Abstract
Abstract Diarylethene is a photochromic molecule, which is potentially applicable to various optoelectronic devices. In diarylethenes the π-system of the two aryl rings is separated in the open-ring isomer, while the π-system is delocalized throughout the molecule in the closed-ring isomer. Based on this idea the exchange interaction between two nitronyl nitroxide radicals connected by a diarylethene unit was photocontrolled reversibly along with photochromism. The switching efficiency is more than 150-fold and thiophene spacer transmits the interaction more efficiently. When diarylethene dimer is used for the switching unit, the electric circuit-like behavior was observed. Moreover, reversed switching is achieved by reversing the thiophene ring. Magnetochemical and photochemical behavior of the radical-substituted diarylethene is described extensively.
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