Detailed Information

Cited 0 time in webofscience Cited 0 time in scopus
Metadata Downloads

Novel dimeric leuco-TAM dyes, 1,4-bis{(1E,3Z)-1,3-bis (1,3,3-trimethylindolin-2-ylidene)propan-2-yl}benzene derivatives: Structure and spectroscopic characterization

Full metadata record
DC Field Value Language
dc.contributor.authorKeum, Sam-Rok-
dc.contributor.authorMa, So-Young-
dc.contributor.authorKim, Do-Kyung-
dc.contributor.authorLim, Hyun-Woo-
dc.contributor.authorRoh, Se-Jung-
dc.date.accessioned2021-09-06T20:48:37Z-
dc.date.available2021-09-06T20:48:37Z-
dc.date.created2021-06-18-
dc.date.issued2012-04-25-
dc.identifier.issn0022-2860-
dc.identifier.urihttps://scholar.korea.ac.kr/handle/2021.sw.korea/108655-
dc.description.abstractNovel dimeric leuco-triarylmethane (LTAM) dyes, 1,4-bis((1E,3Z)-1,3-bis(1,3,3-trimethylindolin-2-ylidene)propan-2-yl}benzene derivatives, as precursors of dimeric TAM(++) and TAM(++) dyes, were synthesized and characterized by 1D and 2D NMR experiments including DEPT, COSY, HSQC, HMBC and NOESY. Judging from the 1H NMR analysis, the dimeric LTAM molecules were suggested to have a dual-propeller shaped structure. For the prepared dimeric leuco-TAM dyes, the ZE/EZ isomers were formed as the sole products from the reaction of 2-3 M excess Fischer base and terephthalaldehyde in absolute ethanol. The ZE/EZ isomers were equilibrated with other diastereomers (EE/EE and ZZ/ZZ) in organic solvents. UV-Vis spectroscopy of dimeric TAM(++) dyes in organic solvents show an absorption band at >700 nm in the near-infrared (NIR) region. Formation of the dimeric TAM(++) molecules was further confirmed by comparison of CV diagrams for monomeric TAM(++) and dimeric TAM(++) molecules. (C) 2012 Elsevier B.V. All rights reserved.-
dc.languageEnglish-
dc.language.isoen-
dc.publisherELSEVIER-
dc.subjectTRIPHENYLMETHANE DYES-
dc.subjectMALACHITE GREEN-
dc.subjectTRIARYLMETHANES-
dc.subjectMETABOLITES-
dc.titleNovel dimeric leuco-TAM dyes, 1,4-bis{(1E,3Z)-1,3-bis (1,3,3-trimethylindolin-2-ylidene)propan-2-yl}benzene derivatives: Structure and spectroscopic characterization-
dc.typeArticle-
dc.contributor.affiliatedAuthorKeum, Sam-Rok-
dc.identifier.doi10.1016/j.molstruc.2012.02.002-
dc.identifier.scopusid2-s2.0-84863391292-
dc.identifier.wosid000302762100019-
dc.identifier.bibliographicCitationJOURNAL OF MOLECULAR STRUCTURE, v.1014, pp.126 - 133-
dc.relation.isPartOfJOURNAL OF MOLECULAR STRUCTURE-
dc.citation.titleJOURNAL OF MOLECULAR STRUCTURE-
dc.citation.volume1014-
dc.citation.startPage126-
dc.citation.endPage133-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Physical-
dc.subject.keywordPlusTRIPHENYLMETHANE DYES-
dc.subject.keywordPlusMALACHITE GREEN-
dc.subject.keywordPlusTRIARYLMETHANES-
dc.subject.keywordPlusMETABOLITES-
dc.subject.keywordAuthorDimeric leuco-TAM-
dc.subject.keywordAuthorTAM(++)-
dc.subject.keywordAuthorDual-propeller shaped structure-
dc.subject.keywordAuthorDiastereomer-
dc.subject.keywordAuthorZE/EZ isomer-
dc.subject.keywordAuthorNear-infrared region-
Files in This Item
There are no files associated with this item.
Appears in
Collections
College of Science and Technology > Department of Advanced Materials Chemistry > 1. Journal Articles

qrcode

Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.

Altmetrics

Total Views & Downloads

BROWSE