Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives
碩士 === 國立臺灣科技大學 === 纖維及高分子工程技術研究所 === 85 === In this study, Synthesis and application of Mono(Di)-methine quinoline heterocyclic derivatives. Quinoline was reacted with ethyl(amyl) iodide to give 1-substituted-2(4)-methyl quinoline, resulted in producing a series of Mono(Di)-methine and Aza- m...
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ndltd-TW-085NTUS35660152016-07-01T04:15:47Z http://ndltd.ncl.edu.tw/handle/01104416602051339795 Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives 單(雙)-次甲基口奎口林雜環衍生物合成與應用性的研究 曹雪雄 碩士 國立臺灣科技大學 纖維及高分子工程技術研究所 85 In this study, Synthesis and application of Mono(Di)-methine quinoline heterocyclic derivatives. Quinoline was reacted with ethyl(amyl) iodide to give 1-substituted-2(4)-methyl quinoline, resulted in producing a series of Mono(Di)-methine and Aza- methine quinoline heterocyclic derivatives. In part one, quinoline was condensed with terephthalaldehyde to give a series of Di-methine quinoline derivatives, which leads to a series of violet to purplish blue coloured. In part two, quinoline was condensed with heterocyclic compounds of keton structure to give a series of Mono(Di)-methine quinoline derivatives, which leads to a series of reddish purple to purplish blue coloured. In part three, quinoline was condensed with nitrosoaniline derivatives to give a series of Aza-methine quinoline derivatives, which leads to a series of purplish blue to blue coloured. In part four, quinoline was condensed with aromatic aldehyde to give a series of Mono-methine quinoline derivatives, which leads to a series of purplish red to purplish blue coloured. The identification of the structure of the those heterocyclic compounds were confirmed by IR, Mass, UV, H-NMR, EA spectra analysis. These quinoline dyes are suitable for dyeing of PAN fabrics, to proceed tested and appraised of the hues to use (A.C.S.), ranging from reddish purple to blue. 王英靖 1997 學位論文 ; thesis 147 zh-TW |
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碩士 === 國立臺灣科技大學 === 纖維及高分子工程技術研究所 === 85 ===
In this study, Synthesis and application of Mono(Di)-methine quinoline heterocyclic derivatives. Quinoline was reacted with ethyl(amyl) iodide to give 1-substituted-2(4)-methyl quinoline, resulted in producing a series of Mono(Di)-methine and Aza- methine quinoline heterocyclic derivatives.
In part one, quinoline was condensed with terephthalaldehyde to give a series of Di-methine quinoline derivatives, which leads to a series of violet to purplish blue coloured.
In part two, quinoline was condensed with heterocyclic compounds of keton structure to give a series of Mono(Di)-methine quinoline derivatives, which leads to a series of reddish purple to purplish blue coloured.
In part three, quinoline was condensed with nitrosoaniline derivatives to give a series of Aza-methine quinoline derivatives, which leads to a series of purplish blue to blue coloured.
In part four, quinoline was condensed with aromatic aldehyde to give a series of Mono-methine quinoline derivatives, which leads to a series of purplish red to purplish blue coloured.
The identification of the structure of the those heterocyclic compounds were confirmed by IR, Mass, UV, H-NMR, EA spectra analysis. These quinoline dyes are suitable for dyeing of PAN fabrics, to proceed tested and appraised of the hues to use (A.C.S.), ranging from reddish purple to blue.
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王英靖 |
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王英靖 曹雪雄 |
author |
曹雪雄 |
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曹雪雄 Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
author_sort |
曹雪雄 |
title |
Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
title_short |
Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
title_full |
Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
title_fullStr |
Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
title_full_unstemmed |
Synthesis and Application of Mono(Di)-Methine Quinoline Heterocyclic Derivatives |
title_sort |
synthesis and application of mono(di)-methine quinoline heterocyclic derivatives |
publishDate |
1997 |
url |
http://ndltd.ncl.edu.tw/handle/01104416602051339795 |
work_keys_str_mv |
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