Journal
JOURNAL OF ORGANIC CHEMISTRY
Volume 70, Issue 25, Pages 10569-10571Publisher
AMER CHEMICAL SOC
DOI: 10.1021/jo051812m
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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 LTV-vis spectra.
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