An Annulative Synthetic Strategy for Building Triphenylene Frameworks by Multiple C−H Bond Activations
DC Field | Value | Language |
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dc.contributor.author | Bijoy P. Mathew | - |
dc.contributor.author | Hyun Ji Yang | - |
dc.contributor.author | Joohee Kim | - |
dc.contributor.author | Jae Bin Lee | - |
dc.contributor.author | Yun-Tae Kim | - |
dc.contributor.author | Sungmin Lee | - |
dc.contributor.author | Chang Young Lee | - |
dc.contributor.author | Wonyoung Choe | - |
dc.contributor.author | Kyungjae Myung | - |
dc.contributor.author | Jang-Ung Park | - |
dc.contributor.author | Sung You Hong | - |
dc.date.available | 2018-01-08T05:16:54Z | - |
dc.date.created | 2017-05-19 | - |
dc.date.issued | 2017-04 | - |
dc.identifier.issn | 1433-7851 | - |
dc.identifier.uri | https://pr.ibs.re.kr/handle/8788114/4180 | - |
dc.description.abstract | C−H activation is a versatile tool for appending aryl groups to aromatic systems. However, heavy demands on multiple catalytic cycle operations and site-selectivity have limited its use for graphene segment synthesis. A Pd-catal- yzed one-step synthesis of functionalized triphenylene frameworks is disclosed, which proceeds by 2- or 4-fold C−H arylation of unactivated benzene derivatives. A Pd2(dibenzylideneacetone)3 catalytic system, using cyclic diaryliodonium salts as π-extending agents, leads to site-selective inter- and intramolecular tandem arylation sequences. Moreover, N-substituted triphenylenes are applied to a field-effect transistor sensor for rapid, sensitive, and reversible alcohol vapor detection. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinhei | - |
dc.description.uri | 1 | - |
dc.language | 영어 | - |
dc.publisher | WILEY-V C H VERLAG GMBH | - |
dc.subject | arylation | - |
dc.subject | C−H activation | - |
dc.subject | diaryliodonium salt | - |
dc.subject | palladium | - |
dc.subject | triphenylene | - |
dc.title | An Annulative Synthetic Strategy for Building Triphenylene Frameworks by Multiple C−H Bond Activations | - |
dc.type | Article | - |
dc.type.rims | ART | - |
dc.identifier.wosid | 000399384700018 | - |
dc.identifier.scopusid | 2-s2.0-85016982079 | - |
dc.identifier.rimsid | 59480 | ko |
dc.date.tcdate | 2018-10-01 | - |
dc.contributor.affiliatedAuthor | Bijoy P. Mathew | - |
dc.contributor.affiliatedAuthor | Kyungjae Myung | - |
dc.contributor.affiliatedAuthor | Sung You Hong | - |
dc.identifier.doi | 10.1002/anie.201700405 | - |
dc.identifier.bibliographicCitation | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, v.56, no.18, pp.5007 - 5011 | - |
dc.citation.title | ANGEWANDTE CHEMIE-INTERNATIONAL EDITION | - |
dc.citation.volume | 56 | - |
dc.citation.number | 18 | - |
dc.citation.startPage | 5007 | - |
dc.citation.endPage | 5011 | - |
dc.date.scptcdate | 2018-10-01 | - |
dc.description.wostc | 14 | - |
dc.description.scptc | 13 | - |
dc.description.journalClass | 1 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.subject.keywordPlus | GRAPHENE NANORIBBONS | - |
dc.subject.keywordPlus | CATALYZED ANNULATION | - |
dc.subject.keywordPlus | CARBON NANOTUBES | - |
dc.subject.keywordPlus | PALLADIUM | - |
dc.subject.keywordPlus | NANOGRAPHENE | - |
dc.subject.keywordPlus | NANOSTRUCTURES | - |
dc.subject.keywordPlus | TRANSPARENT | - |
dc.subject.keywordPlus | ARYLATION | - |
dc.subject.keywordPlus | UNIFORM | - |
dc.subject.keywordPlus | ARYNES | - |
dc.subject.keywordAuthor | arylation | - |
dc.subject.keywordAuthor | C-H activation | - |
dc.subject.keywordAuthor | diaryliodonium salt | - |
dc.subject.keywordAuthor | palladium | - |
dc.subject.keywordAuthor | triphenylene | - |