDT 2025
Sat Jan 08 04:02:10 EST 2022
Wed Nov 11 00:26:54 EST 2020
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 25
Keywords CROSS-COUPLING REACTIONS
ELECTRON-TRANSFER
ARYL HALIDES
IRON COMPLEXES
TRANSFER RADICAL-ADDITION
EMISSION QUANTUM YIELDS
DECARBOXYLATIVE ALKYLATION
LIVED EXCITED-STATES
METAL-FREE
PHOTOREDOX CATALYSIS
Language English
License This journal is © The Royal Society of Chemistry 2020.
This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0)
LinkModel OpenURL
LogoURL https://exlibris-pub.s3.amazonaws.com/fromwos-v2.jpg
MergedId FETCHMERGED-LOGICAL-c520t-9f8866ad688d2af328309938d9b19f366de6db85855bf0b0c883feeba5e196d23
Notes 10.1039/d0sc01340d
Electronic supplementary information (ESI) available: Experimental details, photophysical data, DFT calculations and NMR spectral data. See DOI
ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
ORCID 0000-0003-3740-2305
0000-0003-4840-9051
0000-0002-2473-6173
0000-0002-6820-243X
0000-0002-5434-0786
0000-0002-2554-7219
0000-0002-9712-3925
0000-0002-8606-8780
OpenAccessLink http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000544484900023
PMID 32874518
PQID 2419016969
PQPubID 2047492
ParticipantIDs proquest_journals_2419016969
pubmed_primary_32874518
webofscience_primary_000544484900023CitationCount
crossref_primary_10_1039_D0SC01340D
rsc_primary_d0sc01340d
pubmedcentral_primary_oai_pubmedcentral_nih_gov_7448528
crossref_citationtrail_10_1039_D0SC01340D
proquest_miscellaneous_2439633176
webofscience_primary_000544484900023
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2020-07-07
PublicationDateYYYYMMDD 2020-07-07
PublicationDate_xml – month: 07
  year: 2020
  text: 2020-07-07
  day: 07
PublicationDecade 2020
PublicationPlace CAMBRIDGE
PublicationPlace_xml – name: CAMBRIDGE
– name: England
– name: Cambridge
PublicationTitle Chemical science (Cambridge)
PublicationTitleAbbrev CHEM SCI
PublicationTitleAlternate Chem Sci
PublicationYear 2020
Publisher Royal Soc Chemistry
Royal Society of Chemistry
Publisher_xml – name: Royal Soc Chemistry
– name: Royal Society of Chemistry
References Supranovich (D0SC01340D-(cit10u)/*[position()=1]) 2019; 21
Hou (D0SC01340D-(cit25c)/*[position()=1]) 2019; 10
Frem (D0SC01340D-(cit3g)/*[position()=1]) 1997; 255
Yuan (D0SC01340D-(cit9f)/*[position()=1]) 2019; 9
Zhang (D0SC01340D-(cit7e)/*[position()=1]) 2016; 8
Häring (D0SC01340D-(cit34d)/*[position()=1]) 2015; 51
Kim (D0SC01340D-(cit40e)/*[position()=1]) 2020; 142
Nguyen (D0SC01340D-(cit38a)/*[position()=1]) 2011; 133
Yin (D0SC01340D-(cit8d)/*[position()=1]) 2016; 138
Murphy (D0SC01340D-(cit10m)/*[position()=1]) 2016; 532
Yamaguchi (D0SC01340D-(cit19c)/*[position()=1]) 2012; 51
Okada (D0SC01340D-(cit29)/*[position()=1]) 1989
Liu (D0SC01340D-(cit32b)/*[position()=1]) 2017; 12
Meanwell (D0SC01340D-(cit10l)/*[position()=1]) 2016; 55
Kim (D0SC01340D-(cit34a)/*[position()=1]) 2012; 51
West (D0SC01340D-(cit9d)/*[position()=1]) 2017; 57
Shields (D0SC01340D-(cit3f)/*[position()=1]) 2018; 140
Cismesia (D0SC01340D-(cit41)/*[position()=1]) 2015; 6
Jamison (D0SC01340D-(cit26d)/*[position()=1]) 2016; 49
Chábera (D0SC01340D-(cit7a)/*[position()=1]) 2017; 543
Takematsu (D0SC01340D-(cit12d)/*[position()=1]) 2017; 46
Chen (D0SC01340D-(cit20b)/*[position()=1]) 2016; 7
Shen (D0SC01340D-(cit3e)/*[position()=1]) 2018; 9
Park (D0SC01340D-(cit24)/*[position()=1]) 2016; 22
Okada (D0SC01340D-(cit26a)/*[position()=1]) 1988; 110
Sha (D0SC01340D-(cit28)/*[position()=1]) 2018; 8
Yuan (D0SC01340D-(cit10t)/*[position()=1]) 2018; 57
Kim (D0SC01340D-(cit32e)/*[position()=1]) 2000; 65
Meanwell (D0SC01340D-(cit10r)/*[position()=1]) 2018; 54
Marzo (D0SC01340D-(cit1g)/*[position()=1]) 2018; 57
Larsen (D0SC01340D-(cit1f)/*[position()=1]) 2018; 24
Zhang (D0SC01340D-(cit7d)/*[position()=1]) 2015; 53
Chan (D0SC01340D-(cit18d)/*[position()=1]) 2017; 8
Buldt (D0SC01340D-(cit3b)/*[position()=1]) 2017; 23
Wallentin (D0SC01340D-(cit38b)/*[position()=1]) 2012; 134
Jiang (D0SC01340D-(cit30)/*[position()=1]) 2020; 11
Abrams (D0SC01340D-(cit10n)/*[position()=1]) 2017; 8
Zhu (D0SC01340D-(cit25d)/*[position()=1]) 2019; 141
Twilton (D0SC01340D-(cit1d)/*[position()=1]) 2017; 1
Büldt (D0SC01340D-(cit5a)/*[position()=1]) 2016; 55
Cui (D0SC01340D-(cit9c)/*[position()=1]) 2012
Zou (D0SC01340D-(cit45a)/*[position()=1]) 2011; 50
Malzkuhn (D0SC01340D-(cit3c)/*[position()=1]) 2018; 359
Cuttell (D0SC01340D-(cit2d)/*[position()=1]) 2002; 124
Herr (D0SC01340D-(cit5b)/*[position()=1]) 2019; 141
Zimmer (D0SC01340D-(cit7f)/*[position()=1]) 2017
Hironaka (D0SC01340D-(cit23)/*[position()=1]) 1984
Chow (D0SC01340D-(cit18c)/*[position()=1]) 2015; 54
Okada (D0SC01340D-(cit26b)/*[position()=1]) 1991; 113
Bardagi (D0SC01340D-(cit34g)/*[position()=1]) 2018
Xu (D0SC01340D-(cit19d)/*[position()=1]) 2015; 44
Wang (D0SC01340D-(cit42)/*[position()=1]) 2020; 10
DeRosa (D0SC01340D-(cit44)/*[position()=1]) 2002; 233–234
Shaw (D0SC01340D-(cit1a)/*[position()=1]) 2016; 81
Guo (D0SC01340D-(cit8b)/*[position()=1]) 2016; 55
Hill (D0SC01340D-(cit10a)/*[position()=1]) 1995
Wu (D0SC01340D-(cit9a)/*[position()=1]) 2004; 62
Tzirakis (D0SC01340D-(cit10e)/*[position()=1]) 2009; 131
Zhang (D0SC01340D-(cit4b)/*[position()=1]) 2018; 140
To (D0SC01340D-(cit16)/*[position()=1]) 2017; 56
Miyaura (D0SC01340D-(cit19a)/*[position()=1]) 1995; 95
Cetin (D0SC01340D-(cit2g)/*[position()=1]) 2017; 46
Srivastava (D0SC01340D-(cit17)/*[position()=1]) 1999; 34
Yang (D0SC01340D-(cit10v)/*[position()=1]) 2019; 9
Glaser (D0SC01340D-(cit43c)/*[position()=1]) 2020; 59
Quattrini (D0SC01340D-(cit10o)/*[position()=1]) 2017; 53
Poelma (D0SC01340D-(cit34e)/*[position()=1]) 2016; 81
Okamoto (D0SC01340D-(cit36c)/*[position()=1]) 2016; 52
Okada (D0SC01340D-(cit10h)/*[position()=1]) 2014; 5
Li (D0SC01340D-(cit2c)/*[position()=1]) 1992
Ghosh (D0SC01340D-(cit43a)/*[position()=1]) 2014; 346
Stevenson (D0SC01340D-(cit6d)/*[position()=1]) 2017; 8
Dietrich-Buchecker (D0SC01340D-(cit2a)/*[position()=1]) 1983
Suzuki (D0SC01340D-(cit19b)/*[position()=1]) 2011; 50
Qiao (D0SC01340D-(cit8i)/*[position()=1]) 2018; 57
Higgins (D0SC01340D-(cit6b)/*[position()=1]) 2016; 138
Kern (D0SC01340D-(cit2b)/*[position()=1]) 1987
Zhang (D0SC01340D-(cit22a)/*[position()=1]) 2017; 139
Kjær (D0SC01340D-(cit7b)/*[position()=1]) 2019; 363
Suzuki (D0SC01340D-(cit9e)/*[position()=1]) 2018; 8
Murarka (D0SC01340D-(cit26f)/*[position()=1]) 2018; 360
Fallon (D0SC01340D-(cit32c)/*[position()=1]) 2016; 40
Kong (D0SC01340D-(cit35)/*[position()=1]) 2018; 20
Okada (D0SC01340D-(cit27)/*[position()=1]) 1993; 22
Capaldo (D0SC01340D-(cit40a)/*[position()=1]) 2019; 58
Chan (D0SC01340D-(cit15)/*[position()=1]) 2019; 58
Chen (D0SC01340D-(cit20a)/*[position()=1]) 2016; 3
Cowper (D0SC01340D-(cit40d)/*[position()=1]) 2020; 142
Knorn (D0SC01340D-(cit2f)/*[position()=1]) 2015; 5
Yin (D0SC01340D-(cit8a)/*[position()=1]) 2015; 137
Yeung (D0SC01340D-(cit13)/*[position()=1]) 2017; 56
Ma (D0SC01340D-(cit36a)/*[position()=1]) 2011; 52
Sato (D0SC01340D-(cit32d)/*[position()=1]) 2014; 16
Duncan (D0SC01340D-(cit11)/*[position()=1]) 1995; 34
McAtee (D0SC01340D-(cit1h)/*[position()=1]) 2019; 1
Gualandi (D0SC01340D-(cit36d)/*[position()=1]) 2018; 54
Nakajima (D0SC01340D-(cit36b)/*[position()=1]) 2015; 54
Liu (D0SC01340D-(cit1b)/*[position()=1]) 2017; 4
Kerzig (D0SC01340D-(cit43b)/*[position()=1]) 2019; 10
Kunkely (D0SC01340D-(cit3h)/*[position()=1]) 2000; 3
Mfuh (D0SC01340D-(cit20d)/*[position()=1]) 2016; 138
Michelet (D0SC01340D-(cit34f)/*[position()=1]) 2017; 19
Tzirakis (D0SC01340D-(cit10f)/*[position()=1]) 2010; 49
Sattler (D0SC01340D-(cit12c)/*[position()=1]) 2015; 137
Jiang (D0SC01340D-(cit21a)/*[position()=1]) 2016; 18
Connell (D0SC01340D-(cit39)/*[position()=1]) 2019; 141
Cheng (D0SC01340D-(cit18b)/*[position()=1]) 2014; 5
Wang (D0SC01340D-(cit2e)/*[position()=1]) 2015; 21
Mann (D0SC01340D-(cit12b)/*[position()=1]) 1977; 99
Nitelet (D0SC01340D-(cit21b)/*[position()=1]) 2019; 25
Hu (D0SC01340D-(cit8g)/*[position()=1]) 2018; 361
Grubel (D0SC01340D-(cit3a)/*[position()=1]) 2018; 9
Gualandi (D0SC01340D-(cit7c)/*[position()=1]) 2015; 5
Halperin (D0SC01340D-(cit10i)/*[position()=1]) 2015; 17
Otto (D0SC01340D-(cit6c)/*[position()=1]) 2017; 1
Hockin (D0SC01340D-(cit1j)/*[position()=1]) 2019; 9
Laudadio (D0SC01340D-(cit10q)/*[position()=1]) 2018; 57
Fukuzumi (D0SC01340D-(cit25a)/*[position()=1]) 1990; 94
Kohlmann (D0SC01340D-(cit36e)/*[position()=1]) 2019; 25
Halperin (D0SC01340D-(cit10g)/*[position()=1]) 2014; 53
Fensterbank (D0SC01340D-(cit1e)/*[position()=1]) 2018
West (D0SC01340D-(cit10j)/*[position()=1]) 2015; 6
Revol (D0SC01340D-(cit34b)/*[position()=1]) 2013; 52
Maldotti (D0SC01340D-(cit10d)/*[position()=1]) 2008; 253
Steiner (D0SC01340D-(cit34i)/*[position()=1]) 2019
Hu (D0SC01340D-(cit8e)/*[position()=1]) 2018; 140
