具有不同长度间隔基的含联苯基团的侧链液晶聚炔的荧光行为

doi:10.3866/PKU.WHXB20100848

Acta Phys. -Chim. Sin. ›› 2010, Vol. 26 ›› Issue (08): 2281-2285.doi: 10.3866/PKU.WHXB20100848

• PHOTOCHEMISTRY AND SPECTROSCOPY • Previous Articles Next Articles

Fluorescence Behavior of Biphenyl Containing Side-Chain Liquid Crystalline Polyacetylene with Various Lengths of Spacers

YU Zhen-Qiang^1,2, ZHANG Xin¹, LI Zi-Chen¹, CHEN Er-Qiang¹, LAM Jacky W. Y.³, TANG Ben-Zhong³

1. Beijing National Laboratory for Molecular Sciences, Key Laboratory of Polymer Chemistry and Physics of the Ministry of Education, Department of Polymer Science and Engineering, College of Chemistry and Molecular Engineering, Peking University, Beijing 100871, P. R. China;
2. School of Chemistry and Chemical Engineering and Shenzhen Key Laboratory of Functional Polymers, Shenzhen University, Shenzhen 518060, Guangdong Province, P. R. China;
3. Department of Chemistry, The Hong Kong University of Science & Technology, Kowloon, Hong Kong, P. R. China

Received:2010-05-13 Revised:2010-07-08 Published:2010-07-23
Contact: YU Zhen-Qiang, CHEN Er-Qiang E-mail:zqyu@szu.edu.cn; eqchen@pku.edu.cn
Supported by:
The project was supported by the National Natural Science Foundation of China (20129001), the Research Grants Council of Hong Kong, China (CA05/06.SC02) and R/D Fund of Shenzhen University, China (200824).

Abstract

Abstract:

Steady state fluorescence and fluorescence decay of a series of monosubstituted biphenyl containing side- chain liquid crystalline polyacetylenes with different lengths of spacers were investigated. For comparison, a monomer was selected as a model compound. Steady state fluorescence spectra elucidated that the polymers and the monomer showed single fluorescence emission arising from the biphenyl group on the side chain. With decreasing the length of the spacer, the fluorescence intensity of the polymer decreased accordingly. The fluorescence decay showed that the decay of the monomer could be fitted to be a single-exponential decay, while that of the polymers should be fitted to be a triple-exponential decay, which may be originated from the local high concentration induced quenching and the rotational restriction of the side-chain biphenyl groups. Solvent effects illustrated that the interaction between the solvents and the biphenyl groups strengthened with increasing the polarity of the solvents.

Key words: Steady state fluorescence, Monosubstituted polyacetylene, Biphenyl, Fluorescence lifetime, Solvent effect

MSC2000:

O644

YU Zhen-Qiang, ZHANG Xin, LI Zi-Chen, CHEN Er-Qiang, LAM Jacky W. Y., TANG Ben-Zhong. Fluorescence Behavior of Biphenyl Containing Side-Chain Liquid Crystalline Polyacetylene with Various Lengths of Spacers[J].Acta Phys. -Chim. Sin., 2010, 26(08): 2281-2285.

