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紫外光照下C_(60)与聚苯乙烯直接反应合成C_(60)-聚苯乙烯衍生物及电子自旋共振(ESR)研究 被引量:1

Synthesis and ESR Spectrum Study of C_(60)-Polystyrene by Direct Reaction of Polystyrene and C_(60) under UV Photoinitiator
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摘要 在室温 ,紫外光照下溶液相中C60 与聚苯乙烯的直接反应合成得聚苯乙烯的C60 加合物 .衍生物中C60 的含量可由C60的投料比来控制 .得到的产物经UV Vis ,FTIR ,GPC ,TGA及DSC等波谱表征 ,测得产物的分子量比母体聚苯乙烯的分子量稍高 .对溶液相的反应进行了现场的ESR研究 ,得到强的PSC-·60 的自由基信号 ,g值为 2 .0 0 2 4.同时对C60 和聚苯乙烯混合物固相体系的光照反应进行了ESR测试 .结果表明在反应过程中及最终产物中均存在稳定的C60 高分子链烃基自由基阴离子RC-·60 . The C-60 chemically modified polystyrene derivatives were synthesized by direct reaction of a benzene solution of poly styrene and C-60 using UV irradiation at room temperature. The extent of fullerenation can be controlled by varying the C-60 feed mass ratio. The products were characterized by UV-Vis, FTIR, GPC, TGA and DSC techniques. The molecular weights of the C-60-polystyrene derivatives were higher than those of the parent polystyrene. The reaction of C-60 with polystyrene in benzene solution was monitored by electron spin resonance (ESR) spectrum. An intense signal of stable free radical PSC60-. was observed with a g-value of 2.0024. The ESR measurement also was performed in quartz ESR tubes containing a polystyrene/C-60 solid mixture under UV irradiation. All of the samples gave an ESR signal of fullerene polystyrene radical PSC60-., and some ESR signals remained in final solid C-60-PS product after precipitation and drying in air. These results indicated the radical mechanism of the reaction.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2003年第6期954-958,共5页 Acta Chimica Sinica
基金 国家自然科学基金(Nos.2 9890 2 1 6 2 0 2 71 0 1 3)资助项目
关键词 紫外光 C60 聚苯乙烯 直接反应 合成 C60-聚苯乙烯衍生物 电子自旋共振 富勒烯 自由基反应 C-60 free radical reaction electron spin resonance spectrum
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  • 1Allemand, P. M. ; Khemani, K. C. ; Koch, A. ; Wudl, F. ;Holczer, K.; Donovan, S.; Gruner, G.; Thompson, J. D.Science 1991 , 253, 301.
  • 2Tutt, L. W. ; Kost, A. Nature 1992, 356, 225.
  • 3Kajzar, F. ; Taliani, C. ; Danieli, R. ; Rossini, S. ; Zamboni,R. Chem. Phys. Lett. 1994, 217, 418.
  • 4Bunker, C. E.; Lawson, G. E. ; Sun, Y. P. Macromolecules 1995, 28, 3744.
  • 5Stewart, D. ; Imrie, C. T. J. Chem. Soc., Chem. Commun.1996, 1383.
  • 6Wang, C. C. ; Tao, Z. H. ; Hu, J. H. ; Fu, S. K. Chem. J.Chin. Univ. 2000, 21, 805 (in Chinese).
  • 7Tang, B. Z. ; Leung, S. M.; Peng, H. ; Yu, N. T. ; Su, K.C. Macromolecules 1997, 30, 2848.
  • 8Patil, A. 0.; Brois, S. J. Polymer 1997, 38, 3423.
  • 9Qu, B.; Chen, S. M.; Dai, L. M. Appl. Magn. Reson.2000, 19, 59.
  • 10Qu, B.; Hawthorn, G.; Man, A. W. H.; Dai, L. M. J.Phys. Chem. B 2001, 105, 2129.

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