The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties
碩士 === 淡江大學 === 化學學系碩士班 === 103 === In this research, new ionic compounds base on 1,10-phenanthroline, L1 and L2 were synthesized with high yield. L1 was synthesised by the reaction of macrocyclic molecule HDPA (bis(1,10-phenanthrolin-2-yl)amine) with 1,6-diiodohexane. The L1 was designed for differ...
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ndltd-TW-103TKU050650092016-08-12T04:14:24Z http://ndltd.ncl.edu.tw/handle/07287019483327756511 The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties 新式含氮橋基雙氮雜菲衍生之化合物合成、結構與性質研究 Hsiang Chang 張翔 碩士 淡江大學 化學學系碩士班 103 In this research, new ionic compounds base on 1,10-phenanthroline, L1 and L2 were synthesized with high yield. L1 was synthesised by the reaction of macrocyclic molecule HDPA (bis(1,10-phenanthrolin-2-yl)amine) with 1,6-diiodohexane. The L1 was designed for different reaction site with HDPA derivatives synthesized in other research. L1 is synthesized by the modification of phenanthroline instead of bridge nitrogen of HDPA and generate an asymmetric structure. L2 was synthesized by the exchange of anion for the solubility. The H-H COSY, HMQC and HMBC technology were used for solving the aromatic signal of L1 and L2. And L1 and L2 were identified by ESI-MS. The acid titration UV-Vis experiments shows Pka of L1 was 3.13 and Pka of L2 was 2.98. The oxidation potential of L1 were -0.19 eV, -0.89 eV and L2 were -0.73 eV, -1.07 eV. The reduction otenrial of L1 were 0.68 eV, 0.93 eV and L2 were 0.76 eV, 0.88 eV. Wen-Jwu Wang 王文竹 2015 學位論文 ; thesis 50 zh-TW |
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碩士 === 淡江大學 === 化學學系碩士班 === 103 === In this research, new ionic compounds base on 1,10-phenanthroline, L1 and L2 were synthesized with high yield. L1 was synthesised by the reaction of macrocyclic molecule HDPA (bis(1,10-phenanthrolin-2-yl)amine) with 1,6-diiodohexane. The L1 was designed for different reaction site with HDPA derivatives synthesized in other research.
L1 is synthesized by the modification of phenanthroline instead of bridge nitrogen of HDPA and generate an asymmetric structure. L2 was synthesized by the exchange of anion for the solubility.
The H-H COSY, HMQC and HMBC technology were used for solving the aromatic signal of L1 and L2. And L1 and L2 were identified by ESI-MS. The acid titration UV-Vis experiments shows Pka of L1 was 3.13 and Pka of L2 was 2.98. The oxidation potential of L1 were -0.19 eV, -0.89 eV and L2 were -0.73 eV, -1.07 eV. The reduction otenrial of L1 were 0.68 eV, 0.93 eV and L2 were 0.76 eV, 0.88 eV.
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Wen-Jwu Wang |
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Wen-Jwu Wang Hsiang Chang 張翔 |
author |
Hsiang Chang 張翔 |
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Hsiang Chang 張翔 The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
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Hsiang Chang |
title |
The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
title_short |
The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
title_full |
The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
title_fullStr |
The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
title_full_unstemmed |
The New Bis(1,10-phenanthrolin-2-yl)amine Derivatives:Synthesis,Structure and Properties |
title_sort |
new bis(1,10-phenanthrolin-2-yl)amine derivatives:synthesis,structure and properties |
publishDate |
2015 |
url |
http://ndltd.ncl.edu.tw/handle/07287019483327756511 |
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