High‐Fidelity, Narcissistic Self‐Sorting in the Synthesis of Organometallic Assemblies from Poly‐NHC Ligands
Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type [M3{L‐(NHC)3}2](PF6)3 (M=Ag+, Au+; L=1,3,5‐benzene, triphenylamine, or 1,3,5‐triphenylbenzene) from L‐(NHC)3 and silver(I) or gold(I) ions. The molecular cylinde...
Saved in:
Published in | Angewandte Chemie International Edition Vol. 56; no. 26; pp. 7393 - 7397 |
---|---|
Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
19.06.2017
|
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Abstract | Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type [M3{L‐(NHC)3}2](PF6)3 (M=Ag+, Au+; L=1,3,5‐benzene, triphenylamine, or 1,3,5‐triphenylbenzene) from L‐(NHC)3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris‐NHC ligand with no crossover products detectable. Transmetalation of the tris‐NHC ligands from Ag+ to Au+ in a one‐pot reaction with retention of the supramolecular structures is also demonstrated. High‐fidelity self‐sorting was also observed in the one‐pot reaction of benzene‐bridged tris‐NHC and tetrakis‐NHC ligands with Ag2O. This study for the first time extends narcissistic self‐sorting in metal–ligand interactions from Werner‐type complexes to organometallic derivatives.
Perfect sorting! Unique narcissistic self‐sorting has been observed in the one‐pot reaction of three different trigonal trisimidazolium salts with Ag2O. Only three cylinder‐like trinuclear complexes each bearing two identical tris‐NHC ligands were obtained from this reaction. Self‐sorting was also observed in the subsequent transmetalation of the tris‐NHC ligands from the three silver(I) complexes to give three gold(I) complexes. |
---|---|
AbstractList | Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M3{L-(NHC)3}2](PF6)3 (M=Ag+, Au+; L=1,3,5-benzene, triphenylamine, or 1,3,5-triphenylbenzene) from L-(NHC)3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris-NHC ligand with no crossover products detectable. Transmetalation of the tris-NHC ligands from Ag+ to Au+ in a one-pot reaction with retention of the supramolecular structures is also demonstrated. High-fidelity self-sorting was also observed in the one-pot reaction of benzene-bridged tris-NHC and tetrakis-NHC ligands with Ag2O. This study for the first time extends narcissistic self-sorting in metal-ligand interactions from Werner-type complexes to organometallic derivatives. Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M3 {L-(NHC)3 }2 ](PF6 )3 (M=Ag+ , Au+ ; L=1,3,5-benzene, triphenylamine, or 1,3,5-triphenylbenzene) from L-(NHC)3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris-NHC ligand with no crossover products detectable. Transmetalation of the tris-NHC ligands from Ag+ to Au+ in a one-pot reaction with retention of the supramolecular structures is also demonstrated. High-fidelity self-sorting was also observed in the one-pot reaction of benzene-bridged tris-NHC and tetrakis-NHC ligands with Ag2 O. This study for the first time extends narcissistic self-sorting in metal-ligand interactions from Werner-type complexes to organometallic derivatives.Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M3 {L-(NHC)3 }2 ](PF6 )3 (M=Ag+ , Au+ ; L=1,3,5-benzene, triphenylamine, or 1,3,5-triphenylbenzene) from L-(NHC)3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris-NHC ligand with no crossover products detectable. Transmetalation of the tris-NHC ligands from Ag+ to Au+ in a one-pot reaction with retention of the supramolecular structures is also demonstrated. High-fidelity self-sorting was also observed in the one-pot reaction of benzene-bridged tris-NHC and tetrakis-NHC ligands with Ag2 O. This study for the first time extends narcissistic self-sorting in metal-ligand interactions from Werner-type complexes to organometallic derivatives. Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M {L-(NHC) } ](PF ) (M=Ag , Au ; L=1,3,5-benzene, triphenylamine, or 1,3,5-triphenylbenzene) from L-(NHC) and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris-NHC ligand with no crossover products detectable. Transmetalation of the tris-NHC ligands from Ag to Au in a one-pot reaction with retention of the supramolecular structures is also demonstrated. High-fidelity self-sorting was also observed in the one-pot reaction of benzene-bridged tris-NHC and tetrakis-NHC ligands with Ag O. This study for the first time extends narcissistic self-sorting in metal-ligand interactions from Werner-type complexes to organometallic derivatives. Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type [M3{L‐(NHC)3}2](PF6)3 (M=Ag+, Au+; L=1,3,5‐benzene, triphenylamine, or 1,3,5‐triphenylbenzene) from L‐(NHC)3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris‐NHC ligand with no crossover products detectable. Transmetalation of the tris‐NHC ligands from Ag+ to Au+ in a one‐pot reaction with retention of the supramolecular structures is also demonstrated. High‐fidelity self‐sorting was also observed in the one‐pot reaction of benzene‐bridged tris‐NHC and tetrakis‐NHC ligands with Ag2O. This study for the first time extends narcissistic self‐sorting in metal–ligand interactions from Werner‐type complexes to organometallic derivatives. Perfect sorting! Unique narcissistic self‐sorting has been observed in the one‐pot reaction of three different trigonal trisimidazolium salts with Ag2O. Only three cylinder‐like trinuclear complexes each bearing two identical tris‐NHC ligands were obtained from this reaction. Self‐sorting was also observed in the subsequent transmetalation of the tris‐NHC ligands from the three silver(I) complexes to give three gold(I) complexes. Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type [M 3 {L‐(NHC) 3 } 2 ](PF 6 ) 3 (M=Ag + , Au + ; L=1,3,5‐benzene, triphenylamine, or 1,3,5‐triphenylbenzene) from L‐(NHC) 3 and silver(I) or gold(I) ions. The molecular cylinders contain only one type of tris‐NHC ligand with no crossover products detectable. Transmetalation of the tris‐NHC ligands from Ag + to Au + in a one‐pot reaction with retention of the supramolecular structures is also demonstrated. High‐fidelity self‐sorting was also observed in the one‐pot reaction of benzene‐bridged tris‐NHC and tetrakis‐NHC ligands with Ag 2 O. This study for the first time extends narcissistic self‐sorting in metal–ligand interactions from Werner‐type complexes to organometallic derivatives. |
Author | Tan, Tristan T. Y. Peris, Eduardo Hahn, F. Ekkehardt Sinha, Narayan |
