On the cationic photopolymerization of the spiroorthoester
碩士 === 國立臺灣科技大學 === 高分子系 === 95 === A spiro(perhydro-1,3-benzodioxolan-2,2-tetrahydrofuran) (SPBT) underwent cationic double ring-opening phtotopoly-merization instantaneously to afford a poly(2-oxycyclohexyl- butanoate) when it expend to the UV light using diaryl iodonium salt as a photosensitizer...
Main Authors: | , |
---|---|
Other Authors: | |
Format: | Others |
Language: | zh-TW |
Published: |
2007
|
Online Access: | http://ndltd.ncl.edu.tw/handle/w9t792 |
id |
ndltd-TW-095NTUS5310052 |
---|---|
record_format |
oai_dc |
spelling |
ndltd-TW-095NTUS53100522019-05-15T19:47:45Z http://ndltd.ncl.edu.tw/handle/w9t792 On the cationic photopolymerization of the spiroorthoester 螺環原酸酯之陽離子光聚合反應研究 Yen-Shen Wan 萬彥昇 碩士 國立臺灣科技大學 高分子系 95 A spiro(perhydro-1,3-benzodioxolan-2,2-tetrahydrofuran) (SPBT) underwent cationic double ring-opening phtotopoly-merization instantaneously to afford a poly(2-oxycyclohexyl- butanoate) when it expend to the UV light using diaryl iodonium salt as a photosensitizer. By comparing with the cationic polymerization using Lewis acid such as BF3OEt2 and CH3OSO2CF3 as a initiator, SPBT undergoing cationic photopolymerization had a much lower extant of side reaction, and the product, poly(2-oxycyclohexyl butanoate), thus formed had a higher molecular weight and volume expansion. The mechanism of the cationic photopolymerization and the structure determination of the product were studied in detail in this article. Ying-Ghi Hsu 許應舉 2007 學位論文 ; thesis 46 zh-TW |
collection |
NDLTD |
language |
zh-TW |
format |
Others
|
sources |
NDLTD |
description |
碩士 === 國立臺灣科技大學 === 高分子系 === 95 === A spiro(perhydro-1,3-benzodioxolan-2,2-tetrahydrofuran) (SPBT) underwent cationic double ring-opening phtotopoly-merization instantaneously to afford a poly(2-oxycyclohexyl- butanoate) when it expend to the UV light using diaryl
iodonium salt as a photosensitizer. By comparing with the cationic polymerization using Lewis acid such as BF3OEt2 and CH3OSO2CF3 as a initiator, SPBT undergoing cationic photopolymerization had a much lower extant of side reaction, and the product, poly(2-oxycyclohexyl butanoate), thus formed had a higher molecular weight and volume expansion. The mechanism of the cationic photopolymerization and the structure determination of the product were studied in detail in this article.
|
author2 |
Ying-Ghi Hsu |
author_facet |
Ying-Ghi Hsu Yen-Shen Wan 萬彥昇 |
author |
Yen-Shen Wan 萬彥昇 |
spellingShingle |
Yen-Shen Wan 萬彥昇 On the cationic photopolymerization of the spiroorthoester |
author_sort |
Yen-Shen Wan |
title |
On the cationic photopolymerization of the spiroorthoester |
title_short |
On the cationic photopolymerization of the spiroorthoester |
title_full |
On the cationic photopolymerization of the spiroorthoester |
title_fullStr |
On the cationic photopolymerization of the spiroorthoester |
title_full_unstemmed |
On the cationic photopolymerization of the spiroorthoester |
title_sort |
on the cationic photopolymerization of the spiroorthoester |
publishDate |
2007 |
url |
http://ndltd.ncl.edu.tw/handle/w9t792 |
work_keys_str_mv |
AT yenshenwan onthecationicphotopolymerizationofthespiroorthoester AT wànyànshēng onthecationicphotopolymerizationofthespiroorthoester AT yenshenwan luóhuányuánsuānzhǐzhīyánglíziguāngjùhéfǎnyīngyánjiū AT wànyànshēng luóhuányuánsuānzhǐzhīyánglíziguāngjùhéfǎnyīngyánjiū |
_version_ |
1719093927671234560 |