References

[1]. Burroughes, J. H.; Bradley, D. D. C.; Brown, A. R.; Marks, B. N.; Mackay, K.; Friend, R. H.; Burn, P. L.; Holmes, A. B. Nature, 1990, 347: 539
[2]. Pei, Q. B.; Yu, G.; Zhang, C.; Yang, Y.; Heeger, A. J. Science, 1995, 269: 1086
[3]. Grem, G.; Leditzky, G.; Ullrich, B.; Leising, G. Synthetic Metals, 1992, 51: 383
[4]. Liu, J. Z.; Lam, J. W. Y.; Tang, B. Z. Chem. Rev., 2009, 109: 5799
[5]. Akagi, K. Chem. Rev., 2009, 109: 5354
[6]. Lauchlan, L.; Etemad, S.; Chung, T. C.; Heeger, A. J.; MacDiarmid, A. G. Phys. Rev. B, 1981, 24: 3701
[7]. Carter, P. W.; Porter, J. D. Phys. Rev. B, 1991, 43: 14478
[8]. Lee, W. E.; Kim, J. W.; Oh, C. J.; Sakaguchi, T.; Fujiki, M.; Kwak, G. Angew. Chem. Int. Edit., 2010, 49: 1406
[9]. Han, C. C.; Balasubramanian, A. J. Polym. Sci. Part A-Polym. Chem., 2008, 46: 5483
[10]. Dong, Y. P.; Lam, J. W. Y.; Tang, B. Z. Polym. Mater. Sci. Eng., 2001, 84: 616
[11]. Jim, C. K. W.; Qin, A. J.; Lam, J. W. Y.; Hauβler, M.; Tang, B. Z. Polymeric Materials: Science and Engineering, 2007, 96: 414
[12]. Qin, A. J.; Jim, C. K. W.; Tang, Y. H.; Lam, J. W. Y.; Liu, J. Z.; Mahtab, F.; Gao, P.; Tang, B. Z. J. Phys. Chem. B, 2008, 112: 9281
[13]. Scherf, U.; Skothein, T. J.; Elsembaumer, R. L.; Reynolds, J. R. Handbook of conducting polymers. 2nd ed. New York: M. Dekker, 1998
[14]. Huang, H. W.; Horie, K.; Yamashita, T.; Machida, S.; Sone, M.; Tokita, M.; Watanabe, J.; Maeda, Y. Macromolecules, 1996, 29: 3485
[15]. He, X. R.; Liu, H. B.; Wang, N.; Ai, X. C.; Wang, S.; Li, Y. L.; Huang, C. S.; Cui, S.; Li, Y. J.; Zhu, D. B. Macromolecular Rapid Communications, 2005, 26: 721
[16]. Lam, J. W. Y.; Tang, B. Z. Accounts of Chemical Research, 2005, 38: 745
[17]. Lam, J. W. Y.; Tang, B. Z. J. Polym. Sci. Part A-Polym. Chem., 2003, 41: 2607
[18]. Lam, J. W. Y.; Dong, Y. P.; Law, C. C. W.; Li, Z.; Sun, J. Z.; Chen, H. Z.; Zheng, Q.; Kwok, H. S.; Wang, M.; Feng, X. D.; Shen, J. C.; Tang, B. Z. Macromolecules, 2005, 38: 3290
[19]. Lam, J. W. Y.; Qin, A. J.; Dong, Y. P.; Lai, L. M.; Haussler, M.; Dong, Y. Q.; Tang, B. Z. J. Phys. Chem. B, 2006, 110: 21613
[20]. Ye, C.; Xu, G. Q.; Yu, Z. Q.; Lam, J. W. Y.; Jang, J. H.; Peng, H. L.; Tu, Y. F.; Liu, Z. F.; Jeong, K. U.; Cheng, S. Z. D.; Chen, E. Q.; Tang, B. Z. J. Am. Chem. Soc., 2005, 127: 7668
[21]. Geng, J. X.; Zhao, X. G.; Zhou, E. L.; Li, G.; Lam, J. W. Y.; Tang, B. Z. Mol. Cryst. Liq. Cryst., 2003, 399: 17
[22]. Yu, Z. Q.; Liu, J. H.; Zhu, C. Z.; Chen, E. Q.; Lam, J. W. Y.; Tang, B. Z. Acta Polym. Sin., 2010: 783
[23]. Huang, Y. M.; Lam, J. W. Y.; Cheuk, K. K. L.; Ge, W. K.; Tang, B. Z. Macromolecules, 1999, 32: 5976
[24]. Huang, Y. M.; Ge, W. K.; Lam, J. W. Y.; Tang, B. Z. Appl. Phys. Lett., 1999, 75: 4094
[25]. Yu, Z. Q.; Liu, J. H.; Yan, J. J.; Liu, X. B.; Liang, D. H.; Lam, J. W. Y.; Dong, Y. P.; Li, Z. C.; Chen, E. Q.; Tang, B. Z. Macromolecules, 2007, 40: 8342
[26]. Lam, J. W. Y.; Kong, X. X.; Dong, Y. P.; Cheuk, K. K. L.; Xu, K. T.; Tang, B. Z. Macromolecules, 2000, 33: 5027
[27]. Mataga, N.; Kaifu, Y.; Koizumi, M. Bull Chem. Soc. Jpn., 1956, 29: 465
[28]. Lippert, V. E. Z. Electrochem, 1957, 61: 962
[29]. Lackwicz, J. R. Principles of fluorescence spectroscopy. 2nd ed. New York: Plenum Press, 1999
[30]. Ren, Y.; Dong, Y. Q.; Lam, J. W. Y.; Tang, B. Z.; Wong, K. S. Chem. Phys. Lett., 2005, 402: 468

Fluorescence Behavior of Biphenyl Containing Side-Chain Liquid Crystalline Polyacetylene with Various Lengths of Spacers

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