Marrying click chemistry with polymerization: expanding the scope of polymeric materials

被引:777
作者
Golas, Patricia L. [1 ]
Matyjaszewski, Krzysztof [1 ]
机构
[1] Carnegie Mellon Univ, Dept Chem, Pittsburgh, PA 15213 USA
基金
美国安德鲁·梅隆基金会; 美国国家科学基金会;
关键词
TRANSFER RADICAL POLYMERIZATION; FRAGMENTATION CHAIN TRANSFER; OPENING METATHESIS POLYMERIZATION; ONE-POT SYNTHESIS; BLOCK-COPOLYMERS; RAFT POLYMERIZATION; ELECTRON-TRANSFER; GRAFT-COPOLYMERS; STAR POLYMERS; HYPERBRANCHED POLYTRIAZOLES;
D O I
10.1039/b901978m
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Click chemistry constitutes a class of reactions broadly characterized by efficiency, selectivity, and tolerance to a variety of solvents and functional groups. By far the most widely utilized of these efficient transformation reactions is the Cu-I-catalyzed azide-alkyne cycloaddition. This reaction has been creatively employed to facilitate the preparation of complex macromolecules, such as multiblock copolymers, shell or core cross-linked micelles, and dendrimers. This critical review highlights the application of click chemistry, in particular the Cu-I-catalyzed azide-alkyne cycloaddition, to the synthesis of a wide variety of new materials with possible uses as drug delivery agents, tissue engineering scaffolds, and dispersible nanomaterials (83 references).
引用
收藏
页码:1338 / 1354
页数:17
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