Photoinduced cooperative molecular reorientation on azobenzene side-chain-type copolymers
In order to improve the value of photoinduced birefringence and the long-term stability of azobenzene copolymer, two series of azobenzene side-chain-type copolymers consisting of two repeating units, one bearing cyanoazobenzene (or cyanoazopyridine) and the other bearing a long π-conjugated chromoph...
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Published in | Journal of photochemistry and photobiology. A, Chemistry. Vol. 183; no. 3; pp. 273 - 279 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
25.10.2006
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Subjects | |
Online Access | Get full text |
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Summary: | In order to improve the value of photoinduced birefringence and the long-term stability of azobenzene copolymer, two series of azobenzene side-chain-type copolymers consisting of two repeating units, one bearing cyanoazobenzene (or cyanoazopyridine) and the other bearing a long π-conjugated chromophore (bisazobenzene), have been synthesized and compared with respect to their photoinduced birefringence characteristics. Consequently, a fairly large value (observed highest value was 0.244) and superior stability (initial relaxation value was less than 0.2%) of photoinduced birefringence have been achieved. Furthermore, unusual behavior of the photoinduced birefringence depending on the copolymerization ratio of the two chromophores has been found, i.e., a sharp peak of the photoinduced birefringence has been observed at a copolymerization ratio of around 50:50
mol%. This phenomenon could be attributed to mutual promotion of the photoinduced molecular reorientation process, that is cooperative molecular motion, taking place at a specific stoichiometric composition ratio of the two chromophores. |
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ISSN: | 1010-6030 1873-2666 |
DOI: | 10.1016/j.jphotochem.2006.06.012 |