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
    • 指導教授
  • 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/123456789/40865
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor蔡蘊明
dc.contributor.authorTzu-Chiun Linen
dc.contributor.author林子群zh_TW
dc.date.accessioned2021-06-14T17:04:07Z-
dc.date.available2013-08-05
dc.date.copyright2008-08-05
dc.date.issued2008
dc.date.submitted2008-07-29
dc.identifier.citation1.(a) Nicolaou, K. C.; Vourloumis, D.; Winssinger, N.; Baran, P. S. Angew. Chem. Int. Ed. 2000, 39, 44–122.
2.Muller-Dethlefs, K.; Hobza, P. Chem. Rev. 2000, 100, 143–167.
3.(a) Ghadiri, M. R.; Granja, J. R.; Milligan, R. A.; McRee, D. E.; Khazanovich, N. Nature 1993, 366, 324–327. (b) Whitesides, G. M.; Simanek, E. E.; Mathias, J. P.; Seto, C. T.; Chin, D. N.; Mammen, M.; Gordon, D. M. Acc. Chem. Res. 1995, 28, 37–44. (c) Zimmerman, S. C.; Zeng, F.; Reichert, D. E. C.; Kolotuchin, S. V. Science 1996, 271, 1095–1098. (d) Mascal, M.; Hext, N. M.; Warmuth, R.; Moore, M. H.; Turkenburg, J. P. Angew. Chem. Int. Ed. 1996, 35, 2204–2206. (e) Sijbesma, R. P.; Beijer, F. H.; Brunsveld, L.; Folmer, B. J. B.; Hirschberg, J. H. K. K.; Lange, R. F. M.; Lowe, J. K. L.; Meijer, E. W. Science 1997, 278, 1601–1604. (f) Rebek, J., Jr. Acc. Chem. Res. 1999, 32, 278–286.
4.(a) Dougherty, D. A. Science 1996, 271, 163–168. (b) Ma, J. C.; Dougherty, D. A. Chem. Rev. 1997, 97, 1303–1324. (c) Gokel. G. W.; De Wall, S. L.; Meadows, E. S. Eur. J. Org. Chem. 2000, 17, 2967–2978. (d) Gokel, G. W.; Barbour, L. J.; Ferdani, R.; Hu, J. Acc. Chem. Res. 2002, 35, 878–886.
5.(a) Chambron, J.-C.; Chardon-Noblat, S.; Dietrich-Buchecker, C. O.; Heitz, V.; Sauvage, J.-P. Macrocycle Synthesis 1996, 207–246. (b) Fujita, M.; Umemoto, K.; Yoshizawa, M.; Fujita, N.; Kusukawa, T.; Biradha, K. Chem. Commun. 2001, 509–518. (c) Kim, K. Chem. Soc. Rev. 2002, 31, 96–107.
6.(a) Hunter, C. A.; Sanders, J. K. M. J. Am. Chem. Soc. 1990, 112, 5525–5534. (b) Philip, D.; Slawin, A. M. Z.; Spencer, N.; Stoddart, J. F.; Williams, D. J. J. Chem. Soc. Chem. Commun. 1991, 1584–1586. (c) Hamilton, D. G.; Davies, J. E.; Prodi, L.; Sanders, J. K. M. Chem. Eur. J. 1998, 4, 608–620.
7.Lehn J.-M. Supramolecular Chemistry, VCH: Weinhein, 1995.
8.Muller-Dethles, K.; Hobza, P. Chem. Rev. 2000, 100, 143–167.
9.(a) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 2495–2496. (b) Gokel, G. W. Crown Ethers and Cryptands, Royal Society of Chemistry: London, 1991 (c) Diedrich, F. N. Cyclophanes, Royal Society of Chemistry: London, 1991 (d) Gutsche, C. D. Calixarenes, Royal Society of Chemistry: London, 1989 (e) Vogtle F.; Weber E. (Eds), Host Guest Complex Chemistry: Macrocycles Springer: New York, 1985 (f) Cram, D. J.; Cram, J. M. Container Molecules and Their Guests, Royal Society of Chemistry: London, 1994.
10.Atwood J. L. (Ed.), Inclusion Phenomena and Molecular Recognition, Plenum Press: New York, 1988.
