Skip navigation

DSpace

機構典藏 DSpace 系統致力於保存各式數位資料(如:文字、圖片、PDF)並使其易於取用。

點此認識 DSpace
DSpace logo
English
中文
  • 瀏覽論文
    • 校院系所
    • 出版年
    • 作者
    • 標題
    • 關鍵字
  • 搜尋 TDR
  • 授權 Q&A
    • 我的頁面
    • 接受 E-mail 通知
    • 編輯個人資料
  1. NTU Theses and Dissertations Repository
  2. 理學院
  3. 化學系
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/9763
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor楊吉水(Jye-Shane Yang)
dc.contributor.authorKa-Shu Fungen
dc.contributor.author馮嘉樹zh_TW
dc.date.accessioned2021-05-20T20:39:55Z-
dc.date.available2011-07-30
dc.date.available2021-05-20T20:39:55Z-
dc.date.copyright2008-07-30
dc.date.issued2008
dc.date.submitted2008-07-23
dc.identifier.citation( 1 ) Zaumseil, J.; Sirringhaus, H.; Chem. Rev. 2007, 107, 1296-1323
( 2 ) Kraft, A.; Grimsdale, A. C.; Holmes A. B.; Angew. Chem. Int. Ed. 1998, 37, 402-428
( 3 ) Günes, S.; Neugebauer, H.; Sariciftci, N. S.; Chem. Rev. 2007, 107, 1324-1338
( 4 ) McQuade, D. T.; Pullen, A. E.; Swager, T. M.; Chem. Rev. 2000, 100, 2537-2574
Thomas, S. W.; Joly, G. D.; Swager, T. M.; Chem. Rev. 2007, 107, 1339-1386
( 5 ) Burroughes, J.; Bradley, D.; Brown, A.; Marks, R.; Mackay, K.; Eriend, R.; Burn, P.; Holmes, A.; Nature. 1990, 347,539
( 6 ) Brédas, J. L.; Beljonne, D.; Coropceanu, V.; Conil, J.; Chem. Rev. 2004, 104, 4971-5003
( 7 ) Heeger, A. J.; Braun, D.; WO-B; Chen.Abstr. 1993, 118, 157401j
( 8 ) Qibing, P.; Yang, Y.; J. Ac. Soc. Chem. 1996, 118, 7416-7417
( 9 ) Tang, R.; Tan, Z.; Li, Y.; Xi,.F.; Chem. Mater.. 2006 18, 1053-1061
( 10 ) Lee, Y-Z. ;Chen, X.; Chen, S-A.;Wei, P-K.; Fann, W-S.; J. Ac. Soc. Chem. 2001, 123, 2296-2307
( 11 ) Greenham, N. C.; Cacialli, F.; Bradley, D. D. C.; Friend, R. H.; Holmes, A. B.; Nature. 1993, 365, 628-630
( 12 ) Ahn, T.; Ko, S-W.; Lee, J.; Shim, H-K.; Macromolecules, 2002, 35, 3495-3505
( 13 ) Geffroy, B.; Roy, P.; Prat, C.; Polym. Int. 2006, 55, 572-582
( 14 ) Berggren, M.; Inganäs. O.; Gustafsson, G.; Rasmusson, J.; Andersson, M. R.; Hjertberg, T.; Wennerström, O.; Nature. 1994, 372, 444
( 15 ) Chuang, C.-Y.; Shih, P.-I.; Chien, C.-H.; Wu F.-L.; Shu, C.-F. Macromolecules, 2007, 40, 247-252
( 16 ) Amrutha, S. R.; Jayakannan, M.; Macromolecules 2007, 40, 2380-2391
( 17 ) Horhant, D.; Liang, J-J,; Virboul, M.; Poriel, C.; Alcaraz, G.; Berthelot, J. R.; Org. Lett. 2006, 8, 257-260
( 18 ) Kimura, M.; Sato, M.; Adacchi, N.; Fukawa, T.; Kanbe, E.; Shirai, H.; Chem. Mater. 2007, 19, 2809-2815
( 19 ) Sariciftci, N. S.; Smilowitz, L.; Hegger, A. J.; Science, 1992, 258, 1474-1476
( 20 ) Kim, J.; McQuade, D. T.; McHugh, S. K.; Swager, T. M.; Angew. Chem., Int. Ed. 2000, 39, 3868
( 21 ) Marsella, M. J.; Swager, T. M.; J. Am. Chem. Soc. 1993, 115,12214-12215
Wang, B.; Wasielewski, M. R.; J. Am. Chem. Soc. 1997, 119, 12-21.
Liu, B.; Yu, W.-L.; Pei, J.; Liu, S.-Y.; Lai, Y.-H.; Huang, W.; Macromolecules 2001, 34, 7932.
( 22 ) Veen, E. M.; Postma, P. M.; Jonkman, H. T.; Spek A. L. and Fering, B.L. Chem. Commun., 1999, 1709
( 23 )Yang J.-S.; Lin C.-S. and Hwang C.-Y.; Org. Lett. 2001, 3, 889-892
( 24 )Yang, J.-S.; Lee, C.-C.; Yau, S.-L.; Chang, C.-C.; Lee, C.-C.; Leu, J.-M.; J. Org. Chem. 2000, 65, 871
