Efficient and Facile End Group Control of Living Ring-Opening Metathesis Polymers via Single Addition of Functional Cyclopropenes

被引:38
作者
Elling, Benjamin R. [1 ]
Xia, Yan [1 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
基金
美国国家科学基金会;
关键词
TRANSFER RADICAL POLYMERIZATION; GLASS-TRANSITION TEMPERATURE; CHAIN-END; BLOCK-COPOLYMERS; HETEROTELECHELIC POLYMERS; TELECHELIC POLYMERS; CLICK CHEMISTRY; ROMP POLYMERS; MACROMONOMERS; COMPLEX;
D O I
10.1021/acsmacrolett.8b00347
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Living ROMP has become an important technique for preparing well-controlled, highly functional polymers; however, installing functional groups at the end of living ROMP polymers is not as straightforward as ROMP itself. We report a simple, efficient strategy to introduce functionalities at the chain end of living polynorbornenes via highly selective single addition of disubstituted 1,1-cyclopropenes (CPEs) with no homopropagation. Unlike many other methods for ROMP chain end functionalization, our method does not result in catalyst termination, allowing for further functionalization after CPE addition. The remarkable reactivity of such CPEs allowed for quantitative chain end functionalization to install a variety of useful functionalities, including halides, aldehydes, ketones, amines, and dyes, without using a large excess of CPEs. These polymer chain ends can be readily modified using a range of postpolymerization modifications.
引用
收藏
页码:656 / 661
页数:11
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