A Novel One-Pot Procedure for the Fast and Efficient Conversion of RAFT Polymers into Hydroxy-Functional Polymers

被引:37
作者
Gruendling, Till [1 ,2 ]
Dietrich, Mathias [1 ,3 ]
Barner-Kowollik, Christopher [1 ]
机构
[1] Univ Karlsruhe TH, KIT, Inst Tech Chem & Polymerchem, D-76128 Karlsruhe, Germany
[2] Univ New S Wales, UNSW Analyt Ctr, Bioanalyt Mass Spectrometry Facil, Sydney, NSW 2052, Australia
[3] Fraunhofer Inst Chem Technol, Environm Engn Grp, D-76327 Pfinztal, Germany
关键词
FRAGMENTATION CHAIN TRANSFER; TRANSFER RADICAL POLYMERIZATION; DEFINED BLOCK-COPOLYMERS; ABSOLUTE RATE CONSTANTS; END-GROUP MODIFICATION; MASS-SPECTROMETRY; HYDROCARBON AUTOXIDATION; AMBIENT-TEMPERATURE; VERSATILE APPROACH; MOLECULAR-WEIGHT;
D O I
10.1071/CH09080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report on the successful quantitative transformation of methacrylate and acrylate-type polymers prepared by reversible addition-fragmentation chain transfer (RAFT) polymerization carrying a dithioester-end-group into hydroxy-functional polymers. The simple reaction procedure involves stirring a solution of the dithioester-capped polymer and an azo-initiator in tetrahydrofuran at elevated temperatures (T = 60 degrees C) in the presence of air. This reaction quantitatively yields hydroperoxide functionalities that can be efficiently reduced to hydroxy groups in a one-pot procedure using triphenylphosphine. Size exclusion chromatography-electrospray mass spectrometry was employed to monitor the progress of the reaction. The new backbone-linked hydroxy group provides a versatile anchor for chemical end-group conversions and conjugation reactions with prepared RAFT polymers, which alleviates problems with the rather limited ability of the dithioester-end-group to undergo non-radical transformations.
引用
收藏
页码:806 / 812
页数:7
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