( 25 )Thomas, S. W., III; Long, T. M.; Pate, B. D.; Kline, S. R.; Thomas, E. L.; Swager, T. M.; J. Am. Chem. Soc, 2005; 127, 17976-17977
( 26 )Tsui, N .T.; Torun, L.; Paraskos, A. J.; Swager, T. M.; thomas, E. L.;Macromolecules, 2006, 39, 3350
( 27 )Yang J.-S.; Huang, Y.-T.; Ho, J.-H.; Sun, W.-T.; Huang, H.-H.; Lin, Y.-C.; Huang, S.-J.; Huang, S.-L.; Lu, H.-F.; Chao, I. Org. Lett, 2008, 10, 2279-2282
( 28 )Yang, J.-S.; Swager, T. M .; J. Am. Chem. Soc., 1998, 120, 11864-11873
( 29 )Kim, Y.; Whitten, J. M.; Swager, T. M .; J. Am. Chem. Soc., 2005, 127, 12122-12130
( 30 )S. W. Thomas III, T. M. Swager, Adv. Mater., 2006, 18,1047
( 31 )Zhu, Z.; Swager, T. M .; J. Am. Chem. Soc., 2002, 124, 9670-9671
( 32 )Nesterov, E. E.; Zhu, Z.; Swager, T. M .; J. Am. Chem. Soc., 2005, 127, 10083-10088
( 33 )Amara J. P.; Swager, T. M .; Macromolecule., 2006, 39, 5753-5759
( 34 )Breen, A. A.; Rifai, S.; Bulovic, V.; Swager, T. M.; Nano Lett., 2005, 5, 1591-1601
( 35 )柯青煒,五苯荑醌之官能化反應與新型五苯荑衍生物之合成,國立中央大學碩士論文,2006,1-22
( 36 )Yang, J.-S;. Ko, C.-W.; J.Org. Chem. , 2006, 71, 844-847
( 37 )Doyle, M. P.; Van Lente, M. A.; Mowat, R.; Fobare W. F.; J.Org. Chem. 1980, 45, 2570-2575
( 38 )Elangovan, E.; Wang, Y-H.; Ho, T-I.; Org. Lett. 2003, 5, 1841-1844
( 39 ) Bao, Z.; Chen, Y.; Cai, R.; Yu, L.; Macromoleculea, 1993, 26, 5281-5286
( 40 ) Zhu, Z.; Swager, T. M.; Org. Lett., 2001, 3, 3471-3474
( 41 ) Pang, Y. ; Li, J.; Macromoleculea, 1999, 32, 3946-3950
( 42 ) Morisaki, Y.; Ishida, T.; Chujo, Y.; Macromoleculea, 2002, 35, 7872-7877
( 43 )Tirapattur, S.; Belletête, M.; Drolet, N.; Bouchard, J.; Ranger, M.; Leclerc, M.; Durocher, G.; J. Phys. Chem. B., 2002, 106, 8959-8966
( 44 ) Ranger, M.; Rondeau, D.; Leclerc, M.; Macromoleculea, 1997, 30, 7872-7877
( 45 ) Morisaki, Y.; Ishida, T.; Chujo, Y.; Macromoleculea, 2002, 35, 7872-7877
( 46 )Yang, J.-S.; Yan, J.-L.; Hwang, C.-Y.; Chiou, S.-Y.; Liau, K.-L.; Tsai H.-H. G.; Lee, G.-H.; Peng, S.-M.; J. Am. Chem. Soc., 2006, 128, 14109-14119
( 47 ) Kim, Y.; Zhu, Z.; Swager, T. M.; J. Am. Chem. Soc., 2004, 126, 452-453
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/9763-
dc.description.abstract五苯荑分子乃是由兩個雙環[2.2.2]辛烷作為架橋把五個苯環相連而成的分子,其巨大且剛硬的三維結構與分子內自由空間,於共軛高分子中有著特殊的運用。由於缺乏合適的五苯荑單體,目前的相關研究皆偏重於聚苯乙炔系統。經由多年的開發,我們實驗室成功合成出中央苯環具有兩個溴的雙溴五苯荑,利用不同的有機金屬偶合反應,可以合成出各式各樣的共軛高分子系統。本論文的工作主要為嘗試改善雙溴五苯荑的合成,並合成於主鏈中含有五苯荑結構的聚苯乙烯、聚茀及全為五苯荑的聚苯乙炔。相對於常見的聚苯乙烯及聚茀,導入五苯荑結構後的共軛高分子之最大吸收與螢光波長皆有50 nm左右的藍位移現象;而全為五苯荑的聚苯乙炔由於幫助溶解的長碳鏈以hyperconjugation的方式和主鏈溝通,造成分子內電荷轉移的現象。zh_TW
dc.description.abstractPentiptycene, a molecule with five benzene rings fused together through two bicyclo[2,2,2,]octane moieties, is a interesting building block in materials chemistry because of its rigid three dimensional structure as well as internal free volume. In past, pentiptycene-derived conjugated polymers are limited to poly(phenyleneethynylene) (PPE) systems because of the absence of suitable building blocks for making different polymer backbones. After years of searching, we have successfully synthesized dibromopentiptycene, which allows use to prepare a variety of pentitpycene-incoporated conjugated polymers, including