N-heterocyclic silylenes as powerful steering ligands in catalysis

The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in...

Full description

Saved in:
Bibliographic Details
Published inJournal of organometallic chemistry Vol. 829; pp. 2 - 10
Main Authors Raoufmoghaddam, Saeed, Zhou, Yu-Peng, Wang, Yuwen, Driess, Matthias
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.02.2017
Subjects
Online AccessGet full text

Cover

Loading…
Abstract The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in organic synthesis. Despite significant advances in the synthesis of NHSi-based metal complexes, the use of these compounds in organic methodologies is still in its initial stages. Since NHSi ligands promote the σ donor-ability of phosphines and even that of NHCs, they can facilitate catalytic events by lowering the energy barrier of the rate limiting steps such as oxidative additions. This encourages scientists to utilize NHSi-metal complexes in exploiting catalyzed reactions and to revisit and improve various existing organic methodologies. This is demonstrated in several showcases of organic transformations including the Heck coupling, Suzuki coupling, alkyne and ketone hydrosilylation, amide reduction, cyclotrimerization of alkynes (in the absence and the presence of an organo cyanide), and Sonogashira cross-coupling reactions. The latter represents a novel and unexpected steering function of NHSi-based systems in homogeneous catalysis. [Display omitted] •Synthesis and catalytic performance of monodentate, bidentate, and tridentate NHSi-transition metal complexes.•Stronger σ donor strength of NHSi ligands in comparison to NHCs and phosphines.•Catalytic performances of transition metal NHSi complexes.
AbstractList The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various catalytic organic transformations. The application of such novel ligands coordinated by different metal sites offers massive opportunities in organic synthesis. Despite significant advances in the synthesis of NHSi-based metal complexes, the use of these compounds in organic methodologies is still in its initial stages. Since NHSi ligands promote the σ donor-ability of phosphines and even that of NHCs, they can facilitate catalytic events by lowering the energy barrier of the rate limiting steps such as oxidative additions. This encourages scientists to utilize NHSi-metal complexes in exploiting catalyzed reactions and to revisit and improve various existing organic methodologies. This is demonstrated in several showcases of organic transformations including the Heck coupling, Suzuki coupling, alkyne and ketone hydrosilylation, amide reduction, cyclotrimerization of alkynes (in the absence and the presence of an organo cyanide), and Sonogashira cross-coupling reactions. The latter represents a novel and unexpected steering function of NHSi-based systems in homogeneous catalysis. [Display omitted] •Synthesis and catalytic performance of monodentate, bidentate, and tridentate NHSi-transition metal complexes.•Stronger σ donor strength of NHSi ligands in comparison to NHCs and phosphines.•Catalytic performances of transition metal NHSi complexes.
Author Raoufmoghaddam, Saeed
Zhou, Yu-Peng
Wang, Yuwen
Driess, Matthias
Author_xml – sequence: 1
  givenname: Saeed
  surname: Raoufmoghaddam
  fullname: Raoufmoghaddam, Saeed
– sequence: 2
  givenname: Yu-Peng
  surname: Zhou
  fullname: Zhou, Yu-Peng
– sequence: 3
  givenname: Yuwen
  surname: Wang
  fullname: Wang, Yuwen
– sequence: 4
  givenname: Matthias
  surname: Driess
  fullname: Driess, Matthias
  email: matthias.driess@tu-berlin.de
