Preparation, structure, and unique redox properties of mono-, bis-, and Tris(diarylmethylene)-1,3,5-trithianes and related compounds

Abstract

A series of 1,3,5-trithianes 1-3 having diarylmethylene units were designed as novel electron donors giving highly colored cationic species upon oxidation. They were prepared along with the dithiane and dithiazine derivatives 4-6 by the reactions of lithiated heterocycles with diaryl ketones followed by dehydration. Voltammetric analyses indicate that a… (More)

Topics

Cite this paper

@article{Suzuki2000PreparationSA, title={Preparation, structure, and unique redox properties of mono-, bis-, and Tris(diarylmethylene)-1,3,5-trithianes and related compounds}, author={Suzuki and Yoshino and Nishida and Ohkita and Tsuji}, journal={The Journal of organic chemistry}, year={2000}, volume={65 18}, pages={5514-21} }