Guanidinium as bifunctional organocatalyst for ring-opening polymerizations

被引:14
作者
Xu, Jiaxi [1 ]
Liu, Jingjing [1 ]
Li, Zhenjiang [1 ]
Wang, Haixin [1 ]
Xu, Songquan [1 ]
Guo, Tianfo [1 ]
Zhu, Hui [1 ]
Wei, Fulan [1 ]
Zhu, Yuejia [1 ]
Guo, Kai [1 ]
机构
[1] Nanjing Tech Univ, Coll Biotechnol & Pharmaceut Engn, 30 Puzhu Rd South, Nanjing 211816, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Acid-base adduct; Hydrogen bonding; Ring-opening polymerization; HYDROGEN-BONDING ORGANOCATALYSTS; L-LACTIDE; LEWIS PAIRS; BULK-POLYMERIZATION; CYCLIC CARBONATES; DUAL ACTIVATION; TERTIARY AMINE; MESO-LACTIDE; CATALYSIS; LACTONES;
D O I
10.1016/j.polymer.2018.08.074
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Typical organocatalyst promoted ring-opening polymerization (ROP) by activation of monomer or polymer chain end via the acidic or basic mechanism. Dual activating of both the monomer and the propagating polymer chain end suggested an ideal strategy of widely tuneable catalysis of high efficiency. Stoichiometric Bronsted acid-base adduct was rarely employed in ROPs since general Bronsted acid and Bronsted base quench each other. We proposed that an acid-base adduct may work bifunctionally in catalysis. The cationic part of the acid-base adduct as H-bond donor activated the monomer, and the counter anion part as H-bond acceptor activated initiator/chain end. A series of guanidiniums, derived from commercially available Bronsted acids and guanidine, were employed as catalysts in ROPs of carbonate, lactide, and lactone. Guanidinium triazabicyclodecene hydrochloride exhibited outstanding catalytic performances in the respect of the rate and controlled in the ROPs of L-lactide, trimethylene carbonate, and delta-valerolactone with nearly full conversions, predicted molecular weights, as well as narrow dispersity of D = 1.07. These experimental results indicated that guanidinium is an efficient organocatalyst in controlled/living ring-opening polymerization.
引用
收藏
页码:17 / 26
页数:10
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