BookMark eNqNkM1KAzEUhYNUsFbfIS8wY346k3Qj2OIfFN0ouAtJ5k6bIc2UJCrz9k6pILjR1YEL57uc7xxNQh8AIUxJSQmtr7qy6-NGB7uFXcnGS0lESej8BE2pFKyQVU0naEoIYwVn8u0MnafUEUIoJ3KKlk_FFjLE3g7WO4uT84OHAAnrhPf9J8T23eOUAaILG-zd-KpJ2AVsddZ-SC5doNNW-wSX3zlDr3e3L6uHYv18_7i6WReWU5kLY7jg7ULOK8OaBafcSmlgXjFKoBWG6lpSJpihi1ZbUzHWCGiYgJoTUzdU8Bm6PnJt7FOK0Crrss6uDzlq5xUl6mBEderHiDoYUUSo0cgIkL8A--h2Og7_qS6PVRgHfjiIKlkHwULjItismt79DfkCf2WFNw
CitedBy_id crossref_primary_10_1002_chem_201700829
crossref_primary_10_1002_anie_202108146
crossref_primary_10_1021_acs_inorgchem_4c01695
crossref_primary_10_1080_00268976_2023_2211906
crossref_primary_10_1002_ange_201609520
crossref_primary_10_1016_j_tet_2018_12_063
crossref_primary_10_1039_D0SC02861D
crossref_primary_10_1016_j_comptc_2023_114020
crossref_primary_10_1039_C9DT01853K
crossref_primary_10_1039_D4DT03537B
crossref_primary_10_1002_anie_201606979
crossref_primary_10_1002_chem_201700828
crossref_primary_10_1016_S1872_2067_17_62994_2
crossref_primary_10_1021_acs_inorgchem_0c00843
crossref_primary_10_1002_ejic_202000479
crossref_primary_10_1016_j_polymer_2019_121748
crossref_primary_10_1021_jacs_7b07167
crossref_primary_10_1002_ange_202208202
crossref_primary_10_1002_poc_4148
crossref_primary_10_1002_anie_202110456
crossref_primary_10_1039_D1DT00523E
crossref_primary_10_1002_anie_202208202
crossref_primary_10_1016_j_ccr_2022_214837
crossref_primary_10_1021_acs_organomet_0c00188
crossref_primary_10_1002_ange_202410792
crossref_primary_10_1002_ejic_202000360
crossref_primary_10_1039_D0DT00659A
crossref_primary_10_1021_acs_organomet_2c00480
crossref_primary_10_1021_acs_inorgchem_8b00321
crossref_primary_10_1002_ange_202011598
crossref_primary_10_1002_chem_202001062
crossref_primary_10_1039_D1DT00617G
crossref_primary_10_1002_chem_201605937
crossref_primary_10_1021_jacs_7b08667
crossref_primary_10_1039_C9DT00608G
crossref_primary_10_1039_C9CC03128F
crossref_primary_10_1002_aoc_6286
crossref_primary_10_1021_acs_organomet_0c00195
crossref_primary_10_1021_acs_organomet_1c00526
crossref_primary_10_1021_acs_organomet_1c00083
crossref_primary_10_1016_j_molstruc_2021_132192
crossref_primary_10_1021_acs_organomet_2c00293
crossref_primary_10_1039_C7DT03301J
crossref_primary_10_1021_acs_accounts_2c00763
crossref_primary_10_3390_M1433
crossref_primary_10_1021_acs_inorgchem_3c02445
crossref_primary_10_1002_anie_202011598
crossref_primary_10_1055_s_0041_1741035
crossref_primary_10_1002_jccs_202000113
crossref_primary_10_1002_asia_202401058
crossref_primary_10_1016_j_ccr_2022_214942
crossref_primary_10_3390_inorganics6030069
crossref_primary_10_1002_chem_201802625
crossref_primary_10_5059_yukigoseikyokaishi_76_1301
crossref_primary_10_1002_ejic_202200175
crossref_primary_10_1021_acs_organomet_1c00238
crossref_primary_10_1016_j_jorganchem_2018_02_047
crossref_primary_10_1039_D3SC06452B
crossref_primary_10_1002_ejic_202000942
crossref_primary_10_1021_acs_inorgchem_2c01233
crossref_primary_10_1021_acs_chemrev_8b00079
crossref_primary_10_1021_jacs_1c05510
crossref_primary_10_1002_chem_202000235
crossref_primary_10_1002_chem_201805406
crossref_primary_10_1002_zaac_202200084
crossref_primary_10_1039_C7DT04155A
crossref_primary_10_1039_D1CC01939B
crossref_primary_10_1039_D3CS00226H
crossref_primary_10_1007_s12633_020_00745_2
crossref_primary_10_1021_acs_organomet_8b00700
crossref_primary_10_1002_chem_202403368
crossref_primary_10_1039_C8CC03734E
crossref_primary_10_1002_anie_201609520
crossref_primary_10_1039_D1CC04100B
crossref_primary_10_1039_C7CC08690C
crossref_primary_10_1039_D1NJ02982G
crossref_primary_10_1002_ange_201606979
crossref_primary_10_1002_chem_201705745
crossref_primary_10_1021_acs_organomet_0c00025
crossref_primary_10_1002_chem_202000866
