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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
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dc.contributor.advisor | 蔡蘊明 | |
dc.contributor.author | Nung-Sen Wang | en |
dc.contributor.author | 王農森 | zh_TW |
dc.date.accessioned | 2021-06-13T04:24:15Z | - |
dc.date.available | 2006-07-25 | |
dc.date.copyright | 2006-07-25 | |
dc.date.issued | 2006 | |
dc.date.submitted | 2006-07-21 | |
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dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33080 | - |
dc.description.abstract | 我們已經合成ㄧ系列含1,3,4-氧二氮呃之小分子與高分子的有機共軛發光材料,藉由引入旋環雙芴基,在光物理、熱性質及電化學方面均有不錯的表現,特別是多功能性的樹枝狀寡聚合物,同時帶有咔唑及1,3,4-氧二氮呃等基團,在核磁共振光譜上有一些有趣的現象;另外我們也合成出以旋環雙芴為中心,透過三苯胺及咔唑等強推電子基團與1,3,4-氧二氮呃強拉電子基團的加入之新型二極性材料,發現於電聚合實驗後所產生的薄膜態在不同氧化態的顏色變化特別顯著,而且具有高著色效率和高對比度並且可以應用在電致變色材料上。然而含1,3,4-氧二氮呃之高分子聚合物材料上,也透過bisphenol A的加入,改善了其溶解度和光學性質。除此之外,在二極性高分子聚合物的主鏈上以1,3,4-氧二氮呃當作電子傳遞材料,在主鏈上吊掛咔唑當作電洞傳遞材料,透過這樣的組合方式可以輕易的調整電子與電洞的比例,達到電荷傳輸的最佳狀態。 | zh_TW |
dc.description.abstract | We have synthesized a novel series of organic light emitting materials which contained 1,3,4-oxadiazole (OXD) in small molecules and polymers. We introduced 9,9’-spirobifluorene group into the structure to increase the efficiency in photophysics and thermal stability. Especially multifunctionalized dendrimers with carbazole (CBZ) and 1,3,4-oxadiazole exhibit some interesting phenomenons in the nuclear magnetic resonance spectrum. A novel 9,9’-spirobifluorene-cored donor-acceptor (D-A) bichromophore system has been synthesized, where the electron-donating (D) moieties are triphenylamine (TPA) groups and carbazole group, and the electron-withdrawing (A) moieties are 1,3,4-oxadiazole groups which can impede electronic interactions between the TPAs, consequently allow to undergo efficient electropolymerization processes. The polymer film obtained showed reversible electrochemical oxidation accompanied by strong color changes with high coloration efficiency and contrast ratio, which can be switched by potential modulation. In another direction, polymers based on 1,3,4-oxadiazole polymer and bisphenol A were synthesized and found to exhibit good solubility and optical properties. In addition, we prepared bipolar polymer with 1,3,4-oxadiazole as electron transporting material in the backbone with carbazole branching as the hole transporting units. The methodology developed can allow as to adjust the electron and hole proportion. | en |
dc.description.provenance | Made available in DSpace on 2021-06-13T04:24:15Z (GMT). No. of bitstreams: 1 ntu-95-D90223002-1.pdf: 5834353 bytes, checksum: 8887f00b2f9f3c5e51dfa9f67316935d (MD5) Previous issue date: 2006 | en |
dc.description.tableofcontents | 目錄 i
表目錄 iv 圖目錄 v 化合物編號索引 ix 中文摘要 xv 英文摘要 xviii 第一章 緒論 1 1-1 前言 1 1-2 有機發光二極體發展歷史 2 1-3 有機發光二極體元件構造與發光原理 6 1-3.1 元件構造 6 1-3.2 發光原理 10 1-4 電子傳導材料 (ETM) 11 1-5 電洞傳導材料 (HTM) 14 1-6 OLED與PLED之優缺點 18 第二章 多功能性樹枝狀含1,3,4-氧二氮呃之旋環雙芴寡聚合物之合成設計與性質探討 20 2-1 樹枝狀寡聚合物的設計 20 2-1.1 隔離者 (spacer)的選擇 20 2-1.2 咔唑及1,3,4-氧二氮呃基團的引入 21 2-2 樹枝狀寡聚合物之合成 23 2-3 樹枝狀寡聚合物之核磁共振光譜性質 29 2-4 樹枝狀寡聚合物之光物理性質 39 2-5 樹枝狀寡聚合物之熱性質 45 2-6 樹枝狀寡聚合物之電化學性質 50 第三章 含二苯胺與咔唑及1,3,4-氧二氮呃之Y字形旋環雙 芴寡聚合物的合成設計與性質探討 60 3-1 電致變色的簡介 60 3-2 電致變色的元件結構 64 3-3 Y字形寡聚合物的合成設計 66 3-4 Y字形寡聚合物的光物理性質 71 3-5 Y字形寡聚合物的熱性質 72 3-6 Y字形寡聚合物的電化學性質 74 第四章 含Bisphenol A及1,3,4-氧二氮呃的高分子聚合物之 合成設計與性質探討 83 4-1 高分子聚合物的設計與合成 83 4-2 高分子聚合物的光物理性質 92 4-3 高分子聚合物的熱性質 94 4-4 高分子聚合物的電化學性質 96 第五章 二極性高分子聚合物含咔唑及1,3,4-氧二氮呃之合 成設計與性質探討 97 5-1 高分子聚合物的設計 97 5-1.1 調配HT與ET的數目 97 5-1.2 二極性高分子聚合物的合成 100 第六章 含9,9’-旋環雙戊[d,e,f]雙菲的合成設計與性質 121 6-1 9,9’-旋環雙戊[d,e,f]雙菲之交叉共軛 (spiro-conjugation) 系統的設計與合成 121 第七章 結論 139 第八章 實驗部份 141 8-1 實驗儀器 141 8-2 實驗步驟 144 參考文獻 202 附錄化合物之1H 與13C NMR 光譜 214 | |
dc.language.iso | zh-TW | |
dc.title | 含1,3,4-氧二氮呃之有機發光材料之合成與性質 | zh_TW |
dc.title | Synthesis and Characteristics of Organic Light Emitting Materials Based on 1,3,4-Oxadiazole | en |
dc.type | Thesis | |
dc.date.schoolyear | 94-2 | |
dc.description.degree | 博士 | |
dc.contributor.coadvisor | 汪根欉 | |
dc.contributor.oralexamcommittee | 梁文傑,周大新,徐秀福 | |
dc.subject.keyword | 1,3,4-氧二氮呃,二極性之電致變色材料, | zh_TW |
dc.subject.keyword | 1,3,4,-oxadiazole,bipolar electrochromic material, | en |
dc.relation.page | 214 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2006-07-22 | |
dc.contributor.author-college | 理學院 | zh_TW |
dc.contributor.author-dept | 化學研究所 | zh_TW |
顯示於系所單位: | 化學系 |
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