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Photo- and Thermal Interconversion of Multiconfigurational Strained Hydrocarbons Exhibiting Completely Switchable Oxidation to Stable Dicationic Dyes

Press release (in Japanese)

 

Abstract
Highly strained hydrocarbons with two di/tribenzocycloheptatriene units were designed as electrochromic overcrowded ethylenes that undergo reversible interconversion with stable dicationic dyes. Due to severe steric repulsion, two configurational isomers (anti,anti-folded and syn,anti-folded forms) were isolated as stable entities. Photo- and thermal interconversion of these isomers proceeded…..

Read more on Journal of the American Chemical Society

 

Article information:
Ishigaki Y., Hayashi Y., and Suzuki T.,
Photo- and Thermal Interconversion of Multiconfigurational Strained Hydrocarbons Exhibiting Completely Switchable Oxidation to Stable Dicationic Dyes. J. Am. Chem. Soc. 2019, 141, 45, 18293–18300.
DOI: 10.1021/jacs.9b09646