Constructing star polymers via modular ligation strategies

被引:141
作者
Altintas, Ozcan [1 ]
Vogt, Andrew P. [1 ]
Barner-Kowollik, Christopher [1 ]
Tunca, Umit [2 ]
机构
[1] KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Istanbul Tech Univ, Dept Chem, TR-34469 Istanbul, Turkey
关键词
LIVING RADICAL POLYMERIZATION; ONE-POT SYNTHESIS; FRAGMENTATION CHAIN TRANSFER; RING-OPENING POLYMERIZATION; ALDER CLICK REACTION; DRUG-LOADING CAPACITY; DIELS-ALDER; BLOCK-COPOLYMERS; THIOL-ENE; MACROMOLECULAR ARCHITECTURES;
D O I
10.1039/c1py00249j
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Branched polymers result in a more compact structure in comparison to linear polymers of identical molecular weight, due to their high segment density which affects the crystalline, mechanical, and viscoelastic properties of the polymer. Star polymers constitute the simplest form of branched macromolecules where all of the chains-or arm segments-of one macromolecule are linked to a centre defined as the core. Over recent years, modular ligation reactions-some of which adhere to click criteria-have enabled the synthesis of a variety of star polymers via efficient polymer-polymer conjugations. While the modified Huisgen [3 + 2] dipolar copper catalyzed azide and alkyne cycloaddition (CuAAC) has been widely employed for macromolecular star synthesis, Diels-Alder and hetero Diels-Alder reactions offer alternative pathways which allow for similarly efficient macromolecular conjugations. Moreover, combinations of these protocols afford the synthesis of more complex star polymer structures which previously had not been achievable.
引用
收藏
页码:34 / 45
页数:12
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