Wang (D0SC01340D-(cit33)/*[position()=1]) 2017; 139
Mfuh (D0SC01340D-(cit20c)/*[position()=1]) 2016; 138
Stevenson (D0SC01340D-(cit6a)/*[position()=1]) 2015; 54
Saberi (D0SC01340D-(cit37)/*[position()=1]) 2018; 106
Chen (D0SC01340D-(cit9b)/*[position()=1]) 2005; 26
To (D0SC01340D-(cit18a)/*[position()=1]) 2013; 52
Liu (D0SC01340D-(cit20e)/*[position()=1]) 2017; 139
Mao (D0SC01340D-(cit31)/*[position()=1]) 2018; 57
Wang (D0SC01340D-(cit32a)/*[position()=1]) 2018; 360
Maldotti (D0SC01340D-(cit10b)/*[position()=1]) 1997; 256
Li (D0SC01340D-(cit14)/*[position()=1]) 2018; 57
Yin (D0SC01340D-(cit8c)/*[position()=1]) 2016; 138
Zhang (D0SC01340D-(cit4a)/*[position()=1]) 2016; 138
Connell (D0SC01340D-(cit34h)/*[position()=1]) 2019; 141
Parasram (D0SC01340D-(cit1c)/*[position()=1]) 2017; 46
Lim (D0SC01340D-(cit3d)/*[position()=1]) 2018; 140
Mann (D0SC01340D-(cit12a)/*[position()=1]) 1976; 16
Förster (D0SC01340D-(cit1k)/*[position()=1]) 2020; 49
Hu (D0SC01340D-(cit8f)/*[position()=1]) 2018; 140
Yan (D0SC01340D-(cit40c)/*[position()=1]) 2019; 58
Zlotorzynska (D0SC01340D-(cit26c)/*[position()=1]) 2011; 13
Dondi (D0SC01340D-(cit10c)/*[position()=1]) 2004; 10
Senaweera (D0SC01340D-(cit34c)/*[position()=1]) 2014; 136
Perry (D0SC01340D-(cit10s)/*[position()=1]) 2018; 560
Yamada (D0SC01340D-(cit10k)/*[position()=1]) 2015; 17
Huang (D0SC01340D-(cit40b)/*[position()=1]) 2019; 58
Jenks (D0SC01340D-(cit8h)/*[position()=1]) 2018; 9
Schultz (D0SC01340D-(cit10p)/*[position()=1]) 2017; 56
Jung (D0SC01340D-(cit25b)/*[position()=1]) 2016; 358
Zhang (D0SC01340D-(cit22b)/*[position()=1]) 2019; 141
Schwarz (D0SC01340D-(cit26e)/*[position()=1]) 2016; 18
Glaser (D0SC01340D-(cit1i)/*[position()=1]) 2020; 405
Zou (D0SC01340D-(cit45b)/*[position()=1]) 2012; 51
Otto, S (WOS:000407646800001) 2017; 1
Sattler, W (WOS:000348690100031) 2015; 137
Chen, K (WOS:000377262200024) 2016; 7
Chen, Z. (000544484900023.11) 2005; 26
Schultz, DM (WOS:000416126600012) 2017; 56
Meanwell, M (WOS:000443170200026) 2018; 54
Hou, MM (WOS:000477947800003) 2019; 10
Haring, M (WOS:000365014400025) 2015; 51
Zhang, L (WOS:000475540800002) 2019; 141
Wang, ZJ (WOS:000426489300016) 2018; 360
Xu, L (WOS:000365530400007) 2015; 44
MANN, KR (WOS:A1977CR84000083) 1977; 99
Yin, HL (WOS:000358896600010) 2015; 137
Maldotti, A (WOS:A1997WY49400021) 1997; 256
Kjmer, KS (WOS:000456140700029) 2019; 363
DeRosa, MC (WOS:000178841400021) 2002; 233
Halperin, SD (WOS:000364434900014) 2015; 17
Stevenson, SM (WOS:000391454500080) 2017; 8
Steiner, A (WOS:000477378900001) 2019; 2019
Quattrini, MC (WOS:000395874700007) 2017; 53
OKADA, K (WOS:A1993MM32800010) 1993
Halperin, SD (WOS:000334894100034) 2014; 53
Yin, HL (WOS:000390729500020) 2016; 138
Forster, C (WOS:000515511500008) 2020; 49
Srivastava, AM (WOS:000083944500007) 1999; 34
West, JG (WOS:000367569500006) 2015; 6
Larsen, CB (WOS:000424792600002) 2018; 24
Hu, AH (WOS:000424851500012) 2018; 140
Parasram, M (WOS:000413188900010) 2017; 46
Glaser, F (WOS:000524308600001) 2020; 59
Hockin, BM (WOS:000459893900001) 2019; 9
Yeung, KT (WOS:000394861200011) 2017; 56
Jiang, M (WOS:000386187300016) 2016; 18
Knorn, M (WOS:000361089700026) 2015; 5
OKADA, K (WOS:A1989AZ87300028) 1989
Chow, PK (WOS:000349391000010) 2015; 54
Fallon, BJ (WOS:000390724600006) 2016; 40
West, JG (WOS:000398822700010) 2017; 57
Kim, H (WOS:000311706500030) 2012; 51
Kim, H (WOS:000512222700001) 2020; 142
Hu, AH (WOS:000448755200013) 2018; 140
Yamaguchi, J (WOS:000308043900007) 2012; 51
Mao, RZ (WOS:000438712600051) 2018; 57
Nakajima, M (WOS:000358051600048) 2015; 54
Zhang, J (WOS:000382843700010) 2016; 8
Nitelet, A (WOS:000460679500015) 2019; 25
KERN, JM (WOS:A1987H063800012) 1987
Wallentin, CJ (WOS:000304570700030) 2012; 134
OKADA, K (WOS:A1988R625200047) 1988; 110
Kong, WG (WOS:000423252400009) 2018; 20
Kerzig, C (WOS:000502319900004) 2019; 10
Chen, K (WOS:000382496400016) 2016; 3
Murphy, JJ (WOS:000374415100036) 2016; 532
Bardagi, JI (WOS:000419707900004) 2018; 2018
Jung, J (WOS:000370256000011) 2016; 358
Kim, SH (WOS:000086603800008) 2000; 65
DIETRICHBUCHECKER, CO (WOS:A1983QN82300024) 1983
Shen, X (WOS:000433426700003) 2018; 9
Capaldo, L (WOS:000494210300001) 2019; 58
Suzuki, A (WOS:000292774200004) 2011; 50
Li, K (WOS:000447371500024) 2018; 57
Okada, M (WOS:000337108200041) 2014; 5
MANN, KR (WOS:A1976BB03400014) 1976; 16
To, WP (WOS:000413896400020) 2017; 56
Stevenson, SM (WOS:000355229800017) 2015; 54
Zou, YQ (WOS:000293767000044) 2011; 50
Laudadio, G (WOS:000428350200039) 2018; 57
Sha, WX (WOS:000441112400070) 2018; 8
Cetin, MM (WOS:000401936700009) 2017; 46
Abrams, DJ (WOS:000395906900031) 2017; 8
Liu, WB (WOS:000404809600037) 2017; 139
Qiao, YS (WOS:000442863700036) 2018; 57
LI, D (WOS:A1992KC00900007) 1992
Takematsu, K (WOS:000412765000006) 2017; 46
MIYAURA, N (WOS:A1995TD89200007) 1995; 95
Cheng, G (WOS:000344376400034) 2014; 5
Zlotorzynska, M (WOS:000297274700033) 2011; 13
Yin, HL (WOS:000375889100040) 2016; 138
Zhang, Y (WOS:000385469600005) 2016; 138
Yuan, ZL (WOS:000485090400064) 2019; 9
Wu, YQ (WOS:000222218900008) 2004; 62
Shields, BJ (WOS:000426617700049) 2018; 140
Ghosh, I (WOS:000344690100034) 2014; 346
HIRONAKA, K (WOS:A1984TN99400019) 1984
Cismesia, MA (WOS:000361212000009) 2015; 6
Marzo, L (WOS:000440135700004) 2018; 57
FUKUZUMI, S (WOS:A1990CL43800039) 1990; 94
Wang, DH (WOS:000415028200020) 2017; 139
Perry, IB (WOS:000440552600045) 2018; 560
Kohlmann, T (WOS:000476918500027) 2019; 25
Yan, H (WOS:000462622700023) 2019; 58
Park, G (WOS:000388471700037) 2016; 22
Zhu, XL (WOS:000456350300003) 2019; 141
Jamison, CR (WOS:000381654700014) 2016; 49
Cui, Y. (000544484900023.18) 2012
Wang, B (WOS:000347615200033) 2015; 21
Jenks, TC (WOS:000424010600021) 2018; 9
Frem, RCG (WOS:A1997WK73100008) 1997; 255
DUNCAN, DC (WOS:A1995RT11300021) 1995; 34
Huang, H (WOS:000479869100001) 2019; 58
Wang, ZZ (WOS:000506725100018) 2020; 10
Lim, CH (WOS:000436211600046) 2018; 140
Hill, C. L. (000544484900023.41) 1995; 127
Gualandi, A (WOS:000443956300046) 2018; 54
Shaw, MH (WOS:000381847600002) 2016; 81
Zhang, Y (WOS:000432091700011) 2018; 140
Mfuh, AM (WOS:000371945800029) 2016; 138
OKADA, K (WOS:A1991GQ93100074) 1991; 113
Gualandi, A (WOS:000362391500028) 2015; 5
McAtee, RC (WOS:000521129500013) 2019; 1
Glaser, F (WOS:000509626700008) 2020; 405
Poelma, SO (WOS:000381847600032) 2016; 81
Chan, KT (WOS:000395906900086) 2017; 8
Yang, HB (WOS:000471212600102) 2019; 9
Schwarz, J (WOS:000382026600017) 2016; 18
Twilton, J (WOS:000415236400002) 2017; 1
Senaweera, SM (WOS:000332144300018) 2014; 136
Herr, P (WOS:000486361800051) 2019; 141
Zhang, J (WOS:000345572400007) 2015; 53
Zou, YQ (WOS:000299034200037) 2012; 51
Tzirakis, MD (WOS:000264792700065) 2009; 131
Dondi, D (WOS:000188087800014) 2004; 10
Chabera, P (WOS:000397619700051) 2017; 543
Cowper, NGW (WOS:000512222700002) 2020; 142
Zimmer, P (WOS:000397852200011) 2017
Liu, YJ (WOS:000398188600011) 2017; 12
Higgins, RF (WOS:000375244700043) 2016; 138
Yuan, ZL (WOS:000444941600019) 2018; 57
Michelet, B (WOS:000405358300062) 2017; 19
Connell, TU (WOS:000495769300025) 2019; 141
Okamoto, S (WOS:000384203100003) 2016; 52
Tzirakis, MD (WOS:000281105600010) 2010; 49
Revol, G (WOS:000327802100039) 2013; 52
To, WP (WOS:000320733600014) 2013; 52
Malzkuhn, S (WOS:000424958800003) 2018; 359
Cuttell, DG (WOS:000173217900003) 2002; 124
Buldt, LA (WOS:000383642300053) 2016; 55
Buldt, LA (WOS:000404147500004) 2017; 23
Chan, KT (WOS:000490580800016) 2019; 58
Kunkely, H (WOS:000085911600016) 2000; 3
Fensterbank, L. (000544484900023.25) 2018
Jiang, WT (WOS:000505529100019) 2020; 11
Murarka, S (WOS:000431487200001) 2018; 360
Maldotti, A (WOS:000253282000011) 2008; 253
Hu, AH (WOS:000442818200036) 2018; 361
Liu, Q (WOS:000406611700011) 2017; 4
Nguyen, JD (WOS:000291715300003) 2011; 133
Mfuh, AM (WOS:000379794400023) 2016; 138
Meanwell, M (WOS:000385799200058) 2016; 55
Saberi, D (WOS:000423640400011) 2018; 106
Suzuki, K (WOS:000449723900093) 2018; 8
Supranovich, VI (WOS:000471212100084) 2019; 21
Sato, K (WOS:000339367300037) 2014; 16
Guo, JJ (WOS:000389224000023) 2016; 55
Yamada, K (WOS:000350841300059) 2015; 17
Zhang, L (WOS:000392459300011) 2017; 139
Ma, N (WOS:000287179900019) 2011; 52
Grubel, M (WOS:000431113300007) 2018; 9
References_xml – issn: 2012
  publication-title: Preparation of tungsten trioxide photocatalyst and its Application
  doi: Cui Li Zhang
– issn: 2018
  publication-title: Visible Light Photocatalysis in Organic Chemistry
  doi: Fensterbank Goddard Ollivier
– volume: 361
  start-page: 668
  year: 2018
  ident: D0SC01340D-(cit8g)/*[position()=1]
  publication-title: Science
  doi: 10.1126/science.aat9750
– volume: 53
  start-page: 42
  year: 2015
  ident: D0SC01340D-(cit7d)/*[position()=1]
  publication-title: J. Polym. Sci., Part A: Polym. Chem.
