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http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/48263完整後設資料紀錄
| DC 欄位 | 值 | 語言 |
|---|---|---|
| dc.contributor.advisor | 劉貴生(Guey-Sheng Liou) | |
| dc.contributor.author | Hung-Ju Yen | en |
| dc.contributor.author | 顏宏儒 | zh_TW |
| dc.date.accessioned | 2021-06-15T06:50:35Z | - |
| dc.date.available | 2016-02-01 | |
| dc.date.copyright | 2011-02-20 | |
| dc.date.issued | 2011 | |
| dc.date.submitted | 2011-02-16 | |
| dc.identifier.citation | CHAPTER 1
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| dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/48263 | - |
| dc.description.abstract | 本論文分成五個章節,第一章為總體序論。第二章以3種二胺4,4'-diamino-4'-cyanotriphenylamine、N,N-bis(4-aminophenyl)-N',N'-di(4-cyanophenyl)-1,4-phenylenediamine及 N,N'-bis(4-aminophenyl)-N,N'-di(4-cyanophenyl)-1,4-phenylenediamine與不同二酸合成三系列之新型芳香族聚(胺-醯胺)。第三章節描述了三系列之芳香族聚(胺-醯亞胺),係以二述二胺及不同種二酸酐經一步法或二步聚合法所合成。第四章是以實驗製得之含三苯胺的雙馬來醯亞胺與市售二硫醇經Michael聚加成反應獲得聚醯亞胺硫醚。第五章節為結論及未來工作。這些含氰基芳香胺之高分子的合成、基本特性、光致發光、電學、電化學及電致變色性質皆被研究與比較。所有的高分子在極性非質子型溶劑中都有好的溶解性、出色的薄膜成形能力、高的玻璃轉換溫度、好的熱穩定性,及適當的HOMO值。在利用電化學與光譜電化學的方法下,大部分的高分子也展現優良的電致變色可逆性。這些含氰基芳香胺的高分子由於適當的HOMO值、出色熱穩定性、螢光量子效率及電化學不僅能被做為電洞傳輸層和發光材料,而且也可應用於新型的電致變色元件。 | zh_TW |
| dc.description.abstract | This study has been separated into five chapters. Chapter 1 is general introduction. Chapter 2 includes three series of novel aromatic poly(amine-amide)s derived from synthesized diamines, 4,4'-diamino-4'-cyanotriphenylamine, N,N-bis(4-aminophenyl)-N',N'-di(4-cyanophenyl)-1,4-phenylenediamine, and N,N'-bis(4-aminophenyl)-N,N'-di(4-cyanophenyl)-1,4-phenylenediamine, and various dicarboxylic acids by direct polycondensation. Chapter 3 describes three series of aromatic poly(amine-imide)s prepared from the diamines and various tetracarboxylic dianhydrides via one-step and conventional two-step polymerization. Chapter 4 includes a series of polyimidothioethers prepared from new triphenylamine-based bismaleimides and commercial dithiols via Michael polyaddition. Chapter 5 contains conclusions and future work. The synthesis, basic characterization, photoluminescent, electrical, electrochemical, and electrochromic properties of these aromatic cyanoarylamine-based polymers were investigated and compared. All polymers revealed good solubility in many polar aprotic solvents with excellent thin-film-forming ability. In additional to high Tg values, good thermal stability, high luminecence, and proper HOMO energy levels, most of the obtained polymers also revealed good reversibility of electrochromic characteristics by the electrochemical and spectroelectrochemical methods. Thus, these cyanoarylamine-containing polymers can be considered not only as hole-transporting layer and light-emitting materials but also could be widely applied as new electrochromic devices due to their proper HOMO values, excellent thermal stability, fluorescence quantum efficiency and good electrochemical behavior. | en |
| dc.description.provenance | Made available in DSpace on 2021-06-15T06:50:35Z (GMT). No. of bitstreams: 1 ntu-100-D96549005-1.pdf: 3510107 bytes, checksum: fdca2a80e9090617c710ebcaa8c1edcc (MD5) Previous issue date: 2011 | en |
| dc.description.tableofcontents | CHAPTER 1
General Introduction 1.1 HIGH PERFORMANCE POLYMERS 2 1.1.1 Preparation of Aromatic Polyamides 4 1.1.2 Preparation of Aromatic Polyimides 7 1.1.3 Modification of Aromatic Polyamides and Polyimides 10 1.2 EVOLUTION OF ELECTROCHROMISM 14 1.3 ELECTROCHROMIC SYSTEMS 17 1.3.1 Transition-metal Oxides 17 Tungsten Trioxide (WO3) 17 Iridium Oxide (IrO2) 19 1.3.2 Coordination Complexes 20 Phthalocyanines 20 1.3.3 Organic Molecules 21 Viologens 21 1.3.4 Conducting Polymers 22 1.3.5 Arylamine-based Polymers 24 1.4 AGGREGATION-INDUCED EMISSION ENHANCEMENT (AIEE) 28 1.5 RESEARCH MOTIVATION 29 REFERENCES AND NOTES 31 CHAPTER 2 