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HomeApplied Mechanics and MaterialsApplied Mechanics and Materials Vol. 164Photochromic Properties of...

Photochromic Properties of 1-[2-Methyl-5-(4-Chlorophenyl)-3-Thienyl]-2-[2-Methyl-5-(Phenanthren-10-Yl)-3-Thienyl]Perfluorocyclopentene

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Abstract:

A novel photochromic diarylethene, 1-[2-methyl-5-(4-chlorophenyl)-3-thienyl]-2-[2-methyl-5-(phenanthren-10-yl)-3-thienyl]perfluorocyclopentene was synthesized and its photochromic and fluorescent properties were also investigated. The compound exhibited remarkable photochromic, changing from colorless to blue after irradiation with UV light both in solution and in PMMA film

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Applied Mechanics, Materials, Industry and Manufacturing Engineering

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Applied Mechanics and Materials (Volume 164)

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255-258

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https://doi.org/10.4028/www.scientific.net/AMM.164.255

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Online since:

April 2012

Authors:

Xue Li, Cong Bin Fan, Gang Liu

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Diarylethene, Fluorescence, Photochromism, Synthesis

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] M. Irie: Chem. Rev. Vol. 100 (2000)，p.1685.

[2] H. Tian, S. Yang: J. Chem. Soc. Rev. Vol. 33 (2004), p.85.

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

[4] S. Kobatake, S. Takami, H. Muto, T. Ishikawa and M. Irie: Nature. Vol. 446 (2007), p.778.

[5] H. Dürr, H. Bouas-Laurent: Elsevier. (1990).

[6] M. Irie, M. Mohri: J. Org. Chem. Vol. 53 (1988), p.803.

[7] T. Kaieda, S. Kobatake, H. Miyasaka, M. Murakami, N. Iwai, Y.I. Nagata,A. Itaya and M. Irie: J. Am. Chem. Soc. Vol. 124 (2002), p. (2015).

DOI: 10.1021/ja0115722

[8] N. Tamai, T. Saika, T. Shimidzu and M. Irie: J. Phys. Chem. Vol. 100 (1996), p.4689.

[9] S. Kobatake, K. Uchida, E. Tsuchida and M. Irie: Chem. Commun. Vol. 23 (2002), p.2804.

[10] K. Matsuda, M. Irie, J. Photochem. Photobiol. C: Photochem. Rev. Vol. 5 (2004), p.169.

[11] S. Takami, M. Irie: Elsevier B. V. Vol. 60 (2004), p.6155.

[12] K. Uchida, T. Ishikawa, M. Takeshita, and M. Irie: Elsevier B. V. Vol. 54 (1998), p.6627.

[13] G. Liu, S. Z. Pu and X. M. Wang: Elsevier B. V. Vol. 66 (2010), p.8862.

[14] K. Yagi, M. Irie: Bull. Chem. Soc. Jpn. Vol. 76 (2003), p.1625.

[15] T. Yamaguchi, M. Irie: J. Org. Chem. Vol. 70 (2005), p.10323.

[16] T. Yamaguchi, Y. Fujita, H. Nakazumi, S. Kobatake and M. Irie, Elsevier B. V. Vol. 60 (2004), p.9863.

[17] S. Z. Pu, G. Liu, Q. Shen and J. K. Xu: Org. Lett. Vol. 9 (2007), p.2139.

[18] T. Yamaguchi, M. Irie: Elsevier B. V. Vol. 47 (2006), p.1267.

[19] G. Li, T. Zheng, S.Z. Pu and J.K. Xu: Acta Cryst. E. Vol. 62 (2006), p. o2877.

[20] S.Z. Pu, H.H. Tang, B. Chen, J.K. Xu and W.H. Huang: Mater. Lett. Vol. 60 (2002), p.3553.

[21] H. Tian, B.Z. Chen, H.Y. Tu and K. Müllen, Adv. Mater. Vol. 17 (2002), p.915.

[22] B. Chen, M. Wang, Y. Wu and H. Tian, Chem. Commun. Vol. 21 (2002), p.1060.