  doi: 10.1002/pola.27435
– volume: 54
  start-page: 2084
  year: 2015
  ident: D0SC01340D-(cit18c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201408940
– volume: 49
  start-page: 5891
  year: 2010
  ident: D0SC01340D-(cit10f)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201002285
– volume: 53
  start-page: 2335
  year: 2017
  ident: D0SC01340D-(cit10o)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC09725A
– volume: 233–234
  start-page: 351
  year: 2002
  ident: D0SC01340D-(cit44)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/S0010-8545(02)00034-6
– volume: 141
  start-page: 17646
  year: 2019
  ident: D0SC01340D-(cit34h)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b07370
– start-page: 5807
  year: 2019
  ident: D0SC01340D-(cit34i)/*[position()=1]
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201900952
– volume: 405
  start-page: 213129
  year: 2020
  ident: D0SC01340D-(cit1i)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2019.213129
– volume: 65
  start-page: 2322
  year: 2000
  ident: D0SC01340D-(cit32e)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/jo991478s
– volume: 560
  start-page: 70
  year: 2018
  ident: D0SC01340D-(cit10s)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/s41586-018-0366-x
– volume: 8
  start-page: 2227
  year: 2016
  ident: D0SC01340D-(cit7e)/*[position()=1]
  publication-title: ChemCatChem
  doi: 10.1002/cctc.201600320
– volume: 58
  start-page: 13318
  year: 2019
  ident: D0SC01340D-(cit40b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201906381
– volume: 62
  start-page: 1134
  year: 2004
  ident: D0SC01340D-(cit9a)/*[position()=1]
  publication-title: Acta Chim. Sin.
– volume: 256
  start-page: 309
  year: 1997
  ident: D0SC01340D-(cit10b)/*[position()=1]
  publication-title: Inorg. Chim. Acta
  doi: 10.1016/S0020-1693(96)05432-1
– volume: 4
  start-page: 359
  year: 2017
  ident: D0SC01340D-(cit1b)/*[position()=1]
  publication-title: Natl. Sci. Rev.
  doi: 10.1093/nsr/nwx039
– volume: 141
  start-page: 9124
  year: 2019
  ident: D0SC01340D-(cit22b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b00917
– volume: 1
  start-page: 111
  year: 2019
  ident: D0SC01340D-(cit1h)/*[position()=1]
  publication-title: Trends Chem.
  doi: 10.1016/j.trechm.2019.01.008
– volume: 51
  start-page: 16848
  year: 2015
  ident: D0SC01340D-(cit34d)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC06917C
– volume: 58
  start-page: 17508
  year: 2019
  ident: D0SC01340D-(cit40a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201910348
– volume: 3
  start-page: 875
  year: 2016
  ident: D0SC01340D-(cit20a)/*[position()=1]
  publication-title: Org. Chem. Front.
  doi: 10.1039/C6QO00109B
– volume: 81
  start-page: 7155
  year: 2016
  ident: D0SC01340D-(cit34e)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.6b01034
– volume: 59
  year: 2020
  ident: D0SC01340D-(cit43c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201915762
– volume: 16
  start-page: 97
  year: 1976
  ident: D0SC01340D-(cit12a)/*[position()=1]
  publication-title: Inorg. Chim. Acta
  doi: 10.1016/S0020-1693(00)91697-9
– start-page: 546
  year: 1987
  ident: D0SC01340D-(cit2b)/*[position()=1]
  publication-title: J. Chem. Soc., Chem. Commun.
  doi: 10.1039/C39870000546
– volume: 55
  start-page: 13244
  year: 2016
  ident: D0SC01340D-(cit10l)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201606323
– volume-title: Preparation of tungsten trioxide photocatalyst and its Application
  year: 2012
  ident: D0SC01340D-(cit9c)/*[position()=1]
– volume: 24
  start-page: 2039
  year: 2018
  ident: D0SC01340D-(cit1f)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201703602
– volume: 359
  start-page: 52
  year: 2018
  ident: D0SC01340D-(cit3c)/*[position()=1]
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2018.01.003
– volume: 9
  start-page: 5708
  year: 2019
  ident: D0SC01340D-(cit10v)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b01394
– volume: 22
  start-page: 17790
  year: 2016
  ident: D0SC01340D-(cit24)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201603517
– volume: 11
  start-page: 488
  year: 2020
  ident: D0SC01340D-(cit30)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C9SC04288A
– volume: 58
  start-page: 4592
  year: 2019
  ident: D0SC01340D-(cit40c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201814488
– volume: 81
  start-page: 6898
  year: 2016
  ident: D0SC01340D-(cit1a)/*[position()=1]
  publication-title: J. Org. Chem.
  doi: 10.1021/acs.joc.6b01449
– volume: 10
  start-page: 142
  year: 2004
  ident: D0SC01340D-(cit10c)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.200305285
– volume: 94
  start-page: 722
  year: 1990
  ident: D0SC01340D-(cit25a)/*[position()=1]
  publication-title: J. Phys. Chem.
  doi: 10.1021/j100365a039
– volume: 51
  start-page: 784
  year: 2012
  ident: D0SC01340D-(cit45b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201107028
– volume: 346
  start-page: 725
  year: 2014
  ident: D0SC01340D-(cit43a)/*[position()=1]
  publication-title: Science
  doi: 10.1126/science.1258232
– volume: 13
  start-page: 6264
  year: 2011
  ident: D0SC01340D-(cit26c)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol202740w
– start-page: 127
  year: 1995
  ident: D0SC01340D-(cit10a)/*[position()=1]
  publication-title: Synlett
  doi: 10.1055/s-1995-4883
– volume: 140
  start-page: 7667
  year: 2018
  ident: D0SC01340D-(cit3d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b03744
– volume: 255
  start-page: 53
  year: 1997
  ident: D0SC01340D-(cit3g)/*[position()=1]
  publication-title: Inorg. Chim. Acta
  doi: 10.1016/S0020-1693(96)05335-2
– volume: 52
  start-page: 11339
  year: 2016
  ident: D0SC01340D-(cit36c)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C6CC05867A
– volume: 532
  start-page: 218
  year: 2016
  ident: D0SC01340D-(cit10m)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/nature17438
– volume: 5
  start-page: 5186
  year: 2015
  ident: D0SC01340D-(cit2f)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.5b01071
– volume: 1
  start-page: 0052
  year: 2017
  ident: D0SC01340D-(cit1d)/*[position()=1]
  publication-title: Nat. Rev. Chem.
  doi: 10.1038/s41570-017-0052
– volume: 113
  start-page: 9401
  year: 1991
  ident: D0SC01340D-(cit26b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00024a074
– volume: 52
  start-page: 718
  year: 2011
  ident: D0SC01340D-(cit36a)/*[position()=1]
  publication-title: Tetrahedron Lett.
  doi: 10.1016/j.tetlet.2010.12.007
– volume: 54
  start-page: 8828
  year: 2015
  ident: D0SC01340D-(cit36b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201501556
– volume: 360
  start-page: 1735
  year: 2018
  ident: D0SC01340D-(cit26f)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701615
– volume: 141
  start-page: 733
  year: 2019
  ident: D0SC01340D-(cit25d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b08720
– volume: 10
  start-page: 6629
  year: 2019
  ident: D0SC01340D-(cit25c)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C9SC02000D
– volume: 9
  start-page: 4562
  year: 2018
  ident: D0SC01340D-(cit3e)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C8SC01219A
– volume: 138
  start-page: 2985
  year: 2016
  ident: D0SC01340D-(cit20c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b01376
– volume: 21
  start-page: 1184
  year: 2015
  ident: D0SC01340D-(cit2e)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201405356
– volume: 9
  start-page: 889
  year: 2019
  ident: D0SC01340D-(cit1j)/*[position()=1]
  publication-title: Catal. Sci. Technol.
  doi: 10.1039/C8CY02336K
– volume: 138
  start-page: 5451
  year: 2016
  ident: D0SC01340D-(cit6b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b02723
– volume: 6
  start-page: 5426
  year: 2015
  ident: D0SC01340D-(cit41)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C5SC02185E
– volume: 140
  start-page: 13580
  year: 2018
  ident: D0SC01340D-(cit8e)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b08781
– volume: 141
  start-page: 17646
  year: 2019
  ident: D0SC01340D-(cit39)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b07370
– volume: 53
  start-page: 4690
  year: 2014
  ident: D0SC01340D-(cit10g)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201400420
– volume: 26
  start-page: 57
  year: 2005
  ident: D0SC01340D-(cit9b)/*[position()=1]
  publication-title: J. Jiangsu Univ.
