徐铁齐

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:男

毕业院校:吉林大学

学位:博士

所在单位:化学学院

学科:有机化学. 高分子化学与物理

办公地点:大连理工大学化学楼501

联系方式:Email:tqxu@dlut.edu.cn Phone:(0411)84708904

电子邮箱:tqxu@dlut.edu.cn

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Silylium dual catalysis in living polymerization of methacrylates via In situ hydrosilylation of monomer

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论文类型:期刊论文

发表时间:2015-08-15

发表刊物:JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY

收录刊物:SCIE、EI、Scopus

卷号:53

期号:16

页面范围:1895-1903

ISSN号:0887-624X

关键字:living polymerization; methacrylate; hydrosilylation; group-transfer polymerization; silylium catalysts; methyl methacrylate

摘要:Silylium ions (R3Si+) are found to catalyze both 1,4-hydrosilylation of methyl methacrylate (MMA) with R3SiH to generate the silyl ketene acetal initiator in situ and subsequent living polymerization of MMA. The living characteristics of the MMA polymerization initiated by R3SiH (Et3SiH or Me2PhSiH) and catalyzed by [Et3Si(L)](+)[B(C6F5)(4)](-) (L=toluene), which have been revealed by four sets of experiments, enabled the synthesis of the polymers with well-controlled M-n values (identical or nearly identical to the calculated ones), narrow molecular weight distributions (D=1.05-1.09), and well defined chain structures {H[MMA](n)H}. The polymerization is highly efficient too, with quantitative or near quantitative initiation efficiencies (I*=96-100%). Monitoring of the reaction of MMA+Me2PhSiH+[Et3Si(L)](+)[B(C6F5)(4)](-) (0.5 mol%) by H-1 NMR provided clear evidence for in situ generation of the corresponding SKA, Me2CC(OMe)OSiMe2Ph, via the proposed Et3Si+-catalyzed 1,4-hydrosilylation of monomer through frustrated Lewis pair type activation of the hydrosilane in the form of the isolable silylium-silane complex, [Et3SiHSiR3](+)[B(C6F5)(4)](-). (c) 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015, 53, 1895-1903