Organopolymerization of naturally occurring Tulipalin B: a hydroxyl-functionalized methylene butyrolactone

被引:11
|
作者
Tang, Jing [1 ]
Chen, Eugene Y. -X. [1 ]
机构
[1] Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA
来源
ORGANIC CHEMISTRY FRONTIERS | 2015年 / 2卷 / 12期
基金
美国国家科学基金会;
关键词
N-HETEROCYCLIC CARBENES; GROUP-TRANSFER POLYMERIZATION; RING-OPENING POLYMERIZATION; RADICAL COPOLYMERIZATION KINETICS; FRUSTRATED LEWIS PAIRS; TO-TAIL DIMERIZATION; GAMMA-BUTYROLACTONE; CONJUGATE-ADDITION; STEREOSELECTIVE POLYMERIZATION; ANIONIC-POLYMERIZATION;
D O I
10.1039/c5qo00262a
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The first successful polymerization of the naturally occurring, OH-containing, tri-functional monomer Tulipalin B (pHMBL) is established. N-Heterocyclic carbene and phosphazene superbase catalysts effectively polymerize pHMBL into polymers with Mr, up to 13.2 kg morl. The possible polymer structure is thought to be a branched copolymer of poly(vinyl-ether lactone)s, derived from proposed crossovers between conjugate Michael and oxa-Michael additions, enabled by proton transfer.
引用
收藏
页码:1625 / 1631
页数:7
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