– volume: 5
  start-page: 4819
  year: 2014
  ident: D0SC01340D-(cit18b)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C4SC01105H
– volume: 253
  start-page: 312
  year: 2008
  ident: D0SC01340D-(cit10d)/*[position()=1]
  publication-title: J. Catal.
  doi: 10.1016/j.jcat.2007.11.008
– volume: 44
  start-page: 8848
  year: 2015
  ident: D0SC01340D-(cit19d)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C5CS00338E
– volume: 10
  start-page: 154
  year: 2020
  ident: D0SC01340D-(cit42)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b04411
– volume: 46
  start-page: 6227
  year: 2017
  ident: D0SC01340D-(cit1c)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C7CS00226B
– volume: 9
  start-page: 8276
  year: 2019
  ident: D0SC01340D-(cit9f)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.9b02220
– volume: 54
  start-page: 6506
  year: 2015
  ident: D0SC01340D-(cit6a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201501220
– volume: 134
  start-page: 8875
  year: 2012
  ident: D0SC01340D-(cit38b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja300798k
– volume: 54
  start-page: 9985
  year: 2018
  ident: D0SC01340D-(cit10r)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC06375C
– volume: 360
  start-page: 932
  year: 2018
  ident: D0SC01340D-(cit32a)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201701389
– volume: 8
  start-page: 1954
  year: 2017
  ident: D0SC01340D-(cit10n)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC04607J
– volume: 56
  start-page: 15274
  year: 2017
  ident: D0SC01340D-(cit10p)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201707537
– start-page: 34
  year: 2018
  ident: D0SC01340D-(cit34g)/*[position()=1]
  publication-title: Eur. J. Org. Chem.
  doi: 10.1002/ejoc.201701461
– volume: 58
  start-page: 14896
  year: 2019
  ident: D0SC01340D-(cit15)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201906698
– volume: 106
  start-page: 50
  year: 2018
  ident: D0SC01340D-(cit37)/*[position()=1]
  publication-title: Catal. Commun.
  doi: 10.1016/j.catcom.2017.12.012
– volume: 358
  start-page: 74
  year: 2016
  ident: D0SC01340D-(cit25b)/*[position()=1]
  publication-title: Adv. Synth. Catal.
  doi: 10.1002/adsc.201500734
– start-page: 1705
  year: 1984
  ident: D0SC01340D-(cit23)/*[position()=1]
  publication-title: J. Chem. Soc., Perkin Trans. 2
  doi: 10.1039/p29840001705
– volume: 19
  start-page: 3576
  year: 2017
  ident: D0SC01340D-(cit34f)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.7b01518
– volume: 55
  start-page: 15319
  year: 2016
  ident: D0SC01340D-(cit8b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201609035
– volume: 17
  start-page: 1292
  year: 2015
  ident: D0SC01340D-(cit10k)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b00282
– volume: 9
  start-page: 3313
  year: 2018
  ident: D0SC01340D-(cit3a)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C7SC05320G
– volume: 138
  start-page: 16266
  year: 2016
  ident: D0SC01340D-(cit8d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b05712
– volume: 46
  start-page: 13188
  year: 2017
  ident: D0SC01340D-(cit12d)/*[position()=1]
  publication-title: Dalton Trans.
  doi: 10.1039/C7DT02632C
– volume: 142
  start-page: 2093
  year: 2020
  ident: D0SC01340D-(cit40d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b12328
– volume: 5
  start-page: 2893
  year: 2014
  ident: D0SC01340D-(cit10h)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C4SC01072H
– volume: 34
  start-page: 1397
  year: 1999
  ident: D0SC01340D-(cit17)/*[position()=1]
  publication-title: Mater. Res. Bull.
  doi: 10.1016/S0025-5408(99)00148-8
– volume: 138
  start-page: 8408
  year: 2016
  ident: D0SC01340D-(cit20d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b05436
– volume: 57
  start-page: 9501
  year: 2018
  ident: D0SC01340D-(cit31)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201804873
– volume: 17
  start-page: 5200
  year: 2015
  ident: D0SC01340D-(cit10i)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.5b02532
– volume: 57
  start-page: 12733
  year: 2018
  ident: D0SC01340D-(cit10t)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201806966
– volume: 3
  start-page: 143
  year: 2000
  ident: D0SC01340D-(cit3h)/*[position()=1]
  publication-title: Inorg. Chem. Commun.
  doi: 10.1016/S1387-7003(00)00034-4
– volume: 133
  start-page: 4160
  year: 2011
  ident: D0SC01340D-(cit38a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja108560e
– volume: 95
  start-page: 2457
  year: 1995
  ident: D0SC01340D-(cit19a)/*[position()=1]
  publication-title: Chem. Rev.
  doi: 10.1021/cr00039a007
– volume: 141
  start-page: 14394
  year: 2019
  ident: D0SC01340D-(cit5b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.9b07373
– volume: 138
  start-page: 5984
  year: 2016
  ident: D0SC01340D-(cit8c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b02248
– volume: 9
  start-page: 1273
  year: 2018
  ident: D0SC01340D-(cit8h)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C7SC02479G
– volume: 139
  start-page: 15632
  year: 2017
  ident: D0SC01340D-(cit33)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b09802
– start-page: 1636
  year: 1989
  ident: D0SC01340D-(cit29)/*[position()=1]
  publication-title: J. Chem. Soc., Chem. Commun.
  doi: 10.1039/c39890001636
– start-page: 513
  year: 1983
  ident: D0SC01340D-(cit2a)/*[position()=1]
  publication-title: J. Chem. Soc., Chem. Commun.
  doi: 10.1039/c39830000513
– volume: 363
  start-page: 249
  year: 2019
  ident: D0SC01340D-(cit7b)/*[position()=1]
  publication-title: Science
  doi: 10.1126/science.aau7160
– start-page: 3325
  year: 1992
  ident: D0SC01340D-(cit2c)/*[position()=1]
  publication-title: J. Chem. Soc., Dalton Trans.
  doi: 10.1039/DT9920003325
– volume: 57
  start-page: 10999
  year: 2018
  ident: D0SC01340D-(cit8i)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201804022
– volume: 57
  start-page: 4078
  year: 2018
  ident: D0SC01340D-(cit10q)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201800818
– volume: 140
  start-page: 3035
  year: 2018
  ident: D0SC01340D-(cit3f)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b13281
– volume: 46
  start-page: 6553
  year: 2017
  ident: D0SC01340D-(cit2g)/*[position()=1]
  publication-title: Dalton Trans.
  doi: 10.1039/C7DT00400A
– volume: 40
  start-page: 9912
  year: 2016
  ident: D0SC01340D-(cit32c)/*[position()=1]
  publication-title: New J. Chem.
  doi: 10.1039/C6NJ03265F
– volume: 56
  start-page: 133
  year: 2017
  ident: D0SC01340D-(cit13)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201608240
– start-page: 1504
  year: 2017
  ident: D0SC01340D-(cit7f)/*[position()=1]
  publication-title: Eur. J. Inorg. Chem.
  doi: 10.1002/ejic.201700064
– volume: 18
  start-page: 4743
  year: 2016
  ident: D0SC01340D-(cit26e)/*[position()=1]
  publication-title: Green Chem.
  doi: 10.1039/C6GC01101B
– volume: 12
  start-page: 673
  year: 2017
  ident: D0SC01340D-(cit32b)/*[position()=1]
  publication-title: Chem.–Asian J.
  doi: 10.1002/asia.201601712
– volume: 139
  start-page: 607
  year: 2017
  ident: D0SC01340D-(cit22a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b11813
– volume: 99
  start-page: 306
  year: 1977
  ident: D0SC01340D-(cit12b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00443a083
– volume: 51
  start-page: 8960
  year: 2012
  ident: D0SC01340D-(cit19c)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201201666
– volume: 52
  start-page: 13342
  year: 2013
  ident: D0SC01340D-(cit34b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201306727
– volume: 137
  start-page: 1198
  year: 2015
  ident: D0SC01340D-(cit12c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja510973h
– volume: 22
  start-page: 2021
  year: 1993
  ident: D0SC01340D-(cit27)/*[position()=1]
  publication-title: Chem. Lett.
  doi: 10.1246/cl.1993.2021
– volume: 16
  start-page: 3756
  year: 2014
  ident: D0SC01340D-(cit32d)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/ol501619w
– volume: 57
  start-page: 14129
  year: 2018
  ident: D0SC01340D-(cit14)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201808642
– volume: 10
  start-page: 11023
  year: 2019
  ident: D0SC01340D-(cit43b)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C9SC04584H
– volume: 140
  start-page: 1612
  year: 2018
  ident: D0SC01340D-(cit8f)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b13131
– volume: 8
  start-page: 10809
  year: 2018
  ident: D0SC01340D-(cit9e)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.8b03498
– volume: 55
  start-page: 11247
  year: 2016
  ident: D0SC01340D-(cit5a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201605571
– volume: 18
  start-page: 5248
  year: 2016
  ident: D0SC01340D-(cit21a)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.6b02553
– volume: 56
  start-page: 14036
  year: 2017
  ident: D0SC01340D-(cit16)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201707193
– volume: 137
  start-page: 9234
  year: 2015
  ident: D0SC01340D-(cit8a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.5b05411
– volume: 25
  start-page: 9991
  year: 2019
  ident: D0SC01340D-(cit36e)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201901618
– volume: 8
  start-page: 654
  year: 2017
  ident: D0SC01340D-(cit6d)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC03303B
– volume: 139
  start-page: 8621
  year: 2017
  ident: D0SC01340D-(cit20e)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b03538
– volume: 20
  start-page: 349
  year: 2018
  ident: D0SC01340D-(cit35)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.7b03587
– volume: 142
  start-page: 2087
  year: 2020
  ident: D0SC01340D-(cit40e)/*[position()=1]
  publication-title: J. Am. Chem. Soc. Chem
  doi: 10.1021/jacs.9b10678
– volume: 21
  start-page: 4271
  year: 2019
  ident: D0SC01340D-(cit10u)/*[position()=1]
  publication-title: Org. Lett.
  doi: 10.1021/acs.orglett.9b01450
– volume: 136
  start-page: 3002
  year: 2014
  ident: D0SC01340D-(cit34c)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja500031m
– volume: 124
  start-page: 6
  year: 2002
  ident: D0SC01340D-(cit2d)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja012247h
– volume: 51
  start-page: 12303
  year: 2012
  ident: D0SC01340D-(cit34a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201203599
– volume: 52
  start-page: 6648
  year: 2013
  ident: D0SC01340D-(cit18a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201301149
– volume: 57
  start-page: 259
  year: 2017
  ident: D0SC01340D-(cit9d)/*[position()=1]
  publication-title: Isr. J. Chem.
  doi: 10.1002/ijch.201600115
– volume: 25
  start-page: 3262
  year: 2019
  ident: D0SC01340D-(cit21b)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201806345
– volume: 8
  start-page: 2352
  year: 2017
  ident: D0SC01340D-(cit18d)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C6SC03775E
– volume: 110
  start-page: 8736
  year: 1988
  ident: D0SC01340D-(cit26a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00234a047
– volume: 131
  start-page: 4063
  year: 2009
  ident: D0SC01340D-(cit10e)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja808658b
– volume: 7
  start-page: 3676
  year: 2016
  ident: D0SC01340D-(cit20b)/*[position()=1]
  publication-title: Chem. Sci.
  doi: 10.1039/C5SC04521E
– volume: 1
  start-page: 344
  year: 2017
  ident: D0SC01340D-(cit6c)/*[position()=1]
  publication-title: ChemPhotoChem
  doi: 10.1002/cptc.201700077
– volume: 49
  start-page: 1578
  year: 2016
  ident: D0SC01340D-(cit26d)/*[position()=1]
  publication-title: Acc. Chem. Res.
