| Literature DB >> 16323873 |
Kazuo Takimiya1, Yasushi Konda, Hideaki Ebata, Naoto Niihara, Tetsuo Otsubo.
Abstract
[reaction, structures: see text] A general and convenient synthesis of benzo[1,2-b:4,5-b']dichalcogenophenes including the thiophene (BDT, 1), selenophene (BDS, 2), and tellurophene (BDTe, 3) homologues is developed. Thus synthesized heterocycles are structurally characterized by single-crystal X-ray analysis, and all three homologues are isostructural with one another. They all have completely planar molecular structures packed in a herringbone arrangement. Their physicochemical properties were also elucidated by means of cyclic voltammetry (CV) and UV-vis spectra.Entities:
Year: 2005 PMID: 16323873 DOI: 10.1021/jo051812m
Source DB: PubMed Journal: J Org Chem ISSN: 0022-3263 Impact factor: 4.354