crossref_primary_10_1016_j_jorganchem_2021_122133
crossref_primary_10_3390_inorganics11080318
crossref_primary_10_1039_D0OB01351J
crossref_primary_10_1021_acs_organomet_2c00040
crossref_primary_10_1002_ejic_202300209
crossref_primary_10_1039_D1DT01955D
crossref_primary_10_1021_acs_organomet_8b00399
crossref_primary_10_1021_jacs_9b06603
crossref_primary_10_1002_anie_202013622
crossref_primary_10_1021_jacs_8b11605
crossref_primary_10_1039_C7CC04832G
crossref_primary_10_1002_anie_202016455
crossref_primary_10_1039_C8DT00121A
crossref_primary_10_1021_acs_inorgchem_3c04135
crossref_primary_10_1002_ange_201705153
crossref_primary_10_1002_anie_202402795
crossref_primary_10_1002_ange_202108146
crossref_primary_10_1021_acs_organomet_1c00203
crossref_primary_10_1002_ange_201811088
crossref_primary_10_1002_ejic_202100446
crossref_primary_10_1021_acs_inorgchem_0c00426
crossref_primary_10_1039_D4CC01930J
crossref_primary_10_1039_D1DT01754C
crossref_primary_10_1002_ange_202013622
crossref_primary_10_1002_anie_202410792
crossref_primary_10_1002_ejic_202000737
crossref_primary_10_1039_D3DT03843B
crossref_primary_10_3390_molecules25245917
crossref_primary_10_1021_acs_organomet_8b00171
crossref_primary_10_1007_s12633_021_00998_5
crossref_primary_10_1021_jacs_1c06654
crossref_primary_10_1002_ange_202016455
crossref_primary_10_1002_ange_202402795
crossref_primary_10_1021_jacs_2c10467
crossref_primary_10_1002_anie_201811088
crossref_primary_10_1002_ange_202110456
crossref_primary_10_1002_chem_201803089
crossref_primary_10_1021_acs_inorgchem_0c01462
crossref_primary_10_1021_jacs_7b13536
crossref_primary_10_1002_anie_201705153
Cites_doi 10.1002/anie.200804993
10.1021/cr1003503
10.1002/anie.201200632
10.1039/c3cs60146c
10.1039/C4RA14417A
10.1021/ja910305p
10.1021/cr5002782
10.1021/ja062928i
10.1246/cl.2013.286
10.1016/j.ccr.2015.04.008
10.1021/ja106458p
10.1002/ange.19770891116
10.1002/zaac.200800131
10.1021/ja402480v
10.1002/anie.201106131
10.1039/C5SC02855H
10.1002/anie.197707851
10.1002/anie.201409739
10.1021/om050010e
10.1039/c1cs15071e
10.1002/anie.201205570
10.1021/ja9091374
10.1021/om500966t
10.1002/anie.200703883
10.1039/c1cs15088j
10.1039/c2cs35102a
10.1021/ja00070a047
10.1002/anie.201202175
10.1021/ar700028b
10.1021/ja408137t
10.1002/chem.201203072
10.1039/C3QI00079F
10.1039/b108132b
10.1039/b711132k
10.1071/CH13196
10.1021/cr050992x
10.1021/cr900074m
10.1038/nature13384
ContentType Journal Article
Copyright 2016 Elsevier B.V.
Copyright_xml – notice: 2016 Elsevier B.V.
DBID AAYXX
CITATION
DOI 10.1016/j.jorganchem.2016.07.014
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1872-8561
EndPage 10
ExternalDocumentID 10_1016_j_jorganchem_2016_07_014
S0022328X16302984
GroupedDBID --K
--M
-~X
.~1
0R~
1B1
1RT
1~.
1~5
4.4
457
4G.
5GY
5VS
7-5
71M
8P~
9JM
9JN
AABNK
AABXZ
AACTN
AAEDT
AAEDW
AAEPC
AAIAV
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AARLI
AAXUO
ABFRF
ABGSF
ABJNI
ABMAC
ABUDA
ABXRA
ABYKQ
ACBEA
ACDAQ
ACGFO
ACGFS
ACNCT
ACRLP
ADBBV
ADECG
ADEZE
ADUVX
AEBSH
AEFWE
AEHWI
AEKER
AENEX
AEZYN
AFKWA
AFRZQ
AFTJW
AFXIZ
AFZHZ
AGHFR
AGUBO
AGYEJ
AHHHB
AIEXJ
AIKHN
AITUG
AJBFU
AJOXV
AJSZI
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
AXJTR
BKOJK
BLXMC
CS3
DOVZS
EBS
EFJIC
EFLBG
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FIRID
FLBIZ
FNPLU
FYGXN
G-Q
GBLVA
IHE
J1W
K-O
KOM
M23
M41
MAGPM
MO0
N9A
O-L
O9-
OAUVE
OZT
P-8
P-9
P2P
PC.
Q38
RIG
RNS
ROL
RPZ
SCC
SDF
SDG
SDP
SES
SPC
SPCBC
SSK
SSM
SSU
SSZ
T5K
TN5
TWZ
WH7
XPP
YK3
YQT
ZMT
~G-
29L
3EH
6TJ
AAQXK
AATTM
AAXKI
AAYWO
AAYXX
ABEFU
ABFNM
ABWVN
ABXDB
ACNNM
ACRPL
ACVFH
ADCNI
ADIYS
ADMUD
ADNMO
AEIPS
AEUPX
AFJKZ
AFPUW
AGCQF
AGQPQ
AGRDE
AGRNS
AI.