  doi: 10.1021/acs.accounts.6b00284
– volume: 54
  start-page: 10044
  year: 2018
  ident: D0SC01340D-(cit36d)/*[position()=1]
  publication-title: Chem. Commun.
  doi: 10.1039/C8CC04048F
– volume-title: Visible Light Photocatalysis in Organic Chemistry
  year: 2018
  ident: D0SC01340D-(cit1e)/*[position()=1]
– volume: 8
  start-page: 7489
  year: 2018
  ident: D0SC01340D-(cit28)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.8b01863
– volume: 138
  start-page: 13115
  year: 2016
  ident: D0SC01340D-(cit4a)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.6b05934
– volume: 23
  start-page: 8577
  year: 2017
  ident: D0SC01340D-(cit3b)/*[position()=1]
  publication-title: Chem. – Eur. J.
  doi: 10.1002/chem.201700103
– volume: 50
  start-page: 7171
  year: 2011
  ident: D0SC01340D-(cit45a)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201102306
– volume: 50
  start-page: 6722
  year: 2011
  ident: D0SC01340D-(cit19b)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201101379
– volume: 34
  start-page: 4640
  year: 1995
  ident: D0SC01340D-(cit11)/*[position()=1]
  publication-title: Inorg. Chem.
  doi: 10.1021/ic00122a021
– volume: 49
  start-page: 1057
  year: 2020
  ident: D0SC01340D-(cit1k)/*[position()=1]
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00573K
– volume: 140
  start-page: 5934
  year: 2018
  ident: D0SC01340D-(cit4b)/*[position()=1]
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.8b00742
– volume: 5
  start-page: 5927
  year: 2015
  ident: D0SC01340D-(cit7c)/*[position()=1]
  publication-title: ACS Catal.
  doi: 10.1021/acscatal.5b01573
– volume: 6
  start-page: 10093
  year: 2015
  ident: D0SC01340D-(cit10j)/*[position()=1]
  publication-title: Nat. Commun.
  doi: 10.1038/ncomms10093
– volume: 57
  start-page: 10034
  year: 2018
  ident: D0SC01340D-(cit1g)/*[position()=1]
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.201709766
– volume: 543
  start-page: 695
  year: 2017
  ident: D0SC01340D-(cit7a)/*[position()=1]
  publication-title: Nature
  doi: 10.1038/nature21430
– volume: 58
  start-page: 4592
  year: 2019
  ident: WOS:000462622700023
  article-title: Photoelectrochemical C-H Alkylation of Heteroarenes with Organotrifluoroborates
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201814488
– volume: 22
  start-page: 17790
  year: 2016
  ident: WOS:000388471700037
  article-title: Mechanism and Applications of the Photoredox Catalytic Coupling of Benzyl Bromides
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201603517
– volume: 12
  start-page: 673
  year: 2017
  ident: WOS:000398188600011
  article-title: Reductive Homocoupling of Organohalides Using Nickel(II) Chloride and Samarium Metal
  publication-title: CHEMISTRY-AN ASIAN JOURNAL
  doi: 10.1002/asia.201601712
– volume: 134
  start-page: 8875
  year: 2012
  ident: WOS:000304570700030
  article-title: Visible Light-Mediated Atom Transfer Radical Addition via Oxidative and Reductive Quenching of Photocatalysts
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja300798k
– volume: 2018
  start-page: 34
  year: 2018
  ident: WOS:000419707900004
  article-title: Anthraquinones as Photoredox Catalysts for the Reductive Activation of Aryl Halides
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201701461
– year: 2018
  ident: 000544484900023.25
  publication-title: Visible Light Photocatalysis in Organic Chemistry
– volume: 65
  start-page: 2322
  year: 2000
  ident: WOS:000086603800008
  article-title: Benzylic manganese halides, sulfonates, and phosphates: Preparation, coupling reactions, and applications in organic synthesis
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
– volume: 9
  start-page: 1273
  year: 2018
  ident: WOS:000424010600021
  article-title: First use of a divalent lanthanide for visible-light-promoted photoredox catalysis
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c7sc02479g
– volume: 21
  start-page: 1184
  year: 2015
  ident: WOS:000347615200033
  article-title: Long-Lived Excited States of Zwitterionic Copper(I) Complexes for Photoinduced Cross-Dehydrogenative Coupling Reactions
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201405356
– volume: 5
  start-page: 4819
  year: 2014
  ident: WOS:000344376400034
  article-title: Structurally robust phosphorescent [Pt(ONCN)] emitters for high performance organic light-1
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c4sc01105h
– volume: 49
  start-page: 1578
  year: 2016
  ident: WOS:000381654700014
  article-title: Fragment Coupling with Tertiary Radicals Generated by Visible-Light Photocatalysis
  publication-title: ACCOUNTS OF CHEMICAL RESEARCH
  doi: 10.1021/acs.accounts.6b00284
– volume: 2019
  start-page: 5807
  year: 2019
  ident: WOS:000477378900001
  article-title: Implementing Hydrogen Atom Transfer (HAT) Catalysis for Rapid and Selective Reductive Photoredox Transformations in Continuous Flow
  publication-title: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1002/ejoc.201900952
– volume: 99
  start-page: 306
  year: 1977
  ident: WOS:A1977CR84000083
  article-title: EXCITED-STATE REACTIVITY PATTERNS OF HEXAKISARYLISOCYANO COMPLEXES OF CHROMIUM(0), MOLYBDENUM(0), AND TUNGSTEN(0)
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– start-page: 1504
  year: 2017
  ident: WOS:000397852200011
  article-title: N-Heterocyclic Carbene Complexes of Iron as Photosensitizers for Light-Induced Water Reduction
  publication-title: EUROPEAN JOURNAL OF INORGANIC CHEMISTRY
  doi: 10.1002/ejic.201700064
– volume: 16
  start-page: 97
  year: 1976
  ident: WOS:A1976BB03400014
  article-title: ELECTRONIC-STRUCTURES AND SPECTRA OF HEXAKISPHENYLISOCYANIDE COMPLEXES OF CR(0), MO(0), W(0), MN(I), AND MN(II)
  publication-title: INORGANICA CHIMICA ACTA
– volume: 346
  start-page: 725
  year: 2014
  ident: WOS:000344690100034
  article-title: Reduction of aryl halides by consecutive visible light-induced electron transfer processes
  publication-title: SCIENCE
  doi: 10.1126/science.1258232
– volume: 50
  start-page: 7171
  year: 2011
  ident: WOS:000293767000044
  article-title: Visible-Light-Induced Oxidation/[3+2] Cycloaddition/Oxidative Aromatization Sequence: A Photocatalytic Strategy To Construct Pyrrolo[2,1-a]isoquinolines
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201102306
– volume: 46
  start-page: 6227
  year: 2017
  ident: WOS:000413188900010
  article-title: Visible light-induced transition metal-catalyzed transformations: beyond conventional photosensitizers
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c7cs00226b
– volume: 360
  start-page: 1735
  year: 2018
  ident: WOS:000431487200001
  article-title: N-(Acyloxy)phthalimides as Redox-Active Esters in Cross-Coupling Reactions
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701615
– volume: 543
  start-page: 695
  year: 2017
  ident: WOS:000397619700051
  article-title: A low-spin Fe(III) complex with 100-ps ligand-to-metal charge transfer photoluminescence
  publication-title: NATURE
  doi: 10.1038/nature21430
– volume: 139
  start-page: 8621
  year: 2017
  ident: WOS:000404809600037
  article-title: Simple and Efficient Generation of Aryl Radicals from Aryl Triflates: Synthesis of Aryl Boronates and Aryl Iodides at Room Temperature
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.7b03538
– volume: 59
  start-page: 10266
  year: 2020
  ident: WOS:000524308600001
  article-title: Multi-Photon Excitation in Photoredox Catalysis: Concepts, Applications, Methods
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201915762
– volume: 26
  start-page: 57
  year: 2005
  ident: 000544484900023.11
  publication-title: J. Jiangsu Univ.
– volume: 137
  start-page: 1198
  year: 2015
  ident: WOS:000348690100031
  article-title: Bespoke Photoreductants: Tungsten Arylisocyanides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja510973h
– volume: 8
  start-page: 2352
  year: 2017
  ident: WOS:000395906900086
  article-title: The interplay between fluorescence and phosphorescence with luminescent gold(I) and gold(III) complexes bearing heterocyclic arylacetylide ligands
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c6sc03775e
– volume: 51
  start-page: 8960
  year: 2012
  ident: WOS:000308043900007
  article-title: C-H Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201201666
– volume: 53
  start-page: 42
  year: 2015
  ident: WOS:000345572400007
  article-title: Iron Complexes as Photoinitiators for Radical and Cationic Polymerization Through Photoredox Catalysis Processes
  publication-title: JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY
  doi: 10.1002/pola.27435
– volume: 44
  start-page: 8848
  year: 2015
  ident: WOS:000365530400007
  article-title: Boron-selective reactions as powerful tools for modular synthesis of diverse complex molecules
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c5cs00338e
– volume: 51
  start-page: 16848
  year: 2015
  ident: WOS:000365014400025
  article-title: Intragel photoreduction of aryl halides by green-to-blue upconversion under aerobic conditions
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c5cc06917c
– volume: 52
  start-page: 11339
  year: 2016
  ident: WOS:000384203100003
  article-title: Metal-free reductive coupling of C = O and C = N bonds driven by visible light: use of perylene as a simple photoredox catalyst
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc05867a
– volume: 256
  start-page: 309
  year: 1997
  ident: WOS:A1997WY49400021
  article-title: Catalytic oxygenation of cyclohexane by photoexcited (nBu(4)N)(4)W10O32: The role of radicals
  publication-title: INORGANICA CHIMICA ACTA
– volume: 133
  start-page: 4160
  year: 2011
  ident: WOS:000291715300003
  article-title: Intermolecular Atom Transfer Radical Addition to Olefins Mediated by Oxidative Quenching of Photoredox Catalysts
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja108560e
– start-page: 2021
  year: 1993
  ident: WOS:A1993MM32800010
  article-title: REDOX-MEDIATED DECARBOXYLATIVE PHOTO-PHENYLSELENENYLATION OF N-ACYLOXYPHTHALIMIDES
  publication-title: CHEMISTRY LETTERS
– volume: 7
  start-page: 3676
  year: 2016
  ident: WOS:000377262200024
  article-title: Efficient metal-free photochemical borylation of aryl halides under batch and continuous-flow conditions
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c5sc04521e
– volume: 56
  start-page: 133
  year: 2017
  ident: WOS:000394861200011
  article-title: Luminescent Tungsten(VI) Complexes: Photophysics and Applicability to Organic Light-Emitting Diodes and Photocatalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201608240
– volume: 532
  start-page: 218
  year: 2016
  ident: WOS:000374415100036
  article-title: Asymmetric catalytic formation of quaternary carbons by iminium ion trapping of radicals
  publication-title: NATURE
  doi: 10.1038/nature17438
– volume: 9
  start-page: 3313
  year: 2018
  ident: WOS:000431113300007
  article-title: Redox and photocatalytic properties of a Ni-II complex with a macrocyclic biquinazoline (Mabiq) ligand
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c7sc05320g
– volume: 138
  start-page: 13115
  year: 2016
  ident: WOS:000385469600005
  article-title: A Luminescent Zirconium(IV) Complex as a Molecular Photosensitizer for Visible Light Photoredox Catalysis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b05934
– volume: 57
  start-page: 10034
  year: 2018
  ident: WOS:000440135700004
  article-title: Visible-Light Photocatalysis: Does It Make a Difference in Organic Synthesis?