Author_xml | – sequence: 1 givenname: Narayan surname: Sinha fullname: Sinha, Narayan organization: Westfälische Wilhelms-Universität Münster – sequence: 2 givenname: Tristan T. Y. surname: Tan fullname: Tan, Tristan T. Y. organization: Westfälische Wilhelms-Universität Münster – sequence: 3 givenname: Eduardo surname: Peris fullname: Peris, Eduardo organization: Universitat Jaume I – sequence: 4 givenname: F. Ekkehardt orcidid: 0000-0002-2807-7232 surname: Hahn fullname: Hahn, F. Ekkehardt email: fehahn@uni-muenster.de organization: Westfälische Wilhelms-Universität Münster |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28544306$$D View this record in MEDLINE/PubMed |
BookMark | eNqFkU1rGzEQhkVJaT7aa49F0EsPXVff0h6NSeqAcQpuz4t2d9ZR0EqptCb41p_Q39hfUhmnKQRKTyOY55kZ9J6jkxADIPSWkhklhH2ywcGMEaoJU1y_QGdUMlpxrflJeQvOK20kPUXnOd8V3hiiXqFTZqQQnKgzlJZue_vrx88r14N30_4jXtvUuZxdnlyHN-CH0t3ENLmwxS7g6RbwZh9KKQiOA75JWxviCJP1vhjznGFsvYOMhxRH_CX6fZmwXi7wyhWyz6_Ry8H6DG8e6wX6dnX5dbGsVjefrxfzVdUJrXRlLRuskL3UrTXKGmEFSKZZbxmo2vBWStCyVYrX1tRCkMEMShEGtO47ATW_QB-Oc-9T_L6DPDWjyx14bwPEXW5oTTgttuYFff8MvYu7FMp1B0ozLmtqCvXukdq1I_TNfXKjTfvmz28WYHYEuhRzTjA8IZQ0h7iaQ1zNU1xFEM-Ezk12cjFMyTr_b60-ag_Ow_4_S5r5-vryr_sbPkSsIQ |
CitedBy_id | crossref_primary_10_1021_acs_chemrev_8b00119 crossref_primary_10_1515_znb_2021_0087 crossref_primary_10_1002_chem_201803948 crossref_primary_10_3762_bjoc_16_233 crossref_primary_10_1021_jacs_0c06470 crossref_primary_10_1021_acs_accounts_3c00102 crossref_primary_10_1038_s41467_024_50972_z crossref_primary_10_1002_cplu_202000153 crossref_primary_10_1021_acsami_8b05073 crossref_primary_10_1002_ijch_201800173 crossref_primary_10_1039_C8CC05707A crossref_primary_10_1016_j_jcat_2020_06_004 crossref_primary_10_1002_asia_202000603 crossref_primary_10_1002_ange_201810010 crossref_primary_10_1002_adom_202202516 crossref_primary_10_1039_D2CC04561C crossref_primary_10_1021_acs_inorgchem_8b00498 crossref_primary_10_1039_D2CC04496J crossref_primary_10_1039_D4DT02953D crossref_primary_10_1039_C7SC04927G crossref_primary_10_1002_ange_202206788 crossref_primary_10_1007_s11426_023_1919_2 crossref_primary_10_1021_acs_accounts_7b00158 crossref_primary_10_1016_j_jssc_2020_121561 crossref_primary_10_1021_jacs_7b09025 crossref_primary_10_1002_chem_201704540 crossref_primary_10_1002_chem_201806204 crossref_primary_10_1002_adom_202300534 crossref_primary_10_1002_aoc_6517 crossref_primary_10_1002_anie_201810010 crossref_primary_10_1016_j_ica_2018_03_027 crossref_primary_10_1007_s11426_021_1041_8 crossref_primary_10_1039_C9CC02341K crossref_primary_10_1021_acs_organomet_8b00874 crossref_primary_10_1002_ange_202202190 crossref_primary_10_1002_anie_201912322 crossref_primary_10_1021_acs_inorgchem_8b00668 crossref_primary_10_1039_C8DT00169C crossref_primary_10_1002_chem_202303101 crossref_primary_10_1002_ejic_202200216 crossref_primary_10_1007_s11426_020_9937_4 crossref_primary_10_1039_C8NJ01503A crossref_primary_10_1016_j_cclet_2022_01_064 crossref_primary_10_1002_anie_202206788 crossref_primary_10_1002_anie_202202190 crossref_primary_10_1002_cjoc_202300026 crossref_primary_10_1002_adom_202401793 crossref_primary_10_1002_ejic_201900097 crossref_primary_10_1039_C7NJ04020B crossref_primary_10_1002_cplu_202000739 crossref_primary_10_1002_ange_201912322 crossref_primary_10_1002_chem_201901880 crossref_primary_10_1016_j_matchemphys_2022_126316 crossref_primary_10_1039_D1SC06413D crossref_primary_10_1002_chem_202000122 crossref_primary_10_1039_D1CC01652K crossref_primary_10_1039_C9PY00848A crossref_primary_10_1039_D4CC01239A crossref_primary_10_1515_znb_2024_0090 crossref_primary_10_1021_acs_organomet_1c00119 crossref_primary_10_14233_ajomc_2021_AJOMC_P331 crossref_primary_10_1002_chem_201703868 |
