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Heterotriangulenes π-Expanded at Bridging Positions

Authors :
Shigehiro Yamaguchi
Shohei Saito
Chih-Ming Chou
Source :
Organic Letters. 16:2868-2871
Publication Year :
2014
Publisher :
American Chemical Society (ACS), 2014.

Abstract

A series of nitrogen-containing heterotriangulenes expanded at the bridging positions has been synthesized. Among them, a dibenzo[c,g]fluorenylidene-substituted derivative has a highly twisted conformation for the overcrowded alkene moieties, which impart a highly electron-accepting character to the electron-donating heterotriangulene skeleton and thereby an NIR absorption as well as multiredox properties with a low reduction potential.

Details

ISSN :
15237052 and 15237060
Volume :
16
Database :
OpenAIRE
Journal :
Organic Letters
Accession number :
edsair.doi.dedup.....d003621bbbf318152a9690ff92216d26
Full Text :
https://doi.org/10.1021/ol501004g