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201709766
– volume: 8
  start-page: 2227
  year: 2016
  ident: WOS:000382843700010
  article-title: Iron Complexes in Visible-Light-Sensitive Photoredox Catalysis: Effect of Ligands on Their Photoinitiation Efficiencies
  publication-title: CHEMCATCHEM
  doi: 10.1002/cctc.201600320
– volume: 5
  start-page: 2893
  year: 2014
  ident: WOS:000337108200041
  article-title: Sunlight photocatalyzed regioselective beta-alkylation and acylation of cyclopentanones
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c4sc01072h
– volume: 141
  start-page: 9124
  year: 2019
  ident: WOS:000475540800002
  article-title: Visible-Light-Induced Organocatalytic Borylation of Aryl Chlorides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b00917
– volume: 46
  start-page: 6553
  year: 2017
  ident: WOS:000401936700009
  article-title: Characterization and photocatalytic behavior of 2,9-di(aryl)-1,10-phenanthroline copper(I) complexes
  publication-title: DALTON TRANSACTIONS
  doi: 10.1039/c7dt00400a
– volume: 57
  start-page: 10999
  year: 2018
  ident: WOS:000442863700036
  article-title: Photoinduced Miyaura Borylation by a Rare-Earth-Metal Photoreductant: The Hexachlorocerate(III) Anion
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201804022
– volume: 8
  start-page: 654
  year: 2017
  ident: WOS:000391454500080
  article-title: Chromium photocatalysis: accessing structural complements to Diels-Alder adducts with electron-deficient dienophiles
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c6sc03303b
– volume: 57
  start-page: 12733
  year: 2018
  ident: WOS:000444941600019
  article-title: Site-Selective, Late-Stage C-H F-18-Fluorination on Unprotected Peptides for Positron Emission Tomography Imaging
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201806966
– volume: 361
  start-page: 668
  year: 2018
  ident: WOS:000442818200036
  article-title: Selective functionalization of methane, ethane, and higher alkanes by cerium photocatalysis
  publication-title: SCIENCE
  doi: 10.1126/science.aat9750
– volume: 50
  start-page: 6722
  year: 2011
  ident: WOS:000292774200004
  article-title: Cross-Coupling Reactions Of Organoboranes: An Easy Way To Construct C-C Bonds (Nobel Lecture)
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201101379
– volume: 405
  start-page: ARTN 213129
  year: 2020
  ident: WOS:000509626700008
  article-title: Recent progress in the development of transition-metal based photoredox catalysts
  publication-title: COORDINATION CHEMISTRY REVIEWS
  doi: 10.1016/j.ccr.2019.213129
– volume: 58
  start-page: 17508
  year: 2019
  ident: WOS:000494210300001
  article-title: Merging Photocatalysis with Electrochemistry: The Dawn of a new Alliance in Organic Synthesis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201910348
– start-page: 1636
  year: 1989
  ident: WOS:A1989AZ87300028
  article-title: PHOTOCHEMICAL CHLORODECARBOXYLATION VIA AN ELECTRON-TRANSFER MECHANISM
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
– volume: 21
  start-page: 4271
  year: 2019
  ident: WOS:000471212100084
  article-title: Radical Addition to N-Tosylimines via C-H Activation Induced by Decatungstate Photocatalyst
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.9b01450
– volume: 138
  start-page: 2985
  year: 2016
  ident: WOS:000371945800029
  article-title: Scalable, Metal- and Additive-Free, Photoinduced Borylation of Haloarenes and Quaternary Arylammonium Salts
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b01376
– volume: 8
  start-page: 1954
  year: 2017
  ident: WOS:000395906900031
  article-title: Toward a mild dehydroformylation using base-metal catalysis
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c6sc04607j
– volume: 16
  start-page: 3756
  year: 2014
  ident: WOS:000339367300037
  article-title: Csp(3)-Csp(3) Homocoupling Reaction of Benzyl Halides Catalyzed by Rhodium
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol501619w
– volume: 9
  start-page: 4562
  year: 2018
  ident: WOS:000433426700003
  article-title: A chiral nickel DBFOX complex as a bifunctional catalyst for visible-light-promoted asymmetric photoredox reactions
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c8sc01219a
– volume: 57
  start-page: 4078
  year: 2018
  ident: WOS:000428350200039
  article-title: Selective C(sp(3))-H Aerobic Oxidation Enabled by Decatungstate Photocatalysis in Flow
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201800818
– volume: 57
  start-page: 259
  year: 2017
  ident: WOS:000398822700010
  article-title: Development of a Bio-Inspired Dual Catalytic System for Alkane Dehydrogenation
  publication-title: ISRAEL JOURNAL OF CHEMISTRY
  doi: 10.1002/ijch.201600115
– volume: 141
  start-page: 14394
  year: 2019
  ident: WOS:000486361800051
  article-title: Long-Lived, Strongly Emissive, and Highly Reducing Excited States in Mo(0) Complexes with Chelating Isocyanides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b07373
– volume: 140
  start-page: 13580
  year: 2018
  ident: WOS:000448755200013
  article-title: Cerium-Catalyzed Formal Cycloaddition of Cycloalkanols with Alkenes through Dual Photoexcitation
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b08781
– volume: 55
  start-page: 13244
  year: 2016
  ident: WOS:000385799200058
  article-title: A Convenient Late-Stage Fluorination of Pyridylic C-H Bonds with N-Fluorobenzenesulfonimide
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201606323
– volume: 360
  start-page: 932
  year: 2018
  ident: WOS:000426489300016
  article-title: Nondirecting Group sp(3) C-H Activation for Synthesis of Bibenzyls via Homo-coupling as Catalyzed by Reduced Graphene Oxide Supported PtPd@Pt Porous Nanospheres
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201701389
– volume: 4
  start-page: 359
  year: 2017
  ident: WOS:000406611700011
  article-title: Recent advances in visible-light-driven organic reactions
  publication-title: NATIONAL SCIENCE REVIEW
  doi: 10.1093/nsr/nwx039
– start-page: 1705
  year: 1984
  ident: WOS:A1984TN99400019
  article-title: TRIS(BIPYRIDYL)RUTHENIUM(II)-PHOTOSENSITIZED REACTION OF 1-BENZYL-1,4-DIHYDRONICOTINAMIDE WITH BENZYL BROMIDE
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2
– volume: 137
  start-page: 9234
  year: 2015
  ident: WOS:000358896600010
  article-title: Luminescent Ce(III) Complexes as Stoichiometric and Catalytic Photoreductants for Halogen Atom Abstraction Reactions
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.5b05411
– volume: 58
  start-page: 13318
  year: 2019
  ident: WOS:000479869100001
  article-title: Electrophotocatalysis with a Trisaminocyclopropenium Radical Dication
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201906381
– volume: 54
  start-page: 9985
  year: 2018
  ident: WOS:000443170200026
  article-title: Synthesis of acyl fluorides via photocatalytic fluorination of aldehydic C-H bonds
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc06375c
– volume: 40
  start-page: 9912
  year: 2016
  ident: WOS:000390724600006
  article-title: A well-defined low-valent cobalt catalyst Co(PMe3)(4) with dimethylzinc: a simple catalytic approach for the reductive dimerization of benzyl halides
  publication-title: NEW JOURNAL OF CHEMISTRY
  doi: 10.1039/c6nj03265f
– volume: 13
  start-page: 6264
  year: 2011
  ident: WOS:000297274700033
  article-title: Photoinduced Electron-Transfer-Promoted Redox Fragmentation of N-Alkoxyphthalimides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/ol202740w
– volume: 140
  start-page: 7667
  year: 2018
  ident: WOS:000436211600046
  article-title: C-N Cross-Coupling via Photoexcitation of Nickel-Amine Complexes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b03744
– volume: 142
  start-page: 2093
  year: 2020
  ident: WOS:000512222700002
  article-title: Potent Reductants via Electron-Primed Photoredox Catalysis: Unlocking Aryl Chlorides for Radical Coupling
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b12328
– volume: 124
  start-page: 6
  year: 2002
  ident: WOS:000173217900003
  article-title: Simple Cu(I) complexes with unprecedented excited-state lifetimes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja012247h
– volume: 49
  start-page: 1057
  year: 2020
  ident: WOS:000515511500008
  article-title: Photophysics and photochemistry with Earth-abundant metals - fundamentals and concepts
  publication-title: CHEMICAL SOCIETY REVIEWS
  doi: 10.1039/c9cs00573k
– volume: 3
  start-page: 875
  year: 2016
  ident: WOS:000382496400016
  article-title: Metal-free borylation of electron-rich aryl (pseudo)halides under continuous-flow photolytic conditions
  publication-title: ORGANIC CHEMISTRY FRONTIERS
  doi: 10.1039/c6qo00109b
– volume: 106
  start-page: 50
  year: 2018
  ident: WOS:000423640400011
  article-title: TBAI-catalyzed oxidative self-coupling of benzyl bromides under solvent-free conditions: A new pathway toward synthesis of benzyl benzoates
  publication-title: CATALYSIS COMMUNICATIONS
  doi: 10.1016/j.catcom.2017.12.012
– start-page: 3325
  year: 1992
  ident: WOS:A1992KC00900007
  article-title: PHOTOINDUCED C-C BOND FORMATION FROM ALKYL-HALIDES CATALYZED BY LUMINESCENT DINUCLEAR GOLD(I) AND COPPER(I) COMPLEXES
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS
– volume: 81
  start-page: 7155
  year: 2016
  ident: WOS:000381847600032
  article-title: Chemoselective Radical Dehalogenation and C-C Bond Formation on Aryl Halide Substrates Using Organic Photoredox Catalysts
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.6b01034
– volume: 53
  start-page: 2335
  year: 2017
  ident: WOS:000395874700007
  article-title: Versatile cross-dehydrogenative coupling of heteroaromatics and hydrogen donors via decatungstate photocatalysis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c6cc09725a
– volume: 57
  start-page: 9501
  year: 2018
  ident: WOS:000438712600051
  article-title: Cross-Coupling of Alkyl Redox-Active Esters with Benzophenone Imines: Tandem Photoredox and Copper Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201804873
– volume: 253
  start-page: 312
  year: 2008
  ident: WOS:000253282000011
  article-title: Selective photooxidation of diols with silica bound W10O324-
  publication-title: JOURNAL OF CATALYSIS
  doi: 10.1016/j.jcat.2007.11.008
– year: 2012
  ident: 000544484900023.18
  publication-title: Preparation of tungsten trioxide photocatalyst and its Application
– volume: 19
  start-page: 3576
  year: 2017
  ident: WOS:000405358300062
  article-title: A General Copper Catalyst for Photoredox Transformations of Organic Halides
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b01518
– volume: 363
  start-page: 249
  year: 2019
  ident: WOS:000456140700029
  article-title: Luminescence and reactivity of a charge-transfer excited iron complex with nanosecond lifetime
  publication-title: SCIENCE
  doi: 10.1126/science.aau7160
– volume: 62
  start-page: 1134
  year: 2004
  ident: WOS:000222218900008
  article-title: Study of preparation and photocatalytic activity of nanosized WO3 powder
  publication-title: ACTA CHIMICA SINICA
– start-page: 513
  year: 1983
  ident: WOS:A1983QN82300024
  article-title: BIS(2,9-DIPHENYL-1,10-PHENANTHROLINE)COPPER(I) - A COPPER COMPLEX WITH A LONG-LIVED CHARGE-TRANSFER EXCITED-STATE
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
– volume: 49
  start-page: 5891
  year: 2010
  ident: WOS:000281105600010
  article-title: Photochemical Addition of Ethers to C-60: Synthesis of the Simplest [60]Fullerene/Crown Ether Conjugates
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201002285
– volume: 139
  start-page: 607
  year: 2017
  ident: WOS:000392459300011