AIGII
AIIUN
AKBMS
AKRWK
AKYEP
ANKPU
APXCP
ASPBG
AVWKF
AZFZN
BBWZM
BNPGV
CITATION
FEDTE
FGOYB
HMH
HVGLF
HZ~
H~9
NDZJH
OHT
R2-
SCB
SEW
SIC
SSH
UQL
VH1
WUQ
XJT
ZCG
ID FETCH-LOGICAL-c318t-bb373f9845b2d9313c88be45210ef7b1a681272b19facb522d7ed27e630b6d173
IEDL.DBID .~1
ISSN 0022-328X
IngestDate Tue Jul 01 01:17:41 EDT 2025
Thu Apr 24 22:52:36 EDT 2025
Fri Feb 23 02:30:22 EST 2024
IsPeerReviewed true
IsScholarly true
Keywords Silylenes
Hydrosilylation
Pincer ligands
Silicon analogues of carbenes
Homogeneous catalysis
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c318t-bb373f9845b2d9313c88be45210ef7b1a681272b19facb522d7ed27e630b6d173
PageCount 9
ParticipantIDs crossref_citationtrail_10_1016_j_jorganchem_2016_07_014
crossref_primary_10_1016_j_jorganchem_2016_07_014
elsevier_sciencedirect_doi_10_1016_j_jorganchem_2016_07_014
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2017-02-01
2017-02-00
PublicationDateYYYYMMDD 2017-02-01
PublicationDate_xml – month: 02
  year: 2017
  text: 2017-02-01
  day: 01
PublicationDecade 2010
PublicationTitle Journal of organometallic chemistry
PublicationYear 2017
Publisher Elsevier B.V
Publisher_xml – name: Elsevier B.V
References Sen, Roesky, Stern, Henn, Stalke (bib23) 2010; 132
Neumann, Pfaltz (bib21) 2005; 24
Fortman, Nolan (bib2) 2011; 40
Hopkinson, Richter, Schedler, Glorius (bib1) 2014; 510
Someya, Haberberger, Wang, Enthaler, Inoue (bib12) 2013; 42
Blom, Gallego, Driess (bib11) 2014; 1
Driess, Yao, Brym, van Wuellen, Lentz (bib22) 2006; 128
Zhang, Liu, Shi, Ren, Ding, Roesky (bib26) 2008; 634
Wang, Inoue, Irran, Driess (bib33) 2012; 51
Hahn, Jahnke (bib3) 2008; 47
Meltzer, Inoue, Praesang, Driess (bib24) 2010; 132
Blom, Stoelzel, Driess (bib19) 2013; 19
Chinchilla, Najera (bib37) 2011; 40
Blom, Enthaler, Inoue, Irran, Driess (bib27) 2013; 135
Wang, Inoue, Yao, Driess (bib29) 2010; 132
Tan, Enthaler, Inoue, Blom, Driess (bib9) 2015; 54
Diez-Gonzalez, Marion, Nolan (bib5) 2009; 109
Metsänen, Gallego, Szilvási, Driess, Oestreich (bib10) 2015; 6
Benedek, Szilvasi (bib25) 2015; 5
Gallego, Inoue, Blom, Driess (bib38) 2014; 33
Nelson, Nolan (bib4) 2013; 42
Valente, Calimsiz, Hoi, Mallik, Sayah, Organ (bib7) 2012; 51
Wang, Inoue, Enthaler, Driess (bib30) 2012; 51
Schneider, Finger, Haferkemper, Bellemin-Laponnaz, Hofmann, Gade (bib13) 2009; 48
Waterman, Hayes, Tilley (bib14) 2007; 40
Stoelzel, Praesang, Blom, Driess (bib28) 2013; 66
Alvarez-Rodriguez, Cabeza, Garcia-Alvarez, Polo (bib16) 2015; 300
Schmid, Welz (bib17) 1977; 16
Brueck, Gallego, Wang, Irran, Driess, Hartwig (bib34) 2012; 51
Marion, Nolan (bib6) 2008; 37
Velazquez, Verpoort (bib8) 2012; 41
Chinchilla, Najera (bib36) 2007; 107
Grumbine, Tilley, Arnold, Rheingold (bib20) 1993; 115
Gunanathan, Milstein (bib31) 2014; 114
Furstner, Krause, Lehmann (bib18) 2001
Choi, MacArthur, Brookhart, Goldman (bib32) 2011; 111
Gallego, Brueck, Irran, Meier, Kaupp, Driess, Hartwig (bib35) 2013; 135
Schmid, Welz (bib15) 1977; 89
Sen (10.1016/j.jorganchem.2016.07.014_bib23) 2010; 132
Wang (10.1016/j.jorganchem.2016.07.014_bib30) 2012; 51
Schmid (10.1016/j.jorganchem.2016.07.014_bib15) 1977; 89
Hahn (10.1016/j.jorganchem.2016.07.014_bib3) 2008; 47
Zhang (10.1016/j.jorganchem.2016.07.014_bib26) 2008; 634
