Photoisomerization of some Functional Azobenzene-Containing Metal Complexes with Different Substituted Groups

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Abstract:

In this work, two functional azobenzene-containing metal complexes with different substituted groups have been synthesized and their photoisomerization have also been investigated. It has been found that depending on different substituted groups, the formed azobenzene derivatives showed different properties, indicating distinct regulation of molecular skeletons. Spectral data confirmed commonly the characteristic absorption of substituted groups and aromatic segments in molecular structures. Thermal analysis demonstrated that the structural influence of both compounds in different temperature ranges. The difference of thermal stability is mainly attributed to the formation of Schiff base group and different substituent groups in molecular structure. The photoisomerization of these compounds both in solution and in cast film can undergo trans-to-cis isomerization by UV light irradiation, depending on different substituted groups. The present results have demonstrated that the special properties of azobenzene derivatives can be effectively turned by modifying molecular structures of objective compounds with proper substituted groups, which show potential application in sensor and functional material field.

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Advanced Materials Research (Volumes 581-582)

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453-456

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October 2012

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© 2012 Trans Tech Publications Ltd. All Rights Reserved

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[1] T. Yamamoto, Y. Umenmura, O. Sato and Y. Einaga: Chem. Mater. Vol. 16 (2004), p.1195.

Google Scholar

[2] T. Hugel and N.B. Holland: Science Vol. 296 (2002), p.1103.

Google Scholar

[3] H. Nakano, T. Tanino, T. Takahashi, H. Ando and Y. Shirota: J. Mater. Chem. Vol. 18 (2008), p.242.

Google Scholar

[4] C.J. Barrett, J. Mamiya, K.G. Yager and T. Ikeda: Soft Matter Vol. 3 (2007), p.1249.

Google Scholar

[5] S. Kawamura, T. Tsutsui, S. Saito, Y. Murao and K. Kina: J. Am. Chem. Soc. Vol. 110 (1988), p.509.

Google Scholar

[6] L. Rousso, N. Friedman, M. Sheves and M. Ottolenghi: Biochemistry Vol. 34 (1995), p.12059.

Google Scholar

[7] T. Jiao and M. Liu: J. Colloid Interf. Sci. Vol. 299 (2006), p.815.

Google Scholar

[8] T. Jiao and M. Liu: Langmuir Vol. 22 (2006), p.5005.

Google Scholar

[9] M.R. Han and M. Hara: New J. Chem. Vol. 30 (2006), p.223.

Google Scholar

[10] N. Koumura, M. Kudo and N. Tamaoki: Langmuir Vol. 20 (2004), p.9897.

Google Scholar

[11] H. Sapper, D.G. Cameron and H.H. Mantsch: Can. J. Chem. Vol. 59 (1981), p.2543.

Google Scholar

[12] R.G. Snyder, S.L. Hsu and S. Krimm: Spectrochim. Acta. A Vol. 34 (1978), p.395.

Google Scholar

[13] T. Jiao and M. Liu: J. Phys. Chem. B Vol. 109 (2005), p.2532.

Google Scholar

[14] M.F. Yin, T.F. Jiao and M.H. Liu: Chin. Chem. Lett. Vol. 18 (2007), p.30.

Google Scholar