  article-title: Pyridine-Catalyzed Radical Borylation of Aryl Halides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b11813
– volume: 9
  start-page: 5708
  year: 2019
  ident: WOS:000471212600102
  article-title: Catalyst-Controlled C-H Functionalization of Adamantanes Using Selective H-Atom Transfer
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b01394
– volume: 560
  start-page: 70
  year: 2018
  ident: WOS:000440552600045
  article-title: Direct arylation of strong aliphatic C-H bonds
  publication-title: NATURE
  doi: 10.1038/s41586-018-0366-x
– volume: 5
  start-page: 5186
  year: 2015
  ident: WOS:000361089700026
  article-title: [Copper(phenanthroline)(bisisonitrile)(+)-Complexes for the Visible-Light-Mediated Atom Transfer Radical Addition and Allylation Reactions
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.5b01071
– volume: 51
  start-page: 784
  year: 2012
  ident: WOS:000299034200037
  article-title: Highly Efficient Aerobic Oxidative Hydroxylation of Arylboronic Acids: Photoredox Catalysis Using Visible Light
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201107028
– volume: 18
  start-page: 4743
  year: 2016
  ident: WOS:000382026600017
  article-title: Metal-free, visible-light-mediated, decarboxylative alkylation of biomass-derived compounds
  publication-title: GREEN CHEMISTRY
  doi: 10.1039/c6gc01101b
– volume: 81
  start-page: 6898
  year: 2016
  ident: WOS:000381847600002
  article-title: Photoredox Catalysis in Organic Chemistry
  publication-title: JOURNAL OF ORGANIC CHEMISTRY
  doi: 10.1021/acs.joc.6b01449
– volume: 142
  start-page: 2087
  year: 2020
  ident: WOS:000512222700001
  article-title: Reductive Electrophotocatalysis: Merging Electricity and Light To Achieve Extreme Reduction Potentials
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b10678
– volume: 136
  start-page: 3002
  year: 2014
  ident: WOS:000332144300018
  article-title: Photocatalytic Hydrodefluorination: Facile Access to Partially Fluorinated Aromatics
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja500031m
– volume: 57
  start-page: 14129
  year: 2018
  ident: WOS:000447371500024
  article-title: Air-Stable Blue Phosphorescent Tetradentate Platinum(II) Complexes as Strong Photo-Reductant
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201808642
– volume: 131
  start-page: 4063
  year: 2009
  ident: WOS:000264792700065
  article-title: Acyl Radical Reactions in Fullerene Chemistry: Direct Acylation of [60]Fullerene through an Efficient Decatungstate-Photomediated Approach
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/ja808658b
– volume: 51
  start-page: 12303
  year: 2012
  ident: WOS:000311706500030
  article-title: Visible-Light-Induced Photocatalytic Reductive Transformations of Organohalides
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201203599
– volume: 95
  start-page: 2457
  year: 1995
  ident: WOS:A1995TD89200007
  article-title: PALLADIUM-CATALYZED CROSS-COUPLING REACTIONS OF ORGANOBORON COMPOUNDS
  publication-title: CHEMICAL REVIEWS
– volume: 8
  start-page: 7489
  year: 2018
  ident: WOS:000441112400070
  article-title: Merging Photoredox and Copper Catalysis: Enantioselective Radical Cyanoalkylation of Styrenes
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.8b01863
– volume: 6
  start-page: 5426
  year: 2015
  ident: WOS:000361212000009
  article-title: Characterizing chain processes in visible light photoredox catalysis
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c5sc02185e
– volume: 55
  start-page: 15319
  year: 2016
  ident: WOS:000389224000023
  article-title: Photocatalytic C-C Bond Cleavage and Amination of Cycloalkanols by Cerium(III) Chloride Complex
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201609035
– volume: 55
  start-page: 11247
  year: 2016
  ident: WOS:000383642300053
  article-title: A Molybdenum(0) Isocyanide Analogue of Ru(2,2-Bipyridine)(3)(2+): A Strong Reductant for Photoredox Catalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201605571
– volume: 8
  start-page: 10809
  year: 2018
  ident: WOS:000449723900093
  article-title: Polyoxometalate Photocatalysis for Liquid-Phase Selective Organic Functional Group Transformations
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.8b03498
– volume: 54
  start-page: 10044
  year: 2018
  ident: WOS:000443956300046
  article-title: Application of coumarin dyes for organic photoredox catalysis
  publication-title: CHEMICAL COMMUNICATIONS
  doi: 10.1039/c8cc04048f
– volume: 138
  start-page: 8408
  year: 2016
  ident: WOS:000379794400023
  article-title: Additive- and Metal-Free, Predictably 1,2-and 1,3-Regioselective, Photoinduced Dual C-H/C-X Borylation of Haloarenes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b05436
– volume: 58
  start-page: 14896
  year: 2019
  ident: WOS:000490580800016
  article-title: Strongly Luminescent Tungsten Emitters with Emission Quantum Yields of up to 84 %: TADF and High-Efficiency Molecular Tungsten OLEDs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201906698
– volume: 20
  start-page: 349
  year: 2018
  ident: WOS:000423252400009
  article-title: Photoredox-Catalyzed Decarboxylative Alkylation of Silyl Enol Ethers To Synthesize Functionalized Aryl Alkyl Ketones
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.7b03587
– volume: 140
  start-page: 5934
  year: 2018
  ident: WOS:000432091700011
  article-title: A Zirconium Photosensitizer with a Long-Lived Excited State: Mechanistic Insight into Photoinduced Single-Electron Transfer
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b00742
– volume: 54
  start-page: 6506
  year: 2015
  ident: WOS:000355229800017
  article-title: Photooxidizing Chromium Catalysts for Promoting Radical Cation Cycloadditions
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201501220
– volume: 138
  start-page: 5984
  year: 2016
  ident: WOS:000375889100040
  article-title: Cerium Photosensitizers: Structure-Function Relationships and Applications in Photocatalytic Aryl Coupling Reactions
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b02248
– volume: 141
  start-page: 733
  year: 2019
  ident: WOS:000456350300003
  article-title: Lead-Halide Perovskites for Photocatalytic alpha-Alkylation of Aldehydes
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.8b08720
– volume: 233
  start-page: 351
  year: 2002
  ident: WOS:000178841400021
  article-title: Photosensitized singlet oxygen and its applications
  publication-title: COORDINATION CHEMISTRY REVIEWS
– volume: 1
  start-page: 111
  year: 2019
  ident: WOS:000521129500013
  article-title: Illuminating Photoredox Catalysis
  publication-title: TRENDS IN CHEMISTRY
  doi: 10.1016/j.trechm.2019.01.008
– volume: 127
  year: 1995
  ident: 000544484900023.41
  publication-title: Synlett
– volume: 25
  start-page: 3262
  year: 2019
  ident: WOS:000460679500015
  article-title: Copper-Photocatalyzed Borylation of Organic Halides under Batch and Continuous-Flow Conditions
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201806345
– volume: 94
  start-page: 722
  year: 1990
  ident: WOS:A1990CL43800039
  article-title: PHOTOCATALYTIC REDUCTION OF PHENACYL HALIDES BY 9,10-DIHYDRO-10-METHYLACRIDINE - CONTROL BETWEEN THE REDUCTIVE AND OXIDATIVE QUENCHING PATHWAYS OF TRIS(BIPYRIDINE)RUTHENIUM COMPLEX UTILIZING AN ACID CATALYSIS
  publication-title: JOURNAL OF PHYSICAL CHEMISTRY
– volume: 34
  start-page: 1397
  year: 1999
  ident: WOS:000083944500007
  article-title: Synthesis and luminescence of dioxo W6+ (d(0)) complex: BaWO2F4
  publication-title: MATERIALS RESEARCH BULLETIN
– volume: 56
  start-page: 14036
  year: 2017
  ident: WOS:000413896400020
  article-title: Highly Luminescent Pincer Gold(III) Aryl Emitters: Thermally Activated Delayed Fluorescence and Solution-Processed OLEDs
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201707193
– start-page: 546
  year: 1987
  ident: WOS:A1987H063800012
  article-title: PHOTOASSISTED C-C COUPLING VIA ELECTRON-TRANSFER TO BENZYLIC HALIDES BY A BIS(DI-IMINE) COPPER(1) COMPLEX
  publication-title: JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS
– volume: 54
  start-page: 8828
  year: 2015
  ident: WOS:000358051600048
  article-title: Photoredox-Catalyzed Reductive Coupling of Aldehydes, Ketones, and Imines with Visible Light
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201501556
– volume: 9
  start-page: 8276
  year: 2019
  ident: WOS:000485090400064
  article-title: Electrostatic Effects Accelerate Decatungstate-Catalyzed C-H Fluorination Using [F-18]- and [F-19]NFSI in Small Molecules and Peptide Mimics
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b02220
– volume: 53
  start-page: 4690
  year: 2014
  ident: WOS:000334894100034
  article-title: A Convenient Photocatalytic Fluorination of Unactivated C-H Bonds
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201400420
– volume: 10
  start-page: 11023
  year: 2019
  ident: WOS:000502319900004
  article-title: Reactivity control of a photocatalytic system by changing the light intensity
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c9sc04584h
– volume: 139
  start-page: 15632
  year: 2017
  ident: WOS:000415028200020
  article-title: Enantioselective Decarboxylative Cyanation Employing Cooperative Photoredox Catalysis and Copper Catalysis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.7b09802
– volume: 9
  start-page: 889
  year: 2019
  ident: WOS:000459893900001
  article-title: Photoredox catalysts based on earth-abundant metal complexes
  publication-title: CATALYSIS SCIENCE & TECHNOLOGY
  doi: 10.1039/c8cy02336k
– volume: 140
  start-page: 1612
  year: 2018
  ident: WOS:000424851500012
  article-title: delta-Selective Functionalization of Alkanols Enabled by Visible-Light-Induced Ligand-to-Metal Charge Transfer
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.7b13131
– volume: 24
  start-page: 2039
  year: 2018
  ident: WOS:000424792600002
  article-title: Photoredox Catalysis with Metal Complexes Made from Earth-Abundant Elements
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201703602
– volume: 46
  start-page: 13188
  year: 2017
  ident: WOS:000412765000006
  article-title: Two-photon spectroscopy of tungsten(0) arylisocyanides using nanosecond-pulsed excitation
  publication-title: DALTON TRANSACTIONS
  doi: 10.1039/c7dt02632c
– volume: 10
  start-page: 142
  year: 2004
  ident: WOS:000188087800014
  article-title: Polyoxotungstate photoinduced alkylation of electrophilic alkenes by cycloalkanes
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.200305285
– volume: 25
  start-page: 9991
  year: 2019
  ident: WOS:000476918500027
  article-title: Laser-Induced Wurtz-Type Syntheses with a Metal-Free Photoredox Catalytic Source of Hydrated Electrons
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201901618
– volume: 56
  start-page: 15274
  year: 2017
  ident: WOS:000416126600012
  article-title: Oxyfunctionalization of the Remote C-H Bonds of Aliphatic Amines by Decatungstate Photocatalysis
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201707537
– volume: 6
  start-page: ARTN 10093
  year: 2015
  ident: WOS:000367569500006
  article-title: Acceptorless dehydrogenation of small molecules through cooperative base metal catalysis
  publication-title: NATURE COMMUNICATIONS
  doi: 10.1038/ncomms10093
– volume: 113
  start-page: 9401
  year: 1991
  ident: WOS:A1991GQ93100074
  article-title: PHOTOSENSITIZED DECARBOXYLATIVE MICHAEL ADDITION THROUGH N-(ACYLOXY)PHTHALIMIDES VIA AN ELECTRON-TRANSFER MECHANISM
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 1
  start-page: 344
  year: 2017
  ident: WOS:000407646800001
  article-title: Photo-Chromium: Sensitizer for Visible-Light-Induced Oxidative C-H Bond FunctionalizationElectron or Energy Transfer?