Marion (10.1016/j.jorganchem.2016.07.014_bib6) 2008; 37
Chinchilla (10.1016/j.jorganchem.2016.07.014_bib37) 2011; 40
Wang (10.1016/j.jorganchem.2016.07.014_bib33) 2012; 51
Velazquez (10.1016/j.jorganchem.2016.07.014_bib8) 2012; 41
Tan (10.1016/j.jorganchem.2016.07.014_bib9) 2015; 54
Valente (10.1016/j.jorganchem.2016.07.014_bib7) 2012; 51
Choi (10.1016/j.jorganchem.2016.07.014_bib32) 2011; 111
Driess (10.1016/j.jorganchem.2016.07.014_bib22) 2006; 128
Meltzer (10.1016/j.jorganchem.2016.07.014_bib24) 2010; 132
Wang (10.1016/j.jorganchem.2016.07.014_bib29) 2010; 132
Furstner (10.1016/j.jorganchem.2016.07.014_bib18) 2001
Chinchilla (10.1016/j.jorganchem.2016.07.014_bib36) 2007; 107
Brueck (10.1016/j.jorganchem.2016.07.014_bib34) 2012; 51
Benedek (10.1016/j.jorganchem.2016.07.014_bib25) 2015; 5
Alvarez-Rodriguez (10.1016/j.jorganchem.2016.07.014_bib16) 2015; 300
Metsänen (10.1016/j.jorganchem.2016.07.014_bib10) 2015; 6
Waterman (10.1016/j.jorganchem.2016.07.014_bib14) 2007; 40
Gallego (10.1016/j.jorganchem.2016.07.014_bib38) 2014; 33
Nelson (10.1016/j.jorganchem.2016.07.014_bib4) 2013; 42
Schmid (10.1016/j.jorganchem.2016.07.014_bib17) 1977; 16
Blom (10.1016/j.jorganchem.2016.07.014_bib19) 2013; 19
Diez-Gonzalez (10.1016/j.jorganchem.2016.07.014_bib5) 2009; 109
Someya (10.1016/j.jorganchem.2016.07.014_bib12) 2013; 42
Grumbine (10.1016/j.jorganchem.2016.07.014_bib20) 1993; 115
Fortman (10.1016/j.jorganchem.2016.07.014_bib2) 2011; 40
Stoelzel (10.1016/j.jorganchem.2016.07.014_bib28) 2013; 66
Gallego (10.1016/j.jorganchem.2016.07.014_bib35) 2013; 135
Blom (10.1016/j.jorganchem.2016.07.014_bib27) 2013; 135
Hopkinson (10.1016/j.jorganchem.2016.07.014_bib1) 2014; 510
Blom (10.1016/j.jorganchem.2016.07.014_bib11) 2014; 1
Schneider (10.1016/j.jorganchem.2016.07.014_bib13) 2009; 48
Neumann (10.1016/j.jorganchem.2016.07.014_bib21) 2005; 24
Gunanathan (10.1016/j.jorganchem.2016.07.014_bib31) 2014; 114
References_xml – volume: 89
  start-page: 823
  year: 1977
  end-page: 824
  ident: bib15
  publication-title: Angew. Chem.
– volume: 40
  start-page: 5151
  year: 2011
  end-page: 5169
  ident: bib2
  publication-title: Chem. Soc. Rev.
– volume: 132
  start-page: 15890
  year: 2010
  end-page: 15892
  ident: bib29
  publication-title: J. Am. Chem. Soc.
– volume: 24
  start-page: 2008
  year: 2005
  end-page: 2011
  ident: bib21
  publication-title: Organometallics
– volume: 107
  start-page: 874
  year: 2007
  end-page: 922
  ident: bib36
  publication-title: Chem. Rev.
– volume: 47
  start-page: 3122
  year: 2008
  end-page: 3172
  ident: bib3
  publication-title: Angew. Chem. Int. Ed.
– volume: 111
  start-page: 1761
  year: 2011
  end-page: 1779
  ident: bib32
  publication-title: Chem. Rev.
– volume: 33
  start-page: 6885
  year: 2014
  end-page: 6897
  ident: bib38
  publication-title: Organometallics
– volume: 510
  start-page: 485
  year: 2014
  end-page: 496
  ident: bib1
  publication-title: Nature
– volume: 115
  start-page: 7884
  year: 1993
  end-page: 7885
  ident: bib20
  publication-title: J. Am. Chem. Soc.
– volume: 5
  start-page: 5077
  year: 2015
  end-page: 5086
  ident: bib25
  publication-title: Rsc Adv.
– volume: 300
  start-page: 1
  year: 2015
  end-page: 28
  ident: bib16
  publication-title: Coord. Chem. Rev.
