Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s
碩士 === 國立交通大學 === 應用化學系 === 87 === Nucleophilic aromatic substitution polymerization of type monomers 4-[2-(4-Flourophenyl)-5-(4-hydroxyphenyl)-1,3-oxazol-4-yl]phenol and 3-[2-(4-fluorophenyl)-4-(3-hydroxyphenyl)-1,3-oxazol-5-yl]phenol,using K2CO3 as reagent and DMPU(1,3-Dimethyl-3,4,5,6-tetrahydro...
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ndltd-TW-087NCTU05000472016-07-11T04:13:50Z http://ndltd.ncl.edu.tw/handle/43370143372889003735 Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s 含有雜環高分枝狀芳香族聚醚類的合成與研究 Zhi-hao Gong 龔智豪 碩士 國立交通大學 應用化學系 87 Nucleophilic aromatic substitution polymerization of type monomers 4-[2-(4-Flourophenyl)-5-(4-hydroxyphenyl)-1,3-oxazol-4-yl]phenol and 3-[2-(4-fluorophenyl)-4-(3-hydroxyphenyl)-1,3-oxazol-5-yl]phenol,using K2CO3 as reagent and DMPU(1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone) as solvent yielded hyperhranched(aryl ether oxazole)s PAEO(Ⅰ) and PAEO(Ⅱ),respectively. The reactivity of two aryl fluoride mononers used in nucleophilic aromatic substitution polymerization was explored utilizing 19F-NMR experiments. The 19F shifts reflect the reactivity of the individual monomers examined. The hyperbranched marcomolecules contain a large number of chain end function groups, and the physical properties of the polymers such as thermal property and solubility depend on the nature of the chain ends. The degree of branching of PAEO(Ⅰ) was determined with the help of model compounds using 1H-NMR and was found to be near 52% ,similar to what has been observed in other hyperbranched polymer systems. Ching-fong Shu 許慶豐 1999 學位論文 ; thesis 97 zh-TW |
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碩士 === 國立交通大學 === 應用化學系 === 87 === Nucleophilic aromatic substitution polymerization of type monomers 4-[2-(4-Flourophenyl)-5-(4-hydroxyphenyl)-1,3-oxazol-4-yl]phenol and 3-[2-(4-fluorophenyl)-4-(3-hydroxyphenyl)-1,3-oxazol-5-yl]phenol,using K2CO3 as reagent and DMPU(1,3-Dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone) as solvent yielded hyperhranched(aryl ether oxazole)s PAEO(Ⅰ) and PAEO(Ⅱ),respectively. The reactivity of two aryl fluoride mononers used in nucleophilic aromatic substitution polymerization was explored utilizing 19F-NMR experiments. The 19F shifts reflect the reactivity of the individual monomers examined. The hyperbranched marcomolecules contain a large number of chain end function groups, and the physical properties of the polymers such as thermal property and solubility depend on the nature of the chain ends. The degree of branching of PAEO(Ⅰ) was determined with the help of model compounds using 1H-NMR and was found to be near 52% ,similar to what has been observed in other hyperbranched polymer systems.
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author2 |
Ching-fong Shu |
author_facet |
Ching-fong Shu Zhi-hao Gong 龔智豪 |
author |
Zhi-hao Gong 龔智豪 |
spellingShingle |
Zhi-hao Gong 龔智豪 Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
author_sort |
Zhi-hao Gong |
title |
Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
title_short |
Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
title_full |
Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
title_fullStr |
Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
title_full_unstemmed |
Synthesis and Characterization of Hyperbranched poly(aryl ether oxazole)s |
title_sort |
synthesis and characterization of hyperbranched poly(aryl ether oxazole)s |
publishDate |
1999 |
url |
http://ndltd.ncl.edu.tw/handle/43370143372889003735 |
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