Standing on the shoulders of hermann staudinger: Post-polymerization modification from past to present

被引:331
作者
Guenay, Kemal Arda [2 ,3 ]
Theato, Patrick [1 ]
Klok, Harm-Anton [2 ,3 ]
机构
[1] Univ Hamburg, Inst Tech & Macromol Chem, D-20146 Hamburg, Germany
[2] Ecole Polytech Fed Lausanne, Inst Mat, Lab Polymeres, CH-1015 Lausanne, Switzerland
[3] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, Lab Polymeres, CH-1015 Lausanne, Switzerland
关键词
click chemistry; functional polymers; polymer analogous reaction; polymerization; reactive monomers; modification; living polymerization; LIVING RADICAL POLYMERIZATION; RING-OPENING POLYMERIZATION; ELECTRON-SPIN-RESONANCE; FRAGMENTATION CHAIN TRANSFER; INDUCED ADDITION-REACTION; DIELS-ALDER-REACTIONS; FLUORINATED KETONE GROUPS; CROSS-COUPLING REACTIONS; WELL-DEFINED POLYMERS; ONE-POT SYNTHESIS;
D O I
10.1002/pola.26333
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
With a span as long as the history of polymer science itself, post-polymerization modification represents a versatile platform for the preparation of diversely functionalized polymers from a single precursor. Starting with the initial efforts by Staudinger in the 1920s, many of the early developments in modern polymer science can be attributed to the utilization of post-polymerization modification reactions. The scope of post-polymerization modification has greatly expanded since the 1990s due to the development of functional group tolerant controlled/living polymerization techniques combined with the (re)discovery of highly efficient coupling chemistries that allow quantitative, chemoselective, and orthogonal functionalization of reactive polymer precursors. After some basic mechanistic considerations, this Highlight will provide an overview of the development and evolution of eight main classes of post-polymerization modification reactions. (C) 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013
引用
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页码:1 / 28
页数:28
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