  publication-title: CHEMPHOTOCHEM
  doi: 10.1002/cptc.201700077
– volume: 358
  start-page: 74
  year: 2016
  ident: WOS:000370256000011
  article-title: Selective Debromination and alpha-Hydroxylation of alpha-Bromo Ketones Using Hantzsch Esters as Photoreductants
  publication-title: ADVANCED SYNTHESIS & CATALYSIS
  doi: 10.1002/adsc.201500734
– volume: 10
  start-page: 6629
  year: 2019
  ident: WOS:000477947800003
  article-title: Enantioselective photoredox dehalogenative protonation
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c9sc02000d
– volume: 18
  start-page: 5248
  year: 2016
  ident: WOS:000386187300016
  article-title: Visible-Light Photoredox Borylation of Aryl Halides and Subsequent Aerobic Oxidative Hydroxylation
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.6b02553
– volume: 255
  start-page: 53
  year: 1997
  ident: WOS:A1997WK73100008
  article-title: Syntheses and luminescent properties of tetrahedral nickel(0) complexes
  publication-title: INORGANICA CHIMICA ACTA
– volume: 17
  start-page: 1292
  year: 2015
  ident: WOS:000350841300059
  article-title: Photocatalyzed Site-Selective C-H to C-C Conversion of Aliphatic Nitriles
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b00282
– volume: 138
  start-page: 16266
  year: 2016
  ident: WOS:000390729500020
  article-title: The Hexachlorocerate(III) Anion: A Potent, Benchtop Stable, and Readily Available Ultraviolet A Photosensitizer for Aryl Chlorides
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b05712
– volume: 23
  start-page: 8577
  year: 2017
  ident: WOS:000404147500004
  article-title: Luminescent Ni-0 Diisocyanide Chelates as Analogues of Cu-I Diimine Complexes
  publication-title: CHEMISTRY-A EUROPEAN JOURNAL
  doi: 10.1002/chem.201700103
– volume: 34
  start-page: 4640
  year: 1995
  ident: WOS:A1995RT11300021
  article-title: EARLY-TIME DYNAMICS AND REACTIVITY OF POLYOXOMETALATE EXCITED-STATES - IDENTIFICATION OF A SHORT-LIVED LMCT EXCITED-STATE AND A REACTIVE LONG-LIVED CHARGE-TRANSFER INTERMEDIATE FOLLOWING PICOSECOND FLASH EXCITATION OF [W10O32](4-) IN ACETONITRILE
  publication-title: INORGANIC CHEMISTRY
– volume: 3
  start-page: 143
  year: 2000
  ident: WOS:000085911600016
  article-title: Absorption and emission spectrum of bis-(triphenylphosphine)-dicarbonylnickel(0)
  publication-title: INORGANIC CHEMISTRY COMMUNICATIONS
– volume: 10
  start-page: 154
  year: 2020
  ident: WOS:000506725100018
  article-title: Bromide-Promoted Visible-Light-Induced Reductive Minisci Reaction with Aldehydes
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.9b04411
– volume: 17
  start-page: 5200
  year: 2015
  ident: WOS:000364434900014
  article-title: Development of a Direct Photocatalytic C-H Fluorination for the Preparative Synthesis of Odanacatib
  publication-title: ORGANIC LETTERS
  doi: 10.1021/acs.orglett.5b02532
– volume: 110
  start-page: 8736
  year: 1988
  ident: WOS:A1988R625200047
  article-title: A NEW AND PRACTICAL METHOD OF DECARBOXYLATION - PHOTOSENSITIZED DECARBOXYLATION OF N-ACYLOXYPHTHALIMIDES VIA ELECTRON-TRANSFER MECHANISM
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
– volume: 141
  start-page: 17646
  year: 2019
  ident: WOS:000495769300025
  article-title: The Tandem Photoredox Catalysis Mechanism of [Ir(ppy)(2)(dtb-bpy)](+) Enabling Access to Energy Demanding Organic Substrates
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.9b07370
– volume: 52
  start-page: 6648
  year: 2013
  ident: WOS:000320733600014
  article-title: Strongly Luminescent Gold(III) Complexes with Long-Lived Excited States: High Emission Quantum Yields, Energy Up-Conversion, and Nonlinear Optical Properties
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201301149
– volume: 5
  start-page: 5927
  year: 2015
  ident: WOS:000362391500028
  article-title: Organocatalytic Enantioselective Alkylation of Aldehydes with [Fe(bpy)(3)]Br-2 Catalyst and Visible Light
  publication-title: ACS CATALYSIS
  doi: 10.1021/acscatal.5b01573
– volume: 54
  start-page: 2084
  year: 2015
  ident: WOS:000349391000010
  article-title: Luminescent Pincer Platinum(II) Complexes with Emission Quantum Yields up to Almost Unity: Photophysics, Photoreductive C-C Bond Formation, and Materials Applications
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201408940
– volume: 11
  start-page: 488
  year: 2020
  ident: WOS:000505529100019
  article-title: Zn-mediated decarboxylative carbagermatranation of aliphatic N-hydroxyphthalimide esters: evidence for an alkylzinc intermediate
  publication-title: CHEMICAL SCIENCE
  doi: 10.1039/c9sc04288a
– volume: 1
  start-page: ARTN 0052
  year: 2017
  ident: WOS:000415236400002
  article-title: The merger of transition metal and photocatalysis
  publication-title: NATURE REVIEWS CHEMISTRY
  doi: 10.1038/s41570-017-0052
– volume: 359
  start-page: 52
  year: 2018
  ident: WOS:000424958800003
  article-title: Luminescent Ni(0) complexes
  publication-title: COORDINATION CHEMISTRY REVIEWS
  doi: 10.1016/j.ccr.2018.01.003
– volume: 138
  start-page: 5451
  year: 2016
  ident: WOS:000375244700043
  article-title: Uncovering the Roles of Oxygen in Cr(III) Photoredox Catalysis
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.6b02723
– volume: 52
  start-page: 718
  year: 2011
  ident: WOS:000287179900019
  article-title: Study on improved diastereoselectivity in photo-induced electron transfer pinacol coupling reactions of substituted acetophenones
  publication-title: TETRAHEDRON LETTERS
  doi: 10.1016/j.tetlet.2010.12.007
– volume: 140
  start-page: 3035
  year: 2018
  ident: WOS:000426617700049
  article-title: Long-Lived Charge-Transfer States of Nickel(II) Aryl Halide Complexes Facilitate Bimolecular Photoinduced Electron Transfer
  publication-title: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
  doi: 10.1021/jacs.7b13281
– volume: 52
  start-page: 13342
  year: 2013
  ident: WOS:000327802100039
  article-title: Photoredox Transformations with Dimeric Gold Complexes
  publication-title: ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
  doi: 10.1002/anie.201306727
SSID ssj0000331527
Score 2.47802
Snippet The realization of photocatalysis for practical synthetic application hinges on the development of inexpensive photocatalysts which can be prepared on a large...
A luminescent tungsten( vi ) complex catalyses a broad spectrum of light-driven organic transformation reactions with high product yields and good functional...
Source Web of Science
SourceID pubmedcentral
proquest
pubmed
webofscience
crossref
rsc
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage 637
SubjectTerms Aromatic compounds
Bonding
Bromides
Carboxylic acids
Chemistry
Chemistry, Multidisciplinary
Coupling
Covalent bonds
Electromagnetic absorption
Esters
Functional groups
Halides
NMR
Nuclear magnetic resonance
Photocatalysis
Photocatalysts
Photochemical reactions
Photoluminescence
Physical Sciences
Science & Technology
Tungsten
Title Luminescent tungsten() complexes as photocatalysts for light-driven C-C and C-B bond formation reactions
URI http://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcApp=Summon&SrcAuth=ProQuest&DestApp=WOS&DestLinkType=FullRecord&UT=000544484900023
https://www.ncbi.nlm.nih.gov/pubmed/32874518
https://www.proquest.com/docview/2419016969
https://www.proquest.com/docview/2439633176
https://pubmed.ncbi.nlm.nih.gov/PMC7448528
Volume 11
WOS 000544484900023
WOSCitedRecordID wos000544484900023
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV3NbtQwELbarQS9IP4KKaUyogeqKCVrJ05ypClQIYoq2kJ7iuLYYVdqk1U3WwEn3oE34xF4EsZO4mTVPZReoqwzSjaeL-OZ8fgzQltC5MTLeeqwUASOl3nS4STkDs-4x2SWejxXeciDT2z_xPtw6p8uLf3pVS3NKr6T_Vy4ruQ2WoU20KtaJfsfmjU3hQY4B_3CETQMxxvp-OPsQlWtqwJLu4KvFjSmKjuuxirW18Xi8rucqq1kJqOyKnWq5se00hQM9rmmEBGXytzZcVv0QOtizu73rs3VEhezyNEGLzPrsnwtyUHLO9AuE1KTw-1ysF624WxWF9KXo7IZMnWGW1f6pWPncK61NkPvYVwsUvuotA_G3dWvszqjkBbfHH3spy8gVtWpUQO4OknSVqjqCpRmn7vOEBLXGzrMJ_X8jey31URIxpIPe4glfs8uMxq4vTEejA5ZOH64VNGvCneagWvsuaIvBLqfXGgkUb1JQDNuzLN1Hx7EAUS8PgmX0QqB0IUM0MrnLyenZybz51La7CVsXqzlzaXR6-7Zq-hO-6B5p-laJHS9oHf5cpotdKW023R8H91r4h38pgbvA7Qki4forun-R6jogRi3IH51Nd7GBsA4neJ5AGOAI-4DGMd_f_2OMUBXn-1iBVpsQIsNaB-jk3dvj-N9p9kExMmgYyonysOQsVSwMBQkzakirAOfOhQRH0Y5ZUxIJria3fZ57nI3C0OaS8lTX8LgIghdQ4OiLORThP0s4OATKgpICGSCNA0EIS7NfbhzJn1moe22l5OsYchXG7WcJ7pSg0bJnnsUa-XsWeilkZ3UvDALpTZaZSWN3Zgm4DNHigOJRRZ6YS5Dr6upurSQ5UzJUBgZwbeHP_Wk1q15TAsKCwVzWjcCijF-_koxHmnm-AaaFloDfBj5DnIWWl98IZmI3EJbfTwZKR32wY29SLNnWWh4E7G46WBFvVGt3_pVnqHVzqpsoEF1OZPPIUyo-KZOr202X98_S8gWkQ
linkProvider Royal Society of Chemistry
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Luminescent+tungsten%28vi%29+complexes+as+photocatalysts+for+light-driven+C%E2%80%93C+and+C%E2%80%93B+bond+formation+reactions&rft.jtitle=Chemical+science+%28Cambridge%29&rft.au=Yu%2C+Daohong&rft.au=To%2C+Wai-Pong&rft.au=Tong%2C+Glenna+So+Ming&rft.au=Wu%2C+Liang-Liang&rft.date=2020-07-07&rft.pub=Royal+Society+of+Chemistry&rft.issn=2041-6520&rft.eissn=2041-6539&rft.volume=11&rft.issue=25&rft.spage=6370&rft.epage=6382&rft_id=info:doi/10.1039%2Fd0sc01340d&rft_id=info%3Apmid%2F32874518&rft.externalDocID=PMC7448528
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=2041-6520&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=2041-6520&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=2041-6520&client=summon