– volume: 128
  start-page: 9628
  year: 2006
  end-page: 9629
  ident: bib22
  publication-title: J. Am. Chem. Soc.
– volume: 51
  start-page: 6167
  year: 2012
  end-page: 6171
  ident: bib30
  publication-title: Angew. Chem. Int. Ed.
– volume: 634
  start-page: 1755
  year: 2008
  end-page: 1758
  ident: bib26
  publication-title: Z. Anorg. Allg. Chem.
– volume: 114
  start-page: 12024
  year: 2014
  end-page: 12087
  ident: bib31
  publication-title: Chem. Rev.
– volume: 16
  start-page: 785
  year: 1977
  end-page: 786
  ident: bib17
  publication-title: Angew. Chem. Int. Ed. Engl.
– volume: 37
  start-page: 1776
  year: 2008
  end-page: 1782
  ident: bib6
  publication-title: Chem. Soc. Rev.
– volume: 54
  start-page: 2214
  year: 2015
  end-page: 2218
  ident: bib9
  publication-title: Angew. Chem. Int. Ed.
– volume: 66
  start-page: 1163
  year: 2013
  end-page: 1170
  ident: bib28
  publication-title: Aust. J. Chem.
– volume: 51
  start-page: 3691
  year: 2012
  end-page: 3694
  ident: bib33
  publication-title: Angew. Chem. Int. Ed.
– volume: 40
  start-page: 5084
  year: 2011
  end-page: 5121
  ident: bib37
  publication-title: Chem. Soc. Rev.
– volume: 41
  start-page: 7032
  year: 2012
  end-page: 7060
  ident: bib8
  publication-title: Chem. Soc. Rev.
– volume: 40
  start-page: 712
  year: 2007
  end-page: 719
  ident: bib14
  publication-title: Acc. Chem. Res.
– volume: 132
  start-page: 1123
  year: 2010
  end-page: 1126
  ident: bib23
  publication-title: J. Am. Chem. Soc.
– volume: 51
  start-page: 3314
  year: 2012
  end-page: 3332
  ident: bib7
  publication-title: Angew. Chem. Int. Ed.
– volume: 42
  start-page: 286
  year: 2013
  end-page: 288
  ident: bib12
  publication-title: Chem. Lett.
– volume: 135
  start-page: 6703
  year: 2013
  end-page: 6713
  ident: bib27
  publication-title: J. Am. Chem. Soc.
– volume: 132
  start-page: 3038
  year: 2010
  end-page: 3046
  ident: bib24
  publication-title: J. Am. Chem. Soc.
– volume: 19
  start-page: 40
  year: 2013
  end-page: 62
  ident: bib19
  publication-title: Chem. Eur. J.
– volume: 48
  start-page: 1609
  year: 2009
  end-page: 1613
  ident: bib13
  publication-title: Angew. Chem. Int. Ed.
– start-page: 2372
  year: 2001
  end-page: 2373
  ident: bib18
  publication-title: Chem. Commun.
– volume: 135
  start-page: 15617
  year: 2013
  end-page: 15626
  ident: bib35
  publication-title: J. Am. Chem. Soc.
– volume: 42
  start-page: 6723
  year: 2013
  end-page: 6753
  ident: bib4
  publication-title: Chem. Soc. Rev.
– volume: 1
  start-page: 134
  year: 2014
  end-page: 148
  ident: bib11
  publication-title: Inorg. Chem. Front.
– volume: 51
  start-page: 11478
  year: 2012
  end-page: 11482
  ident: bib34
  publication-title: Angew. Chem. Int. Ed.
– volume: 109
  start-page: 3612
  year: 2009
  end-page: 3676
  ident: bib5
  publication-title: Chem. Rev.
– volume: 6
  start-page: 7143
  year: 2015
  end-page: 7149
  ident: bib10
  publication-title: Chem. Sci.
– volume: 48
  start-page: 1609
  year: 2009
  ident: 10.1016/j.jorganchem.2016.07.014_bib13
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200804993
– volume: 111
  start-page: 1761
  year: 2011
  ident: 10.1016/j.jorganchem.2016.07.014_bib32
  publication-title: Chem. Rev.
  doi: 10.1021/cr1003503
– volume: 51
  start-page: 3691
  year: 2012
  ident: 10.1016/j.jorganchem.2016.07.014_bib33
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201200632
– volume: 42
  start-page: 6723
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib4
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c3cs60146c
– volume: 5
  start-page: 5077
  year: 2015
  ident: 10.1016/j.jorganchem.2016.07.014_bib25
  publication-title: Rsc Adv.
  doi: 10.1039/C4RA14417A
– volume: 132
  start-page: 3038
  year: 2010
  ident: 10.1016/j.jorganchem.2016.07.014_bib24
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja910305p
– volume: 114
  start-page: 12024
  year: 2014
  ident: 10.1016/j.jorganchem.2016.07.014_bib31
  publication-title: Chem. Rev.
