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  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 化學系
Please use this identifier to cite or link to this item: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28476
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???org.dspace.app.webui.jsptag.ItemTag.dcfield???ValueLanguage
dc.contributor.advisor梁文傑
dc.contributor.authorMeng-Lin Tsaien
dc.contributor.author蔡孟林zh_TW
dc.date.accessioned2021-06-13T00:09:23Z-
dc.date.available2008-03-31
dc.date.copyright2007-07-31
dc.date.issued2007
dc.date.submitted2007-07-27
dc.identifier.citation(1) De Silva, A. P.; Gunaratne, H. Q. N.; Gunnlaugsson, T.; Huxley, A. J. M.;McCoy,
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(14)周孟彥,以2,2’-雙取代聯苯為核心之三苯基胺衍生物的合成,價間電子轉移
研究及有機光電元件的應用,國立台灣大學博士論文,民國九十二年。
(15)趙君傑,含苝環之小分子與高分子之合成、性質探討及其太陽能電池上的應
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民國九十五年。
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dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/28476-
dc.description.abstract我們成功合成出聯苯二醯亞胺這種具有雙極性特性的分子。藉由分子結構的限制,使聯苯間的共軛性質變好,使分子內能有效的產生光致電荷轉移。藉由取代基效應觀察化合物光物理性質及電化學特性的改變。接著利用化合物電荷轉移的特性和醇類產生氫鍵作用力淬息螢光;由電化學的討論我們得知,分子結構(聯苯的雙面角)對電化學有很大的影響。當雙面角小於某一個角度,聯苯間的電子能夠有效的共振,電聚合就不會產生;反之,當聯苯雙面角過大,聯苯間電子無法共振,就會有電聚合情形的發生。zh_TW
dc.description.abstractWe succeed synthesize dipolar biphenyl diimide derivatives. Intramolecular photoinduced charge transfer can be efficiency by restricting biphenyl group to make it more conjugate. We observe photophysical and electrochemistry property of biphenyl imide by substitutent group effect. The charge transfer property of biphenyl diimide induce hydrogen bond formation with alcohol to quench fluorescence; Discusses us by the electrochemistry to know that, the molecular structure (dihedral angle of biphenyl group) have the very heavy influence to the electrochemistry. When the dihedral angle is small enough, the electron can be more efficiency resonance on biphenyl group, and the electropolymerization don’t occur. Contrary, when the dihedral angle is big enough, the compound can be electronpolymerization.en
dc.description.provenanceMade available in DSpace on 2021-06-13T00:09:23Z (GMT). No. of bitstreams: 1
ntu-96-R94223026-1.pdf: 2596149 bytes, checksum: a9dc3ee31940f68c9556c9afc5807d5c (MD5)
Previous issue date: 2007
en
dc.description.tableofcontents目錄
目錄……………………………………………………………...................................I
圖目錄……………………………………………………………...............................II
表目錄…………………………………………………………………….……..……V
化合物結構與編號……………………………………….……..…………………...VI
摘要…………………………………………………………………………………..IX
Abstract……………………………………………………………………………….X
第一章 緒論………………………………………………………….……………..1
第一節 有機分子之螢光特性初論……………………..…………..………..1
第二節 分子內電荷轉移………………………………………………….….2
第三節 ICT光物理性質…………………………………………….……..…3
第四節 三苯胺基化合物……………………………………………….…….5
第五節 聯苯二醯亞胺設計概念………………………………………….….7
第二章 聯苯二醯亞胺合成策略與方法……………………………………...……8
第一節 聯苯二醯亞胺分子結構設計………………………………..……....8
第二節 化合物的合成………………………………………………..……....8
第三節 聯苯二醯亞胺結構探討…………………………………………....13
第四節 聯苯二醯亞胺的光學性質探討…………………………………..15
第五節 溶劑極性對雙極性分子的影響…………………………………....24
第六節 分子間氫鍵作用力淬息螢光……………………………………....34
第七節 聯苯二醯亞胺電化學特性探討…………………….……………...47
第八節 聯苯二醯亞胺電聚合化學行為探討………………………….…...57
第三章 結論………………………………………………………………….……64
第四章 參考文獻………………………………………………………….……....65
第五章 實驗部份…………………………………………………………….……67
附錄I 化合物之1H與13C核磁共振光譜圖……………………………………..85
附錄II 化合物X-ray晶體參數表、鍵長及鍵角資料……………………….……134
dc.language.isozh-TW
dc.subject聯苯zh_TW
dc.subject雙極性分子zh_TW
dc.subject光化學zh_TW
dc.subject淬息螢光zh_TW
dc.subject氫鍵zh_TW
dc.subjectdipolar molecularen
dc.subjectbiphenyl groupen
dc.subjecthydrogen bonden
dc.subjectquench fluorescenceen
dc.subjectphotochemistryen
dc.title3,9-雙-二苯胺-二苯並[c,e]氮雜環-5,7-二酮及其衍生物之合成與光性質研究zh_TW
dc.titleSynthesis and Photophysical Studies of 3,9-Bis-diphenylamino-dibenzo[c,e]azepine-5,7-dione
Derivatives
en
dc.typeThesis
dc.date.schoolyear95-2
dc.description.degree碩士
dc.contributor.oralexamcommittee林萬寅,徐秀福
dc.subject.keyword雙極性分子,光化學,淬息螢光,氫鍵,聯苯,zh_TW
dc.subject.keyworddipolar molecular,photochemistry,quench fluorescence,hydrogen bond,biphenyl group,en
dc.relation.page66
dc.rights.note有償授權
dc.date.accepted2007-07-30
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
Appears in Collections:化學系

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