By Helen Zhang, M. Han, X. J. Zhao
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Extra resources for Advanced Research on Material Engineering, Electrical Engineering and Applied Technology II
Vol. 15 (2013), p. 980  H. Nishi and S. Kobatake: Macromolecules. Vol. 41 (2008), p. 3995  Q. F. Luo, H. Cheng and H. Tian: Polylm. Chem. Vol. 2 (2011), p. 2435  R. J. Wang, S. Z. Pu, G. Liu, S. Q. Cui and H. Li: Tetrahedron Lett. Vol. 54 (2013), p. 5307  S. Z. Pu, G. Liu, and J. K. Xu. Org. Lett. Vol. 2139. X. Y. Liao, W. H. Xu, C. J. H. Yan: J. Phys. Chem. C. Vol. 112 (2008), p. 5190S.  N. Tanaka, C. Okabe, K. Sakota, and M. Irie:J. Mol. Struct. Elsevier, Amsterdam. vol. 616(2002),p.
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. Abstract. A photochromic diarylethene of 1-(2-methyl-1-benzofuran-3-yl)-2-(2-methyl-5-(4-benzylamine)-3-thienyl))perfluorocyclopentene was synthesized and characterized. Upon irradiation with UV light with the extended response time, the diarylethene underwent a ring opening reaction to produce opened forms and color change both in solution and in a PMMA amorphous film.
Xu, C. J. H. Yan: J. Phys. Chem. C. Vol. 112 (2008), p. 5190S.  N. Tanaka, C. Okabe, K. Sakota, and M. Irie:J. Mol. Struct. Elsevier, Amsterdam. vol. 616(2002),p. 113. Advanced Materials Research Vol. 23 Research on Photochromic Compounds with Synthesis and Properties of a Novel Unsymmetrical Diarylethene with a Benzothiophene and a Pyrrole Group Hongjing Jia, Yinglong Fu and Congbin Fan * Jiangxi Key Laboratory of Organic Chemistry, Jiangxi Science and Technology Normal University, Nanchang 330013, P.
Advanced Research on Material Engineering, Electrical Engineering and Applied Technology II by Helen Zhang, M. Han, X. J. Zhao