Photoinduced reorientation of azo-dyes covalently linked to a styrene copolymer in bulk state

Citation
K. Tawa et al., Photoinduced reorientation of azo-dyes covalently linked to a styrene copolymer in bulk state, J PHOTOCH A, 143(1), 2001, pp. 31-38
Citations number
38
Categorie Soggetti
Physical Chemistry/Chemical Physics
Journal title
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
ISSN journal
10106030 → ACNP
Volume
143
Issue
1
Year of publication
2001
Pages
31 - 38
Database
ISI
SICI code
1010-6030(20011001)143:1<31:PROACL>2.0.ZU;2-I
Abstract
Polarized light-induced orientation in azo-dyes covalently bonded to styren e copolymer (Azo-PSCMS) was investigated by using polarized UV-VIS spectros copy. It was found that thermal isomerization and photoisomerization was sl ower and a photoinduced dichroism was larger than azo-dyes doped in polysty rene. The covalent linkage to a polymer chain may suppress both the mobilit y required for the isomerization and the rotational diffusion of the azo-mo iety. The trans --> cis photoisomerization was induced by ultraviolet (UV) light, whereas light with visible wavelength was used to drive the trans <- ---> cis photoisomerization. A high repetition of "trans-cis-trans" isomeri zation cycles achieved under visible light plays an important role for the photoinduced reorientation. Therefore, the high repetition of the "trans-ci s-trans" cycle and suppression of the rotational diffusion by the covalent linkage to a polymer are the two important factors for the photoinduced reo rientation of azo-dyes in bulk polymer matrix. (C) 2001 Elsevier Science B. V. All rights reserved.