Controlled chain-growth polymerization via propargyl/allenyl palladium intermediates

被引:0
|
作者
Wang, Zheng-Lin [1 ]
Zhu, Rong [1 ]
机构
[1] Peking Univ, Coll Chem & Mol Engn, Beijing Natl Lab Mol Sci BNLMS, Key Lab Bioorgan Chem & Mol Engn,Minist Educ, Beijing, Peoples R China
基金
中国国家自然科学基金; 北京市自然科学基金;
关键词
RING-OPENING POLYMERIZATION; CATALYZED ALLYLIC SUBSTITUTION; PI-ALLYLPALLADIUM COMPLEX; MULTIBRANCHING POLYMERIZATION; PROPARGYLIC CARBONATES; CYCLIC CARBAMATE; POLYCONDENSATION; POLYMERS; NUCLEOPHILES; DERIVATIVES;
D O I
10.1038/s41467-025-57723-8
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
In contrast to allyl palladium complexes, propargylic/allenylic palladium species display complex reactivities that limit their implementation in polymer chemistry, especially for chain-growth polymerizations. Here we report an example of controlled chain-growth polymerization via propargyl/allenyl palladium intermediates. Vinylidenecyclopropane 1,1-dicarboxylate (VDCP), a unique allenylic electrophile, selectively reacts via the sigma-allenyl palladium complex rather than the more common pi-propargyl pathway, thereby unlocking a chain-growth process. Based on this concept, precise synthesis of alkyne-backbone polymers is realized, featuring fast rate, high molecular weight, narrow dispersity, high chemoselectivity, and excellent end-group fidelity. We demonstrate preparation of unsaturated macromolecules with advanced sequences and architectures using this method, including block, gradient, and graft copolymers.
引用
收藏
页数:8
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