Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9326
Title: Tetracyanoethylene substituted triphenylamine analogues
Authors: Misra, Rajneesh
Mobin, Shaikh M.
Keywords: aniline derivative;tetracyanoethylene;triphenylamine derivative;tris (4 phenylethynylphenyl)amine;unclassified drug;Article;chemical modification;cyclization;cycloaddition;intramolecular charge transfer;retroelectrocyclization;synthesis;temperature
Issue Date: 2014
Publisher: Elsevier Ltd
Citation: Misra, R., Maragani, R., Gautam, P., & Mobin, S. M. (2014). Tetracyanoethylene substituted triphenylamine analogues. Tetrahedron Letters, 55(51), 7102-7105. doi:10.1016/j.tetlet.2014.10.148
Abstract: A set of tetracyanoethylene (TCNE) substituted triphenylamine analogues (4-6) exhibiting strong intramolecular charge transfer (ICT) were designed and synthesized by the [2+2] cycloaddition-retroelectrocyclization reaction of 3 (tris-(4-phenylethynyl-phenyl)-amine) with TCNE. The reaction was found to be temperature dependent. The blue shift in the π → π∗ transition and intramolecular charge transfer (ICT) in amines 4-6 were found to be directly proportional to the number of TCNE units. The computational study shows good agreement with the experimental results and reveals that as the number of TCNE units in amine increases, HOMO-LUMO gap increases. © 2014 Elsevier Ltd. All rights reserved.
URI: https://doi.org/10.1016/j.tetlet.2014.10.148
https://dspace.iiti.ac.in/handle/123456789/9326
ISSN: 0040-4039
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

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