Cites_doi | 10.1002/1521-3757(20021104)114:21<4200::AID-ANGE4200>3.0.CO;2-L 10.1021/ja101490d 10.1038/171737a0 10.1039/C5CC05114B 10.1002/ange.201107227 10.1002/anie.200703883 10.1002/(SICI)1521-3773(19980420)37:7<932::AID-ANIE932>3.0.CO;2-C 10.1126/science.1188605 10.1021/jo049976a 10.1002/(SICI)1521-3757(19980403)110:7<977::AID-ANGE977>3.0.CO;2-D 10.1002/ange.201000165 10.1039/C0CC04476H 10.1021/ja310083p 10.1021/jacs.5b09920 10.1002/chem.200900230 10.1002/ange.19971091309 10.1002/anie.199714401 10.1002/(SICI)1521-3773(19990215)38:4<557::AID-ANIE557>3.0.CO;2-S 10.1021/ja028913b 10.1002/(SICI)1521-3757(19990215)111:4<512::AID-ANGE512>3.0.CO;2-Y 10.1021/om500973b 10.1002/anie.201408652 10.1021/om500729b 10.1038/nchem.693 10.1002/ange.201502983 10.1039/c3cs60098j 10.1021/ja803847w 10.1021/cr100357h 10.1073/pnas.90.12.5394 10.1021/cr8005153 10.1002/ange.201408652 10.1039/b902238b 10.1021/om101102j 10.1002/1521-3773(20021104)41:21<4028::AID-ANIE4028>3.0.CO;2-2 10.1021/ja0202006 10.1039/C3DT53243G 10.1021/ja992821d 10.1002/anie.201502983 10.1002/ange.200703883 10.1021/ja027489b 10.1073/pnas.0809903106 10.1021/ja4032067 10.1002/anie.201000165 10.1002/anie.201107227 10.1039/C4CS00305E 10.1039/C2CS35123D |
ContentType | Journal Article |
Copyright | 2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim |
Copyright_xml | – notice: 2017 Wiley‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. – notice: 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim |
DBID | AAYXX CITATION NPM 7TM K9. 7X8 |
DOI | 10.1002/anie.201702637 |
DatabaseName | CrossRef PubMed Nucleic Acids Abstracts ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic |
DatabaseTitle | CrossRef PubMed ProQuest Health & Medical Complete (Alumni) Nucleic Acids Abstracts MEDLINE - Academic |
DatabaseTitleList | ProQuest Health & Medical Complete (Alumni) MEDLINE - Academic PubMed 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 |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
EISSN | 1521-3773 |
Edition | International ed. in English |
EndPage | 7397 |
ExternalDocumentID | 28544306 10_1002_anie_201702637 ANIE201702637 |
Genre | shortCommunication Research Support, Non-U.S. Gov't Journal Article |
GrantInformation_xml | – fundername: DFG funderid: IRTG 2027 and SFB 858 |
GroupedDBID | --- -DZ -~X .3N .GA 05W 0R~ 10A 1L6 1OB 1OC 1ZS 23M 33P 3SF 3WU 4.4 4ZD 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5RE 5VS 66C 6TJ 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 930 A03 AAESR AAEVG AAHHS AAHQN AAMNL AANLZ AAONW AASGY AAXRX AAYCA AAZKR ABCQN ABCUV ABEML ABIJN ABLJU ABPPZ ABPVW ACAHQ ACCFJ ACCZN ACFBH ACGFS ACIWK ACNCT ACPOU ACPRK ACSCC ACXBN ACXQS ADBBV ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AEQDE AEUQT AEUYR AFBPY AFFNX AFFPM AFGKR AFPWT AFRAH AFWVQ AFZJQ AHBTC AHMBA AITYG AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN ALVPJ AMBMR AMYDB ATUGU AUFTA AZBYB AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BTSUX BY8 CS3 D-E D-F D0L DCZOG DPXWK DR1 DR2 DRFUL DRSTM EBS EJD F00 F01 F04 F5P G-S G.N GNP GODZA H.T H.X HBH HGLYW HHY HHZ HZ~ IX1 J0M JPC KQQ LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LW6 LYRES M53 MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ NNB O66 O9- OIG P2P P2W P2X P4D PQQKQ Q.N Q11 QB0 QRW R.K RNS ROL RWI RX1 RYL SUPJJ TN5 UB1 UPT V2E VQA W8V W99 WBFHL WBKPD WH7 WIB WIH WIK WJL WOHZO WQJ WRC WXSBR WYISQ XG1 XPP XSW XV2 YZZ ZZTAW ~IA ~KM ~WT AAYXX ABDBF ABJNI AETEA AEYWJ AGHNM AGYGG CITATION NPM YIN 7TM K9. 7X8 |
