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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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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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 |
work_keys_str_mv |
AT chiusukai synthesisandelectrochemicalstudiesofcarbazoles AT qiūsīkǎi synthesisandelectrochemicalstudiesofcarbazoles AT chiusukai kǎzuòjíqíyǎnshēngwùdehéchéngdiànhuàxuéjíguāngpǔdiànhuàxuéyánjiū AT qiūsīkǎi kǎzuòjíqíyǎnshēngwùdehéchéngdiànhuàxuéjíguāngpǔdiànhuàxuéyánjiū |
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