Advanced Research on Material Engineering, Electrical by Helen Zhang, M. Han, X. J. Zhao

By Helen Zhang, M. Han, X. J. Zhao

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Sample text

Launay, J. Phys. Chem. B Vol. 109 (2005) ,p. 17445-17459 [10] M. Munakata, J. Han, M. Maekawa, Y. Suenaga, T. Kuroda-Sowa, A. Nabei, H. Ebisu: Inorganica Chimica Acta Vol. 360 (2007), p. 2792 [11] (a) H. Tian, L. Y. Feng: J. Mater. Chem. Vol. 18 (2008), p. 1617–1622 ; (b) B. Li, J. Y. Wang, H. M. Wen, L. X. Shi, Z. N. Chen: J. Am. Chem. Soc. Vol. 134 (2012), p. B. Z. Pu, G. S. Yan: J. Photochem. and Photobio. A: Chem. Vol. 194 (2008), p. 333. Advanced Materials Research Vol. com Keywords: Diarylethene; Synthesis; Photochromism; Fluorescence; Kinetics.

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The emission intensity of diarylethene 1c in a photostationary state was quenched to ca. 9% in hexane and ca. 1% in PMMA film. The cyclization reaction which is not complete and the existence of parallel conformations may be the main cause for the moderate change in fluorescence induced by photoirradiation. The reversible changes of the emission intensity of diarylethene 1 are useful for application as the fluorescence switches [14,15]. 0 × 10-4 mol/L) (A) and in PMMA (10%, w/w) (B) with 297 nm UV light.

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