  doi: 10.1021/cr5002782
– volume: 128
  start-page: 9628
  year: 2006
  ident: 10.1016/j.jorganchem.2016.07.014_bib22
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja062928i
– volume: 42
  start-page: 286
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib12
  publication-title: Chem. Lett.
  doi: 10.1246/cl.2013.286
– volume: 300
  start-page: 1
  year: 2015
  ident: 10.1016/j.jorganchem.2016.07.014_bib16
  publication-title: Coord. Chem. Rev.
  doi: 10.1016/j.ccr.2015.04.008
– volume: 132
  start-page: 15890
  year: 2010
  ident: 10.1016/j.jorganchem.2016.07.014_bib29
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja106458p
– volume: 89
  start-page: 823
  year: 1977
  ident: 10.1016/j.jorganchem.2016.07.014_bib15
  publication-title: Angew. Chem.
  doi: 10.1002/ange.19770891116
– volume: 634
  start-page: 1755
  year: 2008
  ident: 10.1016/j.jorganchem.2016.07.014_bib26
  publication-title: Z. Anorg. Allg. Chem.
  doi: 10.1002/zaac.200800131
– volume: 135
  start-page: 6703
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib27
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja402480v
– volume: 51
  start-page: 3314
  year: 2012
  ident: 10.1016/j.jorganchem.2016.07.014_bib7
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201106131
– volume: 6
  start-page: 7143
  year: 2015
  ident: 10.1016/j.jorganchem.2016.07.014_bib10
  publication-title: Chem. Sci.
  doi: 10.1039/C5SC02855H
– volume: 16
  start-page: 785
  year: 1977
  ident: 10.1016/j.jorganchem.2016.07.014_bib17
  publication-title: Angew. Chem. Int. Ed. Engl.
  doi: 10.1002/anie.197707851
– volume: 54
  start-page: 2214
  year: 2015
  ident: 10.1016/j.jorganchem.2016.07.014_bib9
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201409739
– volume: 24
  start-page: 2008
  year: 2005
  ident: 10.1016/j.jorganchem.2016.07.014_bib21
  publication-title: Organometallics
  doi: 10.1021/om050010e
– volume: 40
  start-page: 5084
  year: 2011
  ident: 10.1016/j.jorganchem.2016.07.014_bib37
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15071e
– volume: 51
  start-page: 11478
  year: 2012
  ident: 10.1016/j.jorganchem.2016.07.014_bib34
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201205570
– volume: 132
  start-page: 1123
  year: 2010
  ident: 10.1016/j.jorganchem.2016.07.014_bib23
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja9091374
– volume: 33
  start-page: 6885
  year: 2014
  ident: 10.1016/j.jorganchem.2016.07.014_bib38
  publication-title: Organometallics
  doi: 10.1021/om500966t
– volume: 47
  start-page: 3122
  year: 2008
  ident: 10.1016/j.jorganchem.2016.07.014_bib3
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.200703883
– volume: 40
  start-page: 5151
  year: 2011
  ident: 10.1016/j.jorganchem.2016.07.014_bib2
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c1cs15088j
– volume: 41
  start-page: 7032
  year: 2012
  ident: 10.1016/j.jorganchem.2016.07.014_bib8
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/c2cs35102a
– volume: 115
  start-page: 7884
  year: 1993
  ident: 10.1016/j.jorganchem.2016.07.014_bib20
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja00070a047
– volume: 51
  start-page: 6167
  year: 2012
  ident: 10.1016/j.jorganchem.2016.07.014_bib30
  publication-title: Angew. Chem. Int. Ed.
  doi: 10.1002/anie.201202175
– volume: 40
  start-page: 712
  year: 2007
  ident: 10.1016/j.jorganchem.2016.07.014_bib14
  publication-title: Acc. Chem. Res.
  doi: 10.1021/ar700028b
– volume: 135
  start-page: 15617
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib35
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/ja408137t
– volume: 19
  start-page: 40
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib19
  publication-title: Chem. Eur. J.
  doi: 10.1002/chem.201203072
– volume: 1
  start-page: 134
  year: 2014
  ident: 10.1016/j.jorganchem.2016.07.014_bib11
  publication-title: Inorg. Chem. Front.
  doi: 10.1039/C3QI00079F
– start-page: 2372
  year: 2001
  ident: 10.1016/j.jorganchem.2016.07.014_bib18
  publication-title: Chem. Commun.
  doi: 10.1039/b108132b
– volume: 37
  start-page: 1776
  year: 2008
  ident: 10.1016/j.jorganchem.2016.07.014_bib6
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/b711132k
– volume: 66
  start-page: 1163
  year: 2013
  ident: 10.1016/j.jorganchem.2016.07.014_bib28
  publication-title: Aust. J. Chem.