ID | FETCH-LOGICAL-c4767-aa2fa45d57ba86a84a4e5272da2e6983b55e75b6639a89440f8f6602e19dc4e93 |
IEDL.DBID | DR2 |
ISSN | 1433-7851 1521-3773 |
IngestDate | Fri Jul 11 07:22:31 EDT 2025 Sun Jul 13 04:37:56 EDT 2025 Wed Feb 19 02:33:27 EST 2025 Tue Jul 01 02:26:03 EDT 2025 Thu Apr 24 23:01:44 EDT 2025 Wed Jan 22 16:45:51 EST 2025 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 26 |
Keywords | organometallic complexes silver and gold narcissistic self-sorting supramolecular chemistry poly-NHC ligands |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c4767-aa2fa45d57ba86a84a4e5272da2e6983b55e75b6639a89440f8f6602e19dc4e93 |
Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ORCID | 0000-0002-2807-7232 |
PMID | 28544306 |
PQID | 1907235918 |
PQPubID | 946352 |
PageCount | 5 |
ParticipantIDs | proquest_miscellaneous_1903163973 proquest_journals_1907235918 pubmed_primary_28544306 crossref_primary_10_1002_anie_201702637 crossref_citationtrail_10_1002_anie_201702637 wiley_primary_10_1002_anie_201702637_ANIE201702637 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | June 19, 2017 |
PublicationDateYYYYMMDD | 2017-06-19 |
PublicationDate_xml | – month: 06 year: 2017 text: June 19, 2017 day: 19 |
PublicationDecade | 2010 |
PublicationPlace | Germany |
PublicationPlace_xml | – name: Germany – name: Weinheim |
PublicationTitle | Angewandte Chemie International Edition |
PublicationTitleAlternate | Angew Chem Int Ed Engl |
PublicationYear | 2017 |
Publisher | Wiley Subscription Services, Inc |
Publisher_xml | – name: Wiley Subscription Services, Inc |
References | 2014 2014; 53 126 2010; 328 2015; 51 2010; 39 2004; 69 1999 1999; 38 111 2013; 42 1999; 121 2011; 30 2010 2010; 49 122 1993; 90 2008 2008; 47 120 1953; 171 2011; 111 2014; 43 1998 1998; 37 110 2002 2002; 41 114 2015; 137 2002; 124 2012 2012; 51 124 2015; 44 2010; 132 2015 2015; 54 127 2013; 135 1997 1997; 36 109 2011; 47 2003; 125 2010; 2 2009; 109 2008; 130 2009; 15 2014; 33 2009; 106 e_1_2_2_24_2 e_1_2_2_4_2 e_1_2_2_22_2 e_1_2_2_6_2 e_1_2_2_20_2 e_1_2_2_2_1 e_1_2_2_41_2 e_1_2_2_28_3 e_1_2_2_8_2 e_1_2_2_28_2 e_1_2_2_43_2 e_1_2_2_45_1 e_1_2_2_26_2 e_1_2_2_8_3 e_1_2_2_13_2 e_1_2_2_38_2 e_1_2_2_11_1 e_1_2_2_19_3 e_1_2_2_19_2 e_1_2_2_30_2 e_1_2_2_17_3 e_1_2_2_17_2 e_1_2_2_32_2 e_1_2_2_32_3 e_1_2_2_34_2 e_1_2_2_15_1 e_1_2_2_34_3 e_1_2_2_36_1 e_1_2_2_23_2 e_1_2_2_5_2 e_1_2_2_7_1 e_1_2_2_21_2 e_1_2_2_1_1 e_1_2_2_3_1 e_1_2_2_40_2 e_1_2_2_42_1 e_1_2_2_29_2 e_1_2_2_27_2 e_1_2_2_44_2 e_1_2_2_44_3 e_1_2_2_9_2 e_1_2_2_25_2 e_1_2_2_12_3 e_1_2_2_12_2 e_1_2_2_37_2 e_1_2_2_39_2 e_1_2_2_10_1 e_1_2_2_18_3 e_1_2_2_31_1 e_1_2_2_18_2 e_1_2_2_16_2 e_1_2_2_33_2 e_1_2_2_35_1 e_1_2_2_14_2 |
References_xml | – volume: 111 start-page: 5784 year: 2011 end-page: 5814 publication-title: Chem. Rev. – volume: 125 start-page: 667 year: 2003 end-page: 671 publication-title: J. Am. Chem. Soc. – volume: 137 start-page: 14502 year: 2015 end-page: 14512 publication-title: J. Am. Chem. Soc. – volume: 121 start-page: 11538 year: 1999 end-page: 11545 publication-title: J. Am. Chem. Soc. – volume: 39 start-page: 1903 year: 2010 end-page: 1912 publication-title: Chem. Soc. Rev. – volume: 33 start-page: 6898 year: 2014 end-page: 6904 publication-title: Organometallics – volume: 49 122 start-page: 8810 8992 year: 2010 2010 end-page: 8849 9032 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 38 111 start-page: 557 512 year: 1999 1999 end-page: 559 515 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 42 start-page: 1619 year: 2013 end-page: 1636 publication-title: Chem. Soc. Rev. – volume: 106 start-page: 10430 year: 2009 end-page: 10434 publication-title: Proc. Natl. Acad. Sci. USA – volume: 90 start-page: 5394 year: 1993 end-page: 5398 publication-title: Proc. Natl. Acad. Sci. USA – volume: 2 start-page: 684 year: 2010 end-page: 687 publication-title: Nat. Chem. – volume: 15 start-page: 7203 year: 2009 end-page: 7214 publication-title: Chem. Eur. J. – volume: 41 114 start-page: 4028 4200 year: 2002 2002 end-page: 4031 4203 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 37 110 start-page: 932 977 year: 1998 1998 end-page: 935 981 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 135 start-page: 9263 year: 2013 end-page: 9266 publication-title: J. Am. Chem. Soc. – volume: 44 start-page: 779 year: 2015 end-page: 789 publication-title: Chem. Soc. Rev. – volume: 33 start-page: 5077 year: 2014 end-page: 5080 publication-title: Organometallics – volume: 132 start-page: 4572 year: 2010 end-page: 4573 publication-title: J. Am. Chem. Soc. – volume: 125 start-page: 4831 year: 2003 end-page: 4835 publication-title: J. Am. Chem. Soc. – volume: 109 start-page: 3561 year: 2009 end-page: 3598 publication-title: Chem. Rev. – volume: 47 120 start-page: 3122 3166 year: 2008 2008 end-page: 3172 3216 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 69 start-page: 6157 year: 2004 end-page: 6164 publication-title: J. Org. Chem. – volume: 47 start-page: 1830 year: 2011 end-page: 1832 publication-title: Chem. Commun. – volume: 42 start-page: 6860 year: 2013 end-page: 6909 publication-title: Chem. Soc. Rev. – volume: 135 start-page: 554 year: 2013 end-page: 557 publication-title: J. Am. Chem. Soc. – volume: 51 start-page: 13914 year: 2015 end-page: 13917 publication-title: Chem. Commun. – volume: 53 126 start-page: 13510 13728 year: 2014 2014 end-page: 13513 13731 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 54 127 start-page: 10356 10497 year: 2015 2015 end-page: 10360 10502 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 328 start-page: 1144 year: 2010 end-page: 1147 publication-title: Science – volume: 51 124 start-page: 2195 2238 year: 2012 2012 end-page: 2198 2241 publication-title: Angew. Chem. Int. Ed. Angew. Chem. – volume: 130 start-page: 11641 year: 2008 end-page: 11649 publication-title: J. Am. Chem. Soc. – volume: 36 109 start-page: 1440 1508 year: 1997 1997 end-page: 1442 1510 publication-title: Angew. Chem. Int. Ed. Engl. Angew. Chem. – volume: 30 start-page: 334 year: 2011 end-page: 347 publication-title: Organometallics – volume: 171 start-page: 737 year: 1953 end-page: 738 publication-title: Nature – volume: 124 start-page: 13757 year: 2002 end-page: 13769 publication-title: J. Am. Chem. Soc. – volume: 43 start-page: 4587 year: 2014 end-page: 4592 publication-title: Dalton Trans. – ident: e_1_2_2_12_3 doi: 10.1002/1521-3757(20021104)114:21<4200::AID-ANGE4200>3.0.CO;2-L – ident: e_1_2_2_41_2 doi: 10.1021/ja101490d – ident: e_1_2_2_2_1 doi: 10.1038/171737a0 – ident: e_1_2_2_37_2 doi: 10.1039/C5CC05114B – ident: e_1_2_2_44_3 doi: 10.1002/ange.201107227 – ident: e_1_2_2_34_2 doi: 10.1002/anie.200703883 – ident: e_1_2_2_31_1 – ident: e_1_2_2_18_2 doi: 10.1002/(SICI)1521-3773(19980420)37:7<932::AID-ANIE932>3.0.CO;2-C – ident: e_1_2_2_23_2 doi: 10.1126/science.1188605 – ident: e_1_2_2_45_1 – ident: e_1_2_2_15_1 – ident: e_1_2_2_5_2 doi: 10.1021/jo049976a – ident: e_1_2_2_18_3 doi: 10.1002/(SICI)1521-3757(19980403)110:7<977::AID-ANGE977>3.0.CO;2-D – ident: e_1_2_2_32_3 doi: 10.1002/ange.201000165 – ident: e_1_2_2_25_2 doi: 10.1039/C0CC04476H – ident: e_1_2_2_9_2 doi: 10.1021/ja310083p – ident: e_1_2_2_11_1 – ident: e_1_2_2_30_2 doi: 10.1021/jacs.5b09920 – ident: e_1_2_2_22_2 doi: 10.1002/chem.200900230 – ident: e_1_2_2_36_1 – ident: e_1_2_2_3_1 – ident: e_1_2_2_17_3 doi: 10.1002/ange.19971091309 – ident: e_1_2_2_17_2 doi: 10.1002/anie.199714401 – ident: e_1_2_2_19_2 doi: 10.1002/(SICI)1521-3773(19990215)38:4<557::AID-ANIE557>3.0.CO;2-S – ident: e_1_2_2_4_2 doi: 10.1021/ja028913b – ident: e_1_2_2_19_3 doi: 10.1002/(SICI)1521-3757(19990215)111:4<512::AID-ANGE512>3.0.CO;2-Y – ident: e_1_2_2_38_2 doi: 10.1021/om500973b – ident: e_1_2_2_28_2 doi: 10.1002/anie.201408652 – ident: e_1_2_2_7_1 – ident: e_1_2_2_39_2 doi: 10.1021/om500729b – ident: e_1_2_2_24_2 doi: 10.1038/nchem.693 – ident: e_1_2_2_8_3 doi: 10.1002/ange.201502983 – ident: e_1_2_2_27_2 doi: 10.1039/c3cs60098j – ident: e_1_2_2_21_2 doi: 10.1021/ja803847w – ident: e_1_2_2_42_1 – ident: e_1_2_2_1_1 doi: 10.1021/cr100357h – ident: e_1_2_2_16_2 doi: 10.1073/pnas.90.12.5394 – ident: e_1_2_2_35_1 doi: 10.1021/cr8005153 – ident: e_1_2_2_28_3 doi: 10.1002/ange.201408652 – ident: e_1_2_2_33_2 doi: 10.1039/b902238b – ident: e_1_2_2_40_2 doi: 10.1021/om101102j – ident: e_1_2_2_12_2 doi: 10.1002/1521-3773(20021104)41:21<4028::AID-ANIE4028>3.0.CO;2-2 – ident: e_1_2_2_13_2 doi: 10.1021/ja0202006 – ident: e_1_2_2_29_2 doi: 10.1039/C3DT53243G – ident: e_1_2_2_20_2 doi: 10.1021/ja992821d – ident: e_1_2_2_8_2 doi: 10.1002/anie.201502983 – ident: e_1_2_2_34_3 doi: 10.1002/ange.200703883 – ident: e_1_2_2_10_1 doi: 10.1021/ja027489b – ident: e_1_2_2_14_2 doi: 10.1073/pnas.0809903106 – ident: e_1_2_2_43_2 doi: 10.1021/ja4032067 – ident: e_1_2_2_32_2 doi: 10.1002/anie.201000165 – ident: e_1_2_2_44_2 doi: 10.1002/anie.201107227 – ident: e_1_2_2_6_2 doi: 10.1039/C4CS00305E – ident: e_1_2_2_26_2 doi: 10.1039/C2CS35123D |
SSID | ssj0028806 |
Score | 2.4676905 |
Snippet | Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type... Highly selective, narcissistic self‐sorting has been observed in the one‐pot synthesis of three organometallic molecular cylinders of type [M 3 {L‐(NHC) 3 } 2... Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M {L-(NHC) } ](PF )... Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type... Highly selective, narcissistic self-sorting has been observed in the one-pot synthesis of three organometallic molecular cylinders of type [M3 {L-(NHC)3 }2... |
SourceID | proquest pubmed crossref wiley |
SourceType | Aggregation Database Index Database Enrichment Source Publisher |
StartPage | 7393 |
SubjectTerms | Benzene Chemical synthesis Coordination compounds Cylinders Fidelity Gold Hydrocarbons Ligands Narcissism narcissistic self-sorting organometallic complexes poly-NHC ligands Silver silver and gold supramolecular chemistry |
Title | High‐Fidelity, Narcissistic Self‐Sorting in the Synthesis of Organometallic Assemblies from Poly‐NHC Ligands |
