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HomeKey Engineering MaterialsKey Engineering Materials Vols. 474-476Efficient Synthesis and Properties of a...

Efficient Synthesis and Properties of a Photochromic Diarylethene Bearing an Isoxazole Moiety

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Abstract:

A novel photochromic diarylethene based on isoxazole moiety was synthesized and its photochromic and fluorescent properties were also investigated. The compounds exhibited remarkable photochromism, changing from colorless to red after irradiation with UV light both in solution and in PMMA film. The fluorescence had a remarkable initial increase with subsequent dramatic decrease with increasing concentration. The results indicated that the isoxazole moiety played a very important role during the process of photochromic reaction for the diarylethene derivative.

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Advanced Materials and Computer Science

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Periodical:

Key Engineering Materials (Volumes 474-476)

Pages:

1496-1499

DOI:

https://doi.org/10.4028/www.scientific.net/KEM.474-476.1496

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Online since:

April 2011

Authors:

Hong Liang Liu, Shou Zhi Pu, Shi Qiang Cui, Wei Jun Liu

Keywords:

Diarylethene, Fluorescence, Isoxazole, Photochromism, Synthesis

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© 2011 Trans Tech Publications Ltd. All Rights Reserved

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[1] Y. Chen, C.M. Wang, M.G. Fan, B.L. Yao and N. Menke: Opt. Mater. Vol. 26 (2004), p.75.

[2] S.J. Luo, K.X. Chen, L.C. Cao, G.D. Liu, Q.S. He, G.F. Jin, D.X. Zeng and Y. Chen: Opt. Express. Vol. 13 (2005), p.3123.

[3] S.Z. Pu, T.S. Yang, B.L. Yao, Y.L. Wang, M. Lei and J.K. Xu: Mater. Lett. Vol 61 (2007), p.855.

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

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

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

[7] S. Kawata and Y. Kawata: Chem. Rev. Vol. 100 (2000), p.1777.

[8] F.M. Raymo and M. Tomasulo: Chem. Soc. Rev. Vol. 34 (2005), p.327.

[9] S. Takami and M. Irie: Tetrahedron. Vol. 60 (2004), p.6155.

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

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

[12] T. Yamaguchi and M. Irie: Tetrahedron Lett. Vol. 47 (2006), p.1267.

[13] T. Yamaguchi, W. Taniguchi, T. Ozeki, S. Irie and M. Irie: J. Photochem. Photobiol. A. Vol. 207 (2009), p.282.

[14] K. Shibata, L. Kuroki, T. Fukaminato and M. Irie: Chem. Lett. Vol. 37 (2008), p.832.

[15] Z.X. Li, L.Y. Liao, W. Sun, C.H. Xu, C. Zhang, C.J. Fang and C.H. Yan: J. Phys. Chem. C. Vol. 112 (2008), p.5190.

[16] S.Z. Pu, H.H. Tang, B. Chen, J.K. Xu and W.H. Huang: Mater. Lett. Vol. 60 (2006), p.3553.

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

[18] H. Tian, B.Z. Chen, H.Y. Tu and K. Müllen: Adv. Mater. Vol. 17 (2002), p.918.

[19] T. Fukaminato, T. Kawai, S. Kobatake and M. Irie: J. Phys. Chem. B. Vol. 107 (2003), p.8372.