期刊文献+

N-苯基马来酰亚胺与环己烯共聚物的制备和表征 被引量:2

SYNTHESIS AND CHARACTERIZATION OF N - PHENYLMALEIMIDE AND CYCLOHEXENE COPOLYMER
下载PDF
导出
摘要 Radical copolymerization of N phenylmaleimide(PHMI) and cyclohexene(CH) was carried out with 2,2 azobisisobutyronitrile(AIBN) in various solvents at 60℃.The copolymer composition was determined by elemental analysis and the results showed that the copolymerization of PHMI with CH in chloroform proceeded in homogeneous system to give an alternating copolymer over a wide range of the comonomer composition in the feed.The presence of the formation of the charge transfer complex(CTC) between PHMI and CH in chloroform was not detected by using UV spectra and 1 H NMR method.The absence of CTC between monomers showed that the ability of electron donor of CH was very weak and the interaction between PHMI and CH was also very weak and it was free monomers participated in propagation in this polymerization system.Monomer reactivity ratios of PHMI with CH was determined by K T method and the results are r 1=0 012, r 2 =0.The copolymer was characterized by IR, 1 H NMR and 13 C NMR spectra and there was cis configuration of CH units in the polymer chains which was determined by analysis for 13 C NMR spectra.In addition,the copolymer of PHMI and CH showed a high glass transition temperature ( T g) and excellent thermal stability ,e.g.,the T g and the initial thermal decomposition temperature ( T d) were 200℃ and 350℃,respectively,for the alternating copolymer of PHMI and CH. Radical copolymerization of N phenylmaleimide(PHMI) and cyclohexene(CH) was carried out with 2,2 azobisisobutyronitrile(AIBN) in various solvents at 60℃.The copolymer composition was determined by elemental analysis and the results showed that the copolymerization of PHMI with CH in chloroform proceeded in homogeneous system to give an alternating copolymer over a wide range of the comonomer composition in the feed.The presence of the formation of the charge transfer complex(CTC) between PHMI and CH in chloroform was not detected by using UV spectra and 1 H NMR method.The absence of CTC between monomers showed that the ability of electron donor of CH was very weak and the interaction between PHMI and CH was also very weak and it was free monomers participated in propagation in this polymerization system.Monomer reactivity ratios of PHMI with CH was determined by K T method and the results are r 1=0 012, r 2 =0.The copolymer was characterized by IR, 1 H NMR and 13 C NMR spectra and there was cis configuration of CH units in the polymer chains which was determined by analysis for 13 C NMR spectra.In addition,the copolymer of PHMI and CH showed a high glass transition temperature ( T g) and excellent thermal stability ,e.g.,the T g and the initial thermal decomposition temperature ( T d) were 200℃ and 350℃,respectively,for the alternating copolymer of PHMI and CH.
出处 《高分子学报》 SCIE CAS CSCD 北大核心 2000年第1期108-110,共3页 Acta Polymerica Sinica
关键词 共聚物 环己烯 PHMI 制备方法 N phenylmaleimide,Cyclohexene,Alternating copolymerization,Copolymer
  • 相关文献

参考文献4

  • 1Li Huaming,Chin Chem Lett,1997年,12卷,8期,1045页
  • 2潘祖仁,高分子化学,1996年,98页
  • 3沈其丰,核磁共振碳谱,1988年,83页
  • 4沈其丰,13C核磁共振及其应用,1986年,89页

同被引文献16

  • 1Kanazawa A;Kanaoka S;Aoshima S.查看详情[J],Journal of the American Chemical Society2013(25):9330-9333.
  • 2Yang H J;Xu J B;Pispas S;Zhang G Z.查看详情[J],MACROMOLECULES20123312-3317.
  • 3Yang H J;Xu J B;Zhang G Z.查看详情[J]Science China(Chemistry),2013l-4.
  • 4Dove A P.查看详情[J],ACS Macro Letters2012(12):1409-1412.
  • 5Mohamed A A;Jebrael F H;Elsabee M Z.查看详情[J],MACROMOLECULES1986(01):32-37.
  • 6Yuan Y;Siegmann A;Narkis M;Bell J P.查看详情[J],Journal of Applied Polymer Science1996(06):1049-1054.
  • 7Rzaev Z M O.查看详情[J],Progress in Polymer Science2000(02):163-217.
  • 8Cheng H;Zhao G;Yan D.查看详情[J],Journal of Polymer Science Part A:Polymer Chemistry,1992,(10):2181-2185.
  • 9Lu Y B;Sun W L;Shen Z Q.查看详情[J],European Polymer Journal2002(07):1275-1279.
  • 10Lu Y B;Sun W L;Shen Z Q.查看详情[J],Journal of Applied Polymer Science2005(04):979-982.

引证文献2

二级引证文献10

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部