Functional biodegradable polymers via ring-opening polymerization of monomers without protective groups

被引:183
作者
Becker, Greta [1 ,2 ]
Wurm, Frederik R. [1 ]
机构
[1] Max Planck Inst Polymer Res, Ackermannweg 10, D-55128 Mainz, Germany
[2] Grad Sch Mat Sci Mainz, Staudinger Weg 9, D-55128 Mainz, Germany
关键词
ENE CROSS-LINKING; SUBSTITUTED BETA-PROPIOLACTONES; CRITICAL SOLUTION TEMPERATURE; 6-MEMBERED CYCLIC CARBONATE; BROMO-EPSILON-CAPROLACTONE; ALPHA-HELICAL POLYPEPTIDE; HYDROPHILIC GRAFT CHAINS; ALIPHATIC POLYESTERS; SIDE-CHAIN; N-CARBOXYANHYDRIDE;
D O I
10.1039/c8cs00531a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biodegradable polymers are of current interest and chemical functionality in such materials is often demanded in advanced biomedical applications. Functional groups often are not tolerated in the polymerization process of ring-opening polymerization (ROP) and therefore protective groups need to be applied. Advantageously, several orthogonally reactive functions are available, which do not demand protection during ROP. We give an insight into available, orthogonally reactive cyclic monomers and the corresponding functional synthetic and biodegradable polymers, obtained from ROP. Functionalities in the monomer are reviewed, which are tolerated by ROP without further protection and allow further post-modification of the corresponding chemically functional polymers after polymerization. Synthetic concepts to these monomers are summarized in detail, preferably using precursor molecules. Post-modification strategies for the reported functionalities are presented and selected applications highlighted.
引用
收藏
页码:7739 / 7782
页数:44
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