Synthesis and Electrochemical Studies of Carbazoles

碩士 === 國立暨南國際大學 === 應用化學系 === 94 === The abstract altogether divides into two part, the first part mainly is discuss and electrochemical studies of carbazole derivatives. This research characterizes mainly on 3, 6 and 9-position substituent of carbazoles. In this research, the oxidation is irreversi...

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Main Authors: Chiu Su kai, 邱思凱
Other Authors: Yuhlong Oliver Su
Format: Others
Language:zh-TW
Published: 2006
Online Access:http://ndltd.ncl.edu.tw/handle/95129401147099074200
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spelling ndltd-TW-094NCNU05000102016-06-01T04:14:43Z http://ndltd.ncl.edu.tw/handle/95129401147099074200 Synthesis and Electrochemical Studies of Carbazoles 卡唑及其衍生物的合成、電化學及光譜電化學研究 Chiu Su kai 邱思凱 碩士 國立暨南國際大學 應用化學系 94 The abstract altogether divides into two part, the first part mainly is discuss and electrochemical studies of carbazole derivatives. This research characterizes mainly on 3, 6 and 9-position substituent of carbazoles. In this research, the oxidation is irreversible when 3, 6-position don』t have any substituent, on the other hand, there is a redox couple at about E1/2= +1.23 V when that have substituent. It also can prove by spectroelectrochemistry, when we oxidize the compound and will produce a dimer carbazole. The second part the first part of research, the dendrimer derivatives of carbazole, and observe the substitueut effect in electrochemistry. In cyclic voltammetry, we can find two redox couples in oxidative more negatively, electro-withdrawing groups will make potential more positively. In spectroelectrochemistry, the characterization of cation radical has a broad band in near-IR region. By the spectroeletrochemistry studies, we can get different spectrum when we applied the different potential. Yuhlong Oliver Su 蘇玉龍 2006 學位論文 ; thesis 117 zh-TW
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language zh-TW
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sources NDLTD
description 碩士 === 國立暨南國際大學 === 應用化學系 === 94 === The abstract altogether divides into two part, the first part mainly is discuss and electrochemical studies of carbazole derivatives. This research characterizes mainly on 3, 6 and 9-position substituent of carbazoles. In this research, the oxidation is irreversible when 3, 6-position don』t have any substituent, on the other hand, there is a redox couple at about E1/2= +1.23 V when that have substituent. It also can prove by spectroelectrochemistry, when we oxidize the compound and will produce a dimer carbazole. The second part the first part of research, the dendrimer derivatives of carbazole, and observe the substitueut effect in electrochemistry. In cyclic voltammetry, we can find two redox couples in oxidative more negatively, electro-withdrawing groups will make potential more positively. In spectroelectrochemistry, the characterization of cation radical has a broad band in near-IR region. By the spectroeletrochemistry studies, we can get different spectrum when we applied the different potential.
author2 Yuhlong Oliver Su
author_facet Yuhlong Oliver Su
Chiu Su kai
邱思凱
author Chiu Su kai
邱思凱
spellingShingle Chiu Su kai
邱思凱
Synthesis and Electrochemical Studies of Carbazoles
author_sort Chiu Su kai
title Synthesis and Electrochemical Studies of Carbazoles
title_short Synthesis and Electrochemical Studies of Carbazoles
title_full Synthesis and Electrochemical Studies of Carbazoles
title_fullStr Synthesis and Electrochemical Studies of Carbazoles
title_full_unstemmed Synthesis and Electrochemical Studies of Carbazoles
title_sort synthesis and electrochemical studies of carbazoles
publishDate 2006
url http://ndltd.ncl.edu.tw/handle/95129401147099074200
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AT qiūsīkǎi kǎzuòjíqíyǎnshēngwùdehéchéngdiànhuàxuéjíguāngpǔdiànhuàxuéyánjiū
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