Synthesis, Luminescence, and Electrochromism of Cyanoarylamine-based Aramids ABSTRACT OF CHAPTER 2 42 2.1 INTRODUCTION 43 2.2 EXPERIMENTAL SECTION 44 2.2.1 Materials 44 2.2.2 Monomer Synthesis 45 4-Amino-4',4'-dicyanotriphenylamine (2) 45 N,N-Bis(4-nitrophenyl)-N',N'-di(4-cyanophenyl)-1,4-phenylenediamine (3) 45 N,N-Bis(4-aminophenyl)-N',N'-di(4-cyanophenyl)-1,4-phenylenediamine (4) 46 N,N'-Bis(4-nitrophenyl)-N,N'-di(4-cyanophenyl)-1,4-phenylenediamine (5) 47 N,N'-Bis(4-aminophenyl)-N,N'-di(4-cyanophenyl)-1,4-phenylenediamine (6) 48 2.2.3 Polymer Synthesis 48 2.2.4 Preparation of the Polyamide Films 49 2.2.5. Measurements 50 2.3 RESULTS AND DISCUSSION 52 2.3.1 Mononer Synthesis 52 2.3.2 Polymer Synthesis 57 2.3.3 Polymer Properties 61 2.3.3.1 Solubility and Film Property 61 2.3.3.2 Thermal Properties 62 2.3.3.3 Optical Properties 66 2.3.3.4 Aggregation-Induced Emission Enhancement (AIEE) 71 2.3.3.5 Electrochemical Properties 73 2.3.3.6 Spectroelectrochemistry and Electrochromic Properties 76 2.4 SUMMARY 79 REFERENCES AND NOTES 80 CHAPTER 3 Synthesis, Luminescence, and Electrochromism of Cyanoarylamine-based Polyimides ABSTRACT OF CHAPTER 3 83 3.1 INTRODUCTION 84 3.2 EXPERIMENTAL SECTION 86 3.2.1 Materials 86 3.2.2 Preparation of Polyimides by Two-Step Method 86 3.2.3 Preparation of Polyimides by One-Step Method 87 3.2.4 Preparation of the Polyimide Films 87 3.2.5. Measurements 88 3.3 RESULTS AND DISCUSSION 90 3.3.1 Polymer Synthesis 90 3.3.2 Polymer Properties 94 3.3.2.1 Basic Characterization 94 3.3.2.2 Electrical Properties 96 3.3.2.3 Optical Properties 98 3.3.3.4 Electrochemical Properties 100 3.3.2.5 Electrochromic Characterization 104 3.4 SUMMARY 107 REFERENCES AND NOTES 108 CHAPTER 4 RGB Electrochromic and Luminescent Polyimidothioethers Based on Cyanoarylamine Units ABSTRACT OF CHAPTER 4 110 4.1 INTRODUCTION 111 4.2 EXPERIMENTAL SECTION 113 4.2.1 Materials 113 4.2.2 Monomer Synthesis 113 4,4'-Bismaleimido-4'-cyanotriphenylamine (CN-BMI) 113 N,N-Bis(4-maleimidophenyl)-N',N'-bis(4-cyanophenyl)-1,4-phnylenediamine (2CN-BMI) 114 4.2.3 Polymer Synthesis 115 4.2.4 Preparation of the PITE Films 116 4.2.5. Measurements 116 4.3 RESULTS AND DISCUSSION 118 4.3.1 Mononer Synthesis 118 4.3.2 Polymer Synthesis 123 4.3.3 Polymer Properties 126 4.3.3.1 Basic Characterization 126 4.3.3.2 Optical Properties 129 4.3.3.3 Electrochemical Properties 132 4.3.3.4 Spectroelectrochemistry and Electrochromic Properties 135 4.4 SUMMARY 139 REFERENCES AND NOTES 140 | |
| dc.language.iso | en | |
| dc.subject | 三苯胺 | zh_TW |
| dc.subject | 電致變色 | zh_TW |
| dc.subject | 螢光 | zh_TW |
| dc.subject | 聚醯亞胺硫醚 | zh_TW |
| dc.subject | 聚醯亞胺 | zh_TW |
| dc.subject | 聚醯胺 | zh_TW |
| dc.subject | 氰 | zh_TW |
| dc.subject | polyimide | en |
| dc.subject | polyamide | en |
| dc.subject | triphenylamine | en |
| dc.subject | cyano | en |
| dc.subject | electrochromic | en |
| dc.subject | fluorescent | en |
| dc.subject | polyimidothioether | en |
| dc.title | 具氰基芳香胺基團功能性芳香族高分子之設計、合成、性質探討及其應用 | zh_TW |
| dc.title | Design, Synthesis, Characterization, and Applications of Functional Aromatic Polymers Based on Cyano-Arylamine Moieties | en |
| dc.type | Thesis | |
| dc.date.schoolyear | 99-1 | |
| dc.description.degree | 博士 | |
| dc.contributor.oralexamcommittee | 蕭勝輝(Sheng-Huei Hsiao),蘇玉龍(Yuhlong Oliver Su),梁文傑(Man-kit Leung),鄭如忠(Ru-Jong Jeng),許聯崇(Steve Lien-Chung Hsu),陳志堅(Jyh-Chien Chen) | |
| dc.subject.keyword | 氰,三苯胺,聚醯胺,聚醯亞胺,聚醯亞胺硫醚,螢光,電致變色, | zh_TW |
| dc.subject.keyword | cyano,triphenylamine,polyamide,polyimide,polyimidothioether,fluorescent,electrochromic, | en |
| dc.relation.page | 154 | |
| dc.rights.note | 有償授權 | |
| dc.date.accepted | 2011-02-16 | |
| dc.contributor.author-college | 工學院 | zh_TW |
| dc.contributor.author-dept | 高分子科學與工程學研究所 | zh_TW |
| 顯示於系所單位: | 高分子科學與工程學研究所 | |
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