Stereoregularities of Ring-containing Polymethacrylates Obtained by Radical Polymerization
Stereoregularities of Ring-containing Polymethacrylates Obtained by Radical Polymerization
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自由基聚合获得的含环聚甲基丙烯酸酯的立构规整性
DOI:
10.1295/polymj.2.555
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发表时间:
1971
期刊:
影响因子:
--
通讯作者:
Y. Sakaguchi
中科院分区:
文献类型:
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作者:
J. Nishino;H. Nakahata;Y. Sakaguchi
Phenyl, 2-naphthyl(2-Np-MA), 1-naphthyl(1-Np-MA), 9-fluorenyl, 5,6,7, 8-tetrahydro-1-naphthyl, cyclohexyl(CH-MA), cyclopentyl(CP-MA), and decahydro-2-naphthyl(D-MA) methacrylates were polymerized in bulk, benzene, and n-hexane by radical initiators. The polymers were converted into poly (methyl methacrylate)(PMMA) by hydrolysis followed by methylation. The tacticities of the polymers were studied by comparing the IR and NMR spectra of the derived PMMA’s. The polymers containing aromatic substituents were more isotactic than conventional PMMA, and especially poly(2-Np-MA) prepared in n-hexane and poly(1-Np-MA)’s were considerably isotactic. On the other hand, tacticities of poly(CH-MA)’s, poly(CP-MA)’s, and poly(D-MA)’s were nearly the same as those of conventional PMMA. These results suggest that aromatic rings of the methacrylates seem to promote the formation of isotactic sequence and this effect is enhanced with naphthyl groups, but the aliphatic rings have little effect on such stereoregulation.
DOI:
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发表时间:
2015
期刊:
影响因子:
--
作者:
前田拓磨;林友貴;澤野弘明;石原進
通讯作者:
石原進