The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane

碩士 === 國立臺灣大學 === 化學學系 === 81 === The purpose of this work is to investigate the proper synthetic condition under which narrow distributed linear polymethylphenylsiloxane(PMPS) could be synthesized.The assignments of the methyl groups...

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Main Authors: Tsai,Foo-Jung, 蔡馥嶸
Other Authors: Yang,Mei-Hui
Format: Others
Language:zh-TW
Published: 1993
Online Access:http://ndltd.ncl.edu.tw/handle/40329257185510516340
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spelling ndltd-TW-081NTU000650412016-02-10T04:08:58Z http://ndltd.ncl.edu.tw/handle/40329257185510516340 The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane 三甲基三苯基環三矽氧的陰離子聚合反應之研究 Tsai,Foo-Jung 蔡馥嶸 碩士 國立臺灣大學 化學學系 81 The purpose of this work is to investigate the proper synthetic condition under which narrow distributed linear polymethylphenylsiloxane(PMPS) could be synthesized.The assignments of the methyl groups of PMPS on HNMR spectra were also confirmed. In the preparation of narrow molecular weight distributed PMPS, n-BuLi was used as initiator. It was found that narrow molecular weight distributed homopolymers could be obtained through the bulk process under 200C, however backbiting happened and only 81.4% yielded.In solution polymerization, THF and Toluene were used as solvents. It was found that when THF was used both as solvent and promoter under refluxing, narrowly dispersed PMPS could be obtained with high conversion(99.6%) and least backbiting and without chain transfer. The assignments of the methyl groups in the PMPS on proton NMR spectra was done by according to the polymerization mechanisms and the proton NMR analysis. The three peaks of the structures from high field to down field were assigned to be mm,mr,rr. By using molecular model , we found that the reason of the opposite assignments of the methyl groups in the PMPS and poly(α- methyl styrene) could due to the intramolecular compensation in PMPS. Yang,Mei-Hui 楊美惠 1993 學位論文 ; thesis 65 zh-TW
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language zh-TW
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description 碩士 === 國立臺灣大學 === 化學學系 === 81 === The purpose of this work is to investigate the proper synthetic condition under which narrow distributed linear polymethylphenylsiloxane(PMPS) could be synthesized.The assignments of the methyl groups of PMPS on HNMR spectra were also confirmed. In the preparation of narrow molecular weight distributed PMPS, n-BuLi was used as initiator. It was found that narrow molecular weight distributed homopolymers could be obtained through the bulk process under 200C, however backbiting happened and only 81.4% yielded.In solution polymerization, THF and Toluene were used as solvents. It was found that when THF was used both as solvent and promoter under refluxing, narrowly dispersed PMPS could be obtained with high conversion(99.6%) and least backbiting and without chain transfer. The assignments of the methyl groups in the PMPS on proton NMR spectra was done by according to the polymerization mechanisms and the proton NMR analysis. The three peaks of the structures from high field to down field were assigned to be mm,mr,rr. By using molecular model , we found that the reason of the opposite assignments of the methyl groups in the PMPS and poly(α- methyl styrene) could due to the intramolecular compensation in PMPS.
author2 Yang,Mei-Hui
author_facet Yang,Mei-Hui
Tsai,Foo-Jung
蔡馥嶸
author Tsai,Foo-Jung
蔡馥嶸
spellingShingle Tsai,Foo-Jung
蔡馥嶸
The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
author_sort Tsai,Foo-Jung
title The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
title_short The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
title_full The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
title_fullStr The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
title_full_unstemmed The Anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
title_sort anionic polymerization of 1,3,5-trimethyl-1,3,5-triphenyl- cyclotrisiloxane
publishDate 1993
url http://ndltd.ncl.edu.tw/handle/40329257185510516340
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