Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole
碩士 === 國立成功大學 === 化學系碩博士班 === 91 === In this thesis the luminescent organic material was synthesized using carbazole as a starting material and KMnO4 as a cyclization reagent. The structure, physical and electroluminiecent properties for the obtained products including carbazole series and their ind...
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ndltd-TW-091NCKU50650262015-10-13T17:02:34Z http://ndltd.ncl.edu.tw/handle/32977857187737798000 Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole 9-取代-3-(5-芳香基-[1,3,4]oxadiazole-2-基)-9氫-carbazole之合成及發光性質研究 Ing-Ju Li 李盈儒 碩士 國立成功大學 化學系碩博士班 91 In this thesis the luminescent organic material was synthesized using carbazole as a starting material and KMnO4 as a cyclization reagent. The structure, physical and electroluminiecent properties for the obtained products including carbazole series and their indole derivatives were studied by the analysis of NMR elemental analysis IR, DSC,TGA,UV-VIS,CV,PL spectrum and EL test. For the thermal stability , all synthesized compounds had good thermal decomposition temperatures ,but low glass transition temperatures. The result for PL spectrum analysis indicated that substituted groups for the compounds with a long chain on N position effect the PL spectrum but with benzyl group on N position not. The EL device was fabricated by depositing as a film in vacumn and tested to emit too instantly to gain the EL spectrum . This was attributed to the larger velocity for hole-transport than electron-transport. This can be modified by adding the material which can lower the velocity of hole-transport or enhancing the thickness of the deposited film for emitting layer. Mou-Yung Yeh 葉茂榮 2003 學位論文 ; thesis 110 zh-TW |
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碩士 === 國立成功大學 === 化學系碩博士班 === 91 === In this thesis the luminescent organic material was synthesized using carbazole as a starting material and KMnO4 as a cyclization reagent. The structure, physical and electroluminiecent properties for the obtained products including carbazole series and their indole derivatives were studied by the analysis of NMR elemental analysis IR, DSC,TGA,UV-VIS,CV,PL spectrum and EL test.
For the thermal stability , all synthesized compounds had good thermal decomposition temperatures ,but low glass transition temperatures.
The result for PL spectrum analysis indicated that substituted groups for the compounds with a long chain on N position effect the PL spectrum but with benzyl group on N position not.
The EL device was fabricated by depositing as a film in vacumn and tested to emit too instantly to gain the EL spectrum . This was attributed to the larger velocity for hole-transport than electron-transport.
This can be modified by adding the material which can lower the velocity of hole-transport or enhancing the thickness of the deposited film for emitting layer.
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author2 |
Mou-Yung Yeh |
author_facet |
Mou-Yung Yeh Ing-Ju Li 李盈儒 |
author |
Ing-Ju Li 李盈儒 |
spellingShingle |
Ing-Ju Li 李盈儒 Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
author_sort |
Ing-Ju Li |
title |
Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
title_short |
Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
title_full |
Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
title_fullStr |
Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
title_full_unstemmed |
Studies on the Synthesis and Light-Emitting Properties of 9-Substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9H-carbazole |
title_sort |
studies on the synthesis and light-emitting properties of 9-substituted-3-(5-aryl-[1,3,4]oxadiazol-2-yl)-9h-carbazole |
publishDate |
2003 |
url |
http://ndltd.ncl.edu.tw/handle/32977857187737798000 |
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