Synthesizes and Properties Research of a Photochromic Diarylethene Bearing a Hexatomic Ring

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Abstract:

A new photochromic diarylethene compound 1-(2-cyan-3-phenyl)-2-[5-(4-cyanobenzene) -2-methyl-3-thienyl] perfluorocyclopentene was synthesized. And their properties inculding photochromis, fluorescence in both hexane and solid films, reaction kinetics of cyclization and cycloreversion were studied. And its absorption maxima were observed at 539 nm in hexane and at 552 nm in PMMA films, respectively, upon irradiation with 313 nm UV light. The fluorescence intensity of diarylethene decreased upon irradiation with 313 nm UV light. Besides, the cyclization and cycloreversion processes of the compound were determined to be the zeroth and first order reaction by UV-Vis spectra, respectively.

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278-281

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October 2013

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© 2014 Trans Tech Publications Ltd. All Rights Reserved

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[1] J.J. Zhang, Q. Zou and H. Tian: Adv. Mater. Vol. 24 (2012), p.1.

Google Scholar

[2] K. Uchida, A. Takata, M. Saito, A. Murakami, S. Nakamura and M. Irie: Adv. Mater. Vol. 15 (2003), p.785.

Google Scholar

[3] S.H. Chen, H.M.P. Chen, Y. Geng, S.D. Jacobs, K.L. Marshall and T. N. Blanton: Adv. Mater. Vol. 15 (2003), p.1061.

Google Scholar

[4] H. Tian, B. Chen, H.Y. Tu and K. Müllen: Adv. Mater. Vol. 14 (2002), p.918.

Google Scholar

[5] A. Fernandez-Acebes and J.M. Lehn: Adv. Mater., Vol. 11 (1999), p.910.

Google Scholar

[6] J.N. Yao, K. Hashimoto and A. Fujishima: Nature, Vol. 355 (1992), p.624.

Google Scholar

[7] M. Irie, S. Kobatake and M. Horichi: Science, Vol. 291 (2001), p.1769.

Google Scholar

[8] S. Kobatake, S. Takami and H. Muto: Nature, Vol. 446 (2007), p.778.

Google Scholar

[9] S.Z. Pu, T.S. Yang and G.Z. Li: Tetrahedron Lett., Vol. 47 (2006), p.3167.

Google Scholar

[10] S.Z. Pu, G. Liu and L. Shen: Org. Lett., Vol. 9 (2007), p.2139.

Google Scholar

[11] S.Z. Pu, T.S. Yang, J.K. Xu, L. Shen, G.Z. Li, Q. Xiao and B. Chen: Tetrahedron Vol 61 (2006), p.6623.

Google Scholar

[12] M. Hoshino, F. Ebisawa, T. Yoshida and K.J. Sukegawa: Photochem. Photobiol., A. Vol 105 (1995), p.75.

Google Scholar

[13] B.Z. Chen, M.Z. Wang and H. Tian: Chem. Commun. Vol. 3 (2002), p.1060.

Google Scholar