Bulk Ring-Opening Transesterification Polymerization of the Renewable δ-Decalactone Using an Organocatalyst

被引:96
|
作者
Martello, Mark T. [2 ]
Burns, Adam
Hillmyer, Marc [1 ]
机构
[1] Univ Minnesota, Dept Chem, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN 55455 USA
来源
ACS MACRO LETTERS | 2012年 / 1卷 / 01期
关键词
L-LACTIDE; THERMOPLASTIC ELASTOMERS; TRIBLOCK COPOLYMERS; CHAIN SCISSION; CYCLIC ESTERS; K(P)/K(TR); LACTONES; KINETICS; ACID;
D O I
10.1021/mz200006s
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The bulk ring-opening polymerization of renewable delta-decalactone using 1,5,7-triazabicyclo[4.4.0]dec-5-ene was carried out at temperatures between 7 and 110 degrees C. The equilibrium monomer concentration for reactions within this temperature range was used to determine the polymerization thermodynamic parameters (Delta H-p = -17.1 +/- 0.6 kJ mol(-1), Delta S-p = -54 +/- 2 J mol(-1) K-1) for delta-decalactone. The polymerization kinetics were established and high molar mass poly(delta-decalactone) was prepared with a glass transition temperature of -51 degrees C. Poly(delta-decalactone) samples with controlled molar mass and narrow molar mass distributions were realized by controlling the monomer conversion and initiator concentration. A high molar mass poly(lactide)-poly(delta-decalactone)-poly(lactide) triblock copolymer with a low polydispersity index was prepared by simple sequential addition of monomers. The product triblock exhibited two distinct glass transitions temperatures consistent with microphase segregation.
引用
收藏
页码:131 / 135
页数:5
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