11.Breault, G. A.; Hunter C. A.; Mayers P. C. Tetrahedron, 1999, 55, 5265–5293
12.Corbett P. T., West, K. R., Wietor J.-L., Sanders K. M., Sijbren Otto. Chem. Rev. 2006, 106, 3652 – 3711.
13.Please refer to a special issue: Nature 2001, 413, 185–230.
14.(a) Whitesides G. M.; Mathias, J. P.; Seto, C. T. Science 1991, 254, 1312–1319. (b) Lindoy, L. F.; Atkinson, I. M. Self-assembly in Supramolecular Systems, Royal Society of Chemistry: Cambridge, 2000. (c) Whitesides, G. M.; Grzybowski, B. Science 2002, 295, 2418–2421. (d) Boncheva, M.; Bruzewicz, D. A.; Whitesides, G. M. Pure Appl. Chem. 2003, 75, 621–630.
15.(a) Lehn, J.-M. Angew. Chem. Int. Ed. Engl. 1988, 27, 89–112. (b) Cram, D. J. Angew. Chem. Int. Ed. Engl. 1988, 27, 1009–1020. (c) Pedersen, C. J. Angew. Chem. Int. Ed. Engl. 1988, 27, 1021–1027.
16.(a) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 2495–2496. (b) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 7017–7036.
17.Steed, J-. W. “Supramolecular Chemistry”; John Wiley, 2002.
18.Cram, D. J.; Helgeson, T. K. R. C.; Lein, G. M. J. Am. Chem. Soc. 1979, 101, 6752–6754.
19.Cram, D. J. Angew. Chem. 1986, 98, 1041–1060; Angew. Chem. Int. Ed. Engl. 1986, 25, 1039–1057.
20.(a) Jager, R.; Vogtle, F. Angew. Chem., Int. Ed. Engl. 1997, 36, 930-944. (b) Nepogodiev, S. A.; Stoddart, J. F. Chem. Rev. 1998, 98, 1959-1976. (c) Brouwer, A. M.; Fazio, S. M.; Frochot, C.; Gatti, F. G.; Leigh, D. A.; Wong, J. K. Y.; Wurpel, G. W. H. Pure Appl. Chem. 2003, 75, 1055-1060. (d) Chambron, J.-C.; Collin, J.-P.; Heitz, V.; Jouvenot, D.; Kern, J.-M.; Mobian, P.; Pomeranc, D.; Sauvage, J.-P. Eur. J. Org. Chem. 2004, 8, 1627-1638. (e) Kihara, N.; Hashimoto, M.; Takata, T. Org. Lett. 2004, 6, 1693-1696.
21.Amabilino, D. B.; Fraser Stoddart, J. F. Chem. Rev. 1995, 95, 2725-2828
22.Wasserman, E. J. Am. Chem. Soc. 1960, 82, 4433.
23.Harrison, I. T.; Harrison, S. J. Am. Chem. Soc. 1967, 89, 5723.
24.(a) Hubin, T. J.; Kolchinski, A. G.; Vance, A. L.; Busch, D. H. Template Control of Supramolecular Architectures. In Advances in Supramolecular Chemistry; Board 5, Series 237; JAI Press: 1999. (b) Diederich, F.; Stang, P. J. Template Directed Synthesis; Wiley- VCH: Weinheim, 2000.
25.Ching-Wei Chiu, Chien-Chen Lai, Sheng-Hsien Chiu, J. Am. Chem. Soc. 2007, 129, 3500-3501.
26.Badjic, J. D.; Nelson, A.; Cantrill, S. J.; Turnbull, W. B.; Stoddart, J. F. Acc. Chem. Res. 2005, 38, 723-732.
27.Ashton, P. R.; Stoddart, J. F.; J. Am. Chem. Soc. 1998, 120, 11932-11942.
28.Blazani, V.; Credi, A.; Mattertsteig, G.; Matthews, O. A.; Raymo, F. M.; Stoddart, J. F.; J. Org. Chem. 2000, 65, 1924-1936.
29.Ashton, P. R.; Ballardini, R.; Balzani, V.; Constable. E. C.; Credi, A.; Kocian, O.; Langford, S. J.; Preece, J. A.; Prodi, L.; Schofield, E. R.; Spencer, N.; Stoddart, J. F.; Wenger, S.; Chem. Eur. J. 1