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1 November 2006 Photochemical Behavior of Some p-Styrylstilbenes and Related Compounds: Spectral Properties and Photoisomerization in Solution and in Solid State
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Abstract

The spectral properties and Z,E-photoisomerizations of three 4-styrylstilbenes, a 4,4′-bis(β-methylstyryl)benzene and a 4,4′-distyrylstilbene were investigated in solution and in the solid state. Some notable features of the absorption and fluorescence spectra due to the structures and the phases (solution or solid) were observed, especially the Stokes shifts. Interesting photochemical behaviors in solution and in the solid state were also found. While the (E,Z)-4-styrylstilbenes undergo a one-way photoisomerization to their E,E-isomers with almost equal rates in solution, their quantum yields in the solid state decrease with increasing substituent size at the terminal aromatic rings. On the other hand, the 4,4′-bis(β-methylstyryl)benzene undergoes a mutual photoisomerization in solution, but its E,Z-isomer isomerizes in a one-way manner to the E,E-isomer in the solid state. Additionally, the (Z,E,Z)-4,4′-styrylstilbene was found to undergo a one-way photoisomerization to the E,E,E-isomer via the E,E,Z-isomer in solution and the crystalline E,E,Z-isomer to the E,E,E-isomer in the solid state.

Zhu Fengqiang, Jiro Motoyoshiya, Junji Nakamura, Yoshinori Nishii, and Hiromu Aoyama "Photochemical Behavior of Some p-Styrylstilbenes and Related Compounds: Spectral Properties and Photoisomerization in Solution and in Solid State," Photochemistry and Photobiology 82(6), 1645-1650, (1 November 2006). https://doi.org/10.1562/2006-01-17-RA-780
Received: 17 January 2006; Accepted: 1 July 2006; Published: 1 November 2006
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