Controllable radical copolymerization of styrene and methyl methacrylate using 1,1,2,2-tetraphenyl-1,2-bis(trimethylsilyloxy) ethane as initiator

被引:8
作者
Guo, ZR
Yang, GJ
Wan, DC
Huang, JL [1 ]
机构
[1] Fudan Univ, Dept Macromol Sci, Key Open Lab Mol Engn Polymer, State Educ Minist China, Shanghai 200433, Peoples R China
[2] Second Mil Med Univ, Sch Pharm, Shanghai 200433, Peoples R China
关键词
controllable radical copolymerization; styrene; methyl methacrylate; 1,1,2,2-tetraphenyl-1,2-bis (trimethylsilyloxy) ethane;
D O I
10.1002/app.1986
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Copolymerization of styrene (St) and methyl methacrylate (MMA) was carried out using 1,1,2,2-tetraphenyl-1,2-bis (trimethylsilyloxy) ethane (TPSE) as initiator; the copolymerization proceeded via a "living" radical mechanism and the polymer molecular weight (M-w) increased with the conversion and polymerization time. The reactivity ratios for TPSE and azobisisobutyronitrile (AIBN) systems calculated by Finemann-Ross method were r(St) = 0.216 +/- 0.003, r(mmA)= 0.403 +/- 0.01 for the former and r(St) 0.52 +/- 0.01, r(MMA)= 0.46 +/- 0.01 for the latter, respectively, and the difference between them and the effect of polymerization conditions on copolymerization are discussed. Thermal analysis proved that the copolymers obtained by TPSE system showed higher sequence regularity than that obtained by the AIBN system, and the sequence regularity increased with the content of styrene in copolymer chain segment. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:1474 / 1482
页数:9
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