  doi: 10.1071/CH13196
– volume: 107
  start-page: 874
  year: 2007
  ident: 10.1016/j.jorganchem.2016.07.014_bib36
  publication-title: Chem. Rev.
  doi: 10.1021/cr050992x
– volume: 109
  start-page: 3612
  year: 2009
  ident: 10.1016/j.jorganchem.2016.07.014_bib5
  publication-title: Chem. Rev.
  doi: 10.1021/cr900074m
– volume: 510
  start-page: 485
  year: 2014
  ident: 10.1016/j.jorganchem.2016.07.014_bib1
  publication-title: Nature
  doi: 10.1038/nature13384
SSID ssj0001308
Score 2.5156953
SecondaryResourceType review_article
Snippet The present review highlights the role of N-heterocyclic silylene (NHSi) ligands, the silicon analogues of N-heterocyclic carbenes (NHCs), utilized in various...
SourceID crossref
elsevier
SourceType Enrichment Source
Index Database
Publisher
StartPage 2
SubjectTerms Homogeneous catalysis
Hydrosilylation
Pincer ligands
Silicon analogues of carbenes
Silylenes
Title N-heterocyclic silylenes as powerful steering ligands in catalysis
URI https://dx.doi.org/10.1016/j.jorganchem.2016.07.014
Volume 829
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV1NS8NAEF1KPehF_MT6UfbgdW2y2WY3eKrFUhV7stDbsrvZaEpIi20Pvfjbnc1HqyAoeA0ZSF5m5w3hzRuErqnHlLCBJUaYiDDKNBFRl5HYeCruUguM6AaFn0fhcMweJ91JA_XrWRgnq6xqf1nTi2pdXelUaHbmaepmfIHaqJhAR-F8xJ0nKGPcZfnNx1bmATVabBzD4e5KzVNqvKbF6iRAx82k-6WNp89-pqgvtDM4QPtVv4h75SMdoobNj9Buv17TdozuRuTNSVpmZm2y1OBFmq0zV8CwWuC524GWrDIM37LwHMRZ-uqGe3Ga4-LPjTMkOUHjwf1Lf0iqxQjEwBFcEq0DHiTwyl1N4yjwAyOEtgyY2LMJ175ypmKcaj9KlNHQYcXcxpRbAEqHsc-DU9TMZ7k9Q9iKMKKhCplQnAkNxzdS1ksUDaMkCQLeQrzGQprKNdwtr8hkLQ-byi2K0qEoPS4BxRbyN5Hz0jnjDzG3NdzyWxZIKPC_Rp__K_oC7VFH2YUi-xI1l-8rewUNx1K3i4xqo53ew9Nw9AlRvtcT
linkProvider Elsevier
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV09T8MwELVKGcqC-BTl0wNraOK4sSMmqEAF2k6t1M2yHQdSRWlF26ELv51zPlqQkEBijXJS8uK7d4revUPomrhUcuMbR3MdOpRQ5fCwTZ1IuzJqEwOMaAeF-4OgO6LP4_a4hjrVLIyVVZa1v6jpebUur7RKNFuzJLEzvkBthI-ho7A-4nQLbVNIX7vG4OZjo_OAIs3XluFweynnKURek3x3EsBjh9K9wsfToz9z1BfeedxDu2XDiO-KZ9pHNZMdoEan2tN2iO4HzpvVtEz1SqeJxvMkXaW2gmE5xzO7BC1ephg-Zm46iNPk1U734iTD-a8b60hyhEaPD8NO1yk3IzgacnDhKOUzP4Z3bisShb7na86VoUDFromZ8qR1FWNEeWEstYIWK2ImIswAUiqIPOYfo3o2zcwJwoYHIQlkQLlklCvI31AaN5YkCOPY91kTsQoLoUvbcLu9IhWVPmwiNigKi6JwmQAUm8hbR84K64w_xNxWcItvx0BAhf81-vRf0Veo0R32e6L3NHg5QzvE8ncuzz5H9cX70lxA97FQl_np-gRfptih
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=N-heterocyclic+silylenes+as+powerful+steering+ligands+in+catalysis&rft.jtitle=Journal+of+organometallic+chemistry&rft.au=Raoufmoghaddam%2C+Saeed&rft.au=Zhou%2C+Yu-Peng&rft.au=Wang%2C+Yuwen&rft.au=Driess%2C+Matthias&rft.date=2017-02-01&rft.pub=Elsevier+B.V&rft.issn=0022-328X&rft.eissn=1872-8561&rft.volume=829&rft.spage=2&rft.epage=10&rft_id=info:doi/10.1016%2Fj.jorganchem.2016.07.014&rft.externalDocID=S0022328X16302984
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0022-328X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0022-328X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0022-328X&client=summon