spirooxazine photoisomerization and relaxation in polymer matrices在聚合物矩阵spirooxazine光异构化和放松.pdfVIP

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spirooxazine photoisomerization and relaxation in polymer matrices在聚合物矩阵spirooxazine光异构化和放松.pdf

spirooxazine photoisomerization and relaxation in polymer matrices在聚合物矩阵spirooxazine光异构化和放松

Hindawi Publishing Corporation International Journal of Polymer Science Volume 2011, Article ID 627195, 6 pages doi:10.1155/2011/627195 Research Article Spirooxazine Photoisomerization and Relaxation in Polymer Matrices Maria Larkowska,1 Michael Wuebbenhorst,2 and Stanislaw Kucharski1 1 Department of Polymer Engineering and Technology, Wrocław University of Technology, 50-370 Wrocław, Poland 2 Department of Physics and Astronomy, Catholic University Leuven, 3001 Heverlee, Belgium Correspondence should be addressed to Stanislaw Kucharski, stanislaw.kucharski@pwr.wroc.pl Received 21 March 2011; Accepted 17 June 2011 Academic Editor: Qijin Zhang Copyright © 2011 Maria Larkowska et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. 9 -Hydroxy-1,3,3-trimethylspiro[indoline-2,3 [3H ]naphtha[2,1-b]-1,4oxazine] (SPO-7OH) was used in studies of photochromic transformations in polymer matrices. Illumination with UV lamp caused opening the spirostructure of the oxazine with formation of open merocyanine species absorbing at ca. 610 nm. The kinetic studies of thermal relaxation of the open form showed that this process can be described with a biexponential function including both photochemical reaction and rheological behaviour of the polymeric environment. Basing on Arrhenius plot of the rate constant ascribed to the photochemical reaction, the activation energy was determined, which was 66.1 and 84.7 kJ/mole for poly(methyl methacrylate-co-butyl methacrylate) and poly(vinylpyrrolidone) matrix, respectively. 1. In

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