poly(phenylenevinylene) (PPV), polyfluorene (PF) and all-pentiptycene PPE by using different kinds of organometallic coupling reactions. Compared to common PPVs and PFs, the pentitpycene-incoporated PEN-PPV and PEN-PF undergo blue shifts by about 50 nm in both absorption and fluorescence spectra. The all-pentiptycene PEN-PPE shows intramolecular charge transfer character, presumably due to the dialkoxy substituted phenylene rings functioning as electron donors through hyperconjugation interactions.en
dc.description.provenanceMade available in DSpace on 2021-05-20T20:39:55Z (GMT). No. of bitstreams: 1
ntu-97-R95223046-1.pdf: 4400987 bytes, checksum: e552750faa2c055dc1dd574d0b266c94 (MD5)
Previous issue date: 2008
en
dc.description.tableofcontents口試委員審定書
謝誌
中文摘要
英文摘要
第一章 前言................................................1
1-1 共軛高分子之介紹...................................1
1-1-1 共軛高分子之發展.............................1
1-1-2 有機場效電晶體...............................3
1-1-3 有機發光二極體...............................3
1-1-4 有機太陽能電池...............................6
1-1-5 化學感應器...................................7
1-1-6 共軛高分子之特徵與效能.......................8
1-2 苯荑之化學.........................................9
1-2-1 苯荑類分子之結構.............................9
1-2-2 苯荑結構之運用...............................9
1-2-3苯荑於共軛高分子之運用.......................13
1-2-4 五苯荑的合成................................16
1-3 研究動機..........................................19
第二章 結果與討論.........................................20
2-1 化合物的合成......................................20
2-1-1 雙溴五苯荑之合成............................20
2-1-2 PEN-PPV單體(化合物16)的合成.................24
2-1-3 PEN-PF 單體(化合物19)的合成.................26
2-1-4 PEN-PPE單體(化合物26)的合成.................27
2-1-5 三氟甲磺酸酯基之還原........................31
2-1-6 有機金屬催化聚合反應........................34
2-2 光學性質探討......................................36
2-2-1 PEN-PPV之光學性質探討.......................36
2-2-2 PEN-PF 之光學性質探討.......................40
2-2-3 PEN-PPE 之光學性質探討......................43
第三章 結論...............................................47
第四章 實驗部分...........................................48
4-1 實驗藥品與溶劑....................................48
4-2 實驗儀器與方法....................................54
4-3 實驗步驟..........................................57
參考資料..................................................70
dc.language.isozh-TW
dc.title五苯荑衍生之共軛高分子之合成與性質研究zh_TW
dc.titleSynthesis and Properties of Pentiptycene Derived Conjugated Polymeren
dc.typeThesis
dc.date.schoolyear96-2
dc.description.degree碩士
dc.contributor.oralexamcommittee蔡蘊明(Yeun-Min Tsai),周大新(Tah-Sin Chow)
dc.subject.keyword五苯荑,共軛高分子,zh_TW
dc.subject.keywordPentiptycene,Conjugated Polymer,en
dc.relation.page71
dc.rights.note同意授權(全球公開)
dc.date.accepted2008-07-25
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

文件中的檔案:
檔案 大小格式 
ntu-97-1.pdf4.3 MBAdobe PDF檢視/開啟
顯示文件簡單紀錄


系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。

社群連結
聯絡資訊
10617臺北市大安區羅斯福路四段1號
No.1 Sec.4, Roosevelt Rd., Taipei, Taiwan, R.O.C. 106
Tel: (02)33662353
Email: ntuetds@ntu.edu.tw
意見箱
相關連結
館藏目錄
國內圖書館整合查詢 MetaCat
臺大學術典藏 NTU Scholars
臺大圖書館數位典藏館
本站聲明
© NTU Library All Rights Reserved