Methacryloyl and/or Hydroxyl End-Functional Star Polymers Synthesized by ATRP Using the Arm-First Method

被引:20
|
作者
Ohno, Shigeki [1 ]
Gao, Haifeng [1 ]
Cusick, Brian [1 ]
Kowalewski, Tomasz [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;
关键词
arm-first method; atom transfer radical polymerization (ATRP); cross-linker; functional star polymers; monomers; TRANSFER RADICAL POLYMERIZATION; CROSS-LINKING MACROMONOMERS; BLOCK-COPOLYMERS; STRUCTURAL CONTROL; GRAFT-COPOLYMERS; CLICK CHEMISTRY; BUTYL ACRYLATE; ARCHITECTURES; POLYSTYRENE; DESIGN;
D O I
10.1002/macp.200800560
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Star polymers with methacryloyl groups at the chain ends were synthesized by esterification of hydroxyl end-functional star polymers. First, the linear hetero-telechelic macroinitiator (MI) was prepared by ATRP using a functional initiator. The obtained MI was chain-extended and cross-linked with DVB and then esterified into methacryloyl. chain-end functionality. The degree of esterification was controlled by changing the initial molar ratios of methacryloyl chloride to hydroxyl groups. The methacryloyl-containing star polymers were cross-linked either intermolecularly or intramolecularly under heating or UV irradiations, depending on the concentrations of star polymers during the cross-linking reactions.
引用
收藏
页码:421 / 430
页数:10
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