URI | https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fanie.201702637 https://www.ncbi.nlm.nih.gov/pubmed/28544306 https://www.proquest.com/docview/1907235918 https://www.proquest.com/docview/1903163973 |
Volume | 56 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3NTtwwEB5VXOilBUpLKCBXqsSlgY1_EueIVqy2VbWqukXiFtmOgxC7CWJ3D_TUR-gz8iTMJJvAFlWV6CmJPE6cjMf-HM98A_BRc6uV5Tr0Pe5Cya0NbZSYMNe5wulXOeFqB9lRPDyTX87V-aMo_oYfovvhRpZRj9dk4MbOjh9IQykCm1yzElxFCAonJ4ctQkXfO_4ojp2zCS8SIqQs9C1rY48fr1ZfnZWeQM1V5FpPPYPXYNpGNx4nV0eLuT1yP__gc_yft9qAV0tcyk6ajrQJL3y5Bev9Nh3cG7ghj5C7X78HxIuF0P0TG1EaIjQpYnpmYz8psHRcESvBBbssGSJLNr4t8YAirCpYHfZZTT3C_QnWoO3mqUUIPGMU48K-VZNbvMNo2GdfLy8oAnkbzganP_rDcJmwIXQywQHXGF4YqXKVWKNjo6WRXvGE54b7ONXCKuUTZRHkpEanUvYKXcRxj_sozZ30qXgLa2VV-h1gGoWcQL0ph8OMz41y1sR5pJzhFpeMAYStwjK3ZDOnpBqTrOFh5hl9yaz7kgEcdvLXDY_HXyX3Wv1nS3ueZQibEi5UGukAPnTFqAHaXjGlrxa1jIhon1QE8K7pN92jKE5V4uosAF5r_x9tyE5Gn0-7q93nVHoPL-mcvNqidA_W5jcLv4_4aW4Pahu5B-ZpE9U |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V3NbtQwEB5V5VAu_ENTChgJxIW0GydOnAOHatvVLl0ixLZSb8F2nKpim1TdXaHlxCPwKrwKj8CTMJM_tCCEhNQDpyjxOD_2zHgmnvkG4JnkWgrNpWt73LgB19rVXqTcTGYCl19hfFMFyCbh8Dh4fSJO1uBrmwtT40N0P9xIMip9TQJOP6R3f6KGUgo2xWZF6Eb4URNXeWiXH9Frm70a7eMUP-d8cHDUH7pNYQHXBBEqBqV4rgKRiUgrGSoZqMAKHvFMcRvG0tdC2EhoXIxjJeMg6OUyD8Met16cmcAS_hJq_WtURpzg-vffdYhVHMWhTmjyfZfq3rc4kT2-u_q-q-vgb8btqq1cLXaDm_CtHaY6xuXDzmKud8ynXxAk_6txvAU3GtOb7dWychvWbHEHNvptxbu7cElBL98_fxkQ9Bd6Jy9ZQpWWUGsQmDWb2GmOrZOSgBdO2VnB0Hhmk2WBByRhZc6qzNby3KJHM8UetKN-rtHKnzFK42Fvy-kS75AM-2x8dkpJ1vfg-Eo--T6sF2VhN4FJJDI-MoowqEltpoTRKsw8YRTX6BU74LYckpoGsJ3qhkzTGmqapzRzaTdzDrzo6C9qqJI_Um63DJc2KmuWomUYcV_EnnTgadeMM0A7SKqw5aKi8T3aCvYdeFAzavcoSsUN0AF1gFfs9pd3SPeS0UF3tvUvnZ7AxvDozTgdj5LDh3CdrlMQnxdvw_r8cmEfobk4148rAWXw_qo5-QcwfXDi |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMw1V3NbtQwEB5VrQRcKL9loYCRQFxImzh24hw4VLtd7dJqVbFU6i3YjlNVbJOquyu0nHgEHoVX4RV4EmaSTdCCEBJSD5yixJPEsWfGM_HMNwDPFTdKGq4853PrCW6MZ4JYe5nKJC6_0oa2CpAdRYNj8eZEnqzB1yYXpsaHaH-4kWRU-poE_CLLd3-ChlIGNoVmxehFhPEyrPLALT6i0zZ9PezhDL_gvL__rjvwlnUFPCti1Ata81wLmcnYaBVpJbRwksc809xFiQqNlC6WBtfiRKtECD9XeRT53AVJZoUj-CVU-hsi8hMqFtF72wJWcZSGOp8pDD0qe9_ARPp8d7W_q8vgb7btqqlcrXX9TfjWjFId4vJhZz4zO_bTLwCS_9Mw3oKbS8Ob7dWSchvWXHEHrnebend34ZJCXr5__tIn4C_0TV6xEdVZQp1BUNZs7CY5to5Lgl04ZWcFQ9OZjRcFHpCElTmr8lrLc4f-zATvoP30c4M2_pRREg87KicLfMJo0GWHZ6eUYn0Pjq_kk-_DelEW7gEwhUQ2RD6RFvWoy7S0RkdZIK3mBn3iDngNg6R2CddOVUMmaQ00zVOaubSduQ68bOkvaqCSP1JuN_yWLhXWNEW7MOahTALVgWdtM84A7R_pwpXziiYMaCM47MBWzaftqygRV6D72QFecdtf-pDujYb77dnDf7npKVw76vXTw-Ho4BHcoMsUwRck27A-u5y7x2grzsyTSjwZvL9qRv4BUldvkQ |
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=High%E2%80%90Fidelity%2C+Narcissistic+Self%E2%80%90Sorting+in+the+Synthesis+of+Organometallic+Assemblies+from+Poly%E2%80%90NHC+Ligands&rft.jtitle=Angewandte+Chemie+International+Edition&rft.au=Sinha%2C+Narayan&rft.au=Tan%2C+Tristan+T.+Y.&rft.au=Peris%2C+Eduardo&rft.au=Hahn%2C+F.+Ekkehardt&rft.date=2017-06-19&rft.issn=1433-7851&rft.eissn=1521-3773&rft.volume=56&rft.issue=26&rft.spage=7393&rft.epage=7397&rft_id=info:doi/10.1002%2Fanie.201702637&rft.externalDBID=n%2Fa&rft.externalDocID=10_1002_anie_201702637 |
thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1433-7851&client=summon |
thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1433-7851&client=summon |
thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1433-7851&client=summon |