Synthesis, Photochromism and Fluorescence of a Novel Diarylethene Having Thiazole Unit

Article Preview

Abstract:

A new unsymmetrical isomeric diarylethene was synthesized, namely 1-(2,4-dimethyl-5-thiazolyl)-2-[2-methyl-5- (3-methoxyphenyl)-3-thienyl] perfluorocyclopentene (1o). Its photochromic reactivity both in solution and in PMMA film, photoconversion ratio at photostationary state, and fluorescence were investigated in detail. The compound displayed excellent photochromism both in solution and in PMMA film. The isomeric compound also functioned as a fluorescence switch and concentration dependence on the fluorescence spectrum in hexane.

You might also be interested in these eBooks

Info:

Periodical:

Advanced Materials Research (Volumes 455-456)

Pages:

17-20

Citation:

Online since:

January 2012

Export:

Price:

Permissions CCC:

Permissions PLS:

Сopyright:

© 2012 Trans Tech Publications Ltd. All Rights Reserved

Share:

Citation:

[1] M. Irie: Photo-Reactive Materials for Ultrahigh-Density Optical Memory (Elsevier, Amsterdam 1994).

Google Scholar

[2] B.L. Feringa: Molecular Switches (Wiley-VCH Publication, Germany 2001).M.A. Green: High Efficiency Silicon Solar Cells (Trans Tech Publications, Switzerland 1987).

Google Scholar

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

Google Scholar

[4] H. Dürr and H. Bouas-Laurent: Photochromism: Molecules and Systems (Elsevier, Amsterdam 1990).

Google Scholar

[5] M. Irie, T. Lifka, S. Kobatake and N. Kato: J. Am. Chem. Soc. Vol. 122 (2000), p.4871.

Google Scholar

[6] T. Yamaguchi, Y. Fujita, H. Nakazumi, S. Kobatake and M. Irie: Tetrahedron Vol. 60 (2004), p.9863.

DOI: 10.1016/j.tet.2004.08.034

Google Scholar

[7] S. Kobatake and M. Irie: Tetrahedron Vol. 59 (2003), p.8359.

Google Scholar

[8] K. Uchida, Y. Nakayama and M. Irie: Bull. Chem. Soc. Jpn. Vol. 63 (1990), p.1311.

Google Scholar

[9] M. Hanazawa, R. Sumiya, Y. Horikawa and M. Irie: Chem. Commun. (1992), p.206.

Google Scholar

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

Google Scholar

[11] H. Miyasaka, T. Nobuo, A. Itaya, N. Tamai and M. Irie: Chem. Phys. Lett. Vol. 269 (1997), p.281.

Google Scholar

[12] J. Ern, A.T. Bens, H. -D. Martin, S. Mukamel, D. Schmid, S. Tretiak, E. Tsiper and C. Kryschi: Chem. Phys. Vol. 246 (1999), p.115.

DOI: 10.1016/s0301-0104(99)00183-4

Google Scholar

[13] K. Shibata, K. Muto, S. Kobatake and M. Irie: J. Phys. Chem. A. Vol. 106 (2002), p.209.

Google Scholar

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

Google Scholar

[15] G. Liu, S.Z. Pu and X.M. Wang: Tetrahedron Vol. 66 (2010), p.8862.

Google Scholar

[16] K. Kasatani, S. Kambe and M. Irie: J. Photochem. Photobio. A: Chem. Vol. 122 (1999), P. 11.

Google Scholar

[17] B. Gorodetsky, H.D. Samachetty, R.L. Donkers, M.S. Workentin and N.R. Branda: Angew. Chem. Int. Ed, Vol. 43 (2004), p.2812.

DOI: 10.1002/anie.200353029

Google Scholar

[18] T. Fukaminato, T. Sasaki, T. Kawai, N. Tamai and M. Irie: J. Am. Chem. Soc. Vol. 126 (2004), p.14843.

Google Scholar

[19] Z.G. Zhou, H. Yang, M. Shi, S.Z. Xiao, F.Y. Li, T. Yi and C.H. Huang: Chem. Phys. Chem. Vol. 8 (2007), p.1289.

Google Scholar

[20] Y. Gabe, Y. Urano, K. Kikuchi, H. Kojima and T. Nagano: J. Am. Chem. Soc. Vol. 126 (2004), p.3357.

Google Scholar

[21] Y. Liu, N. Zhang, Y. Chen and L.H. Wang: Org. Lett. Vol. 9 (2007), p.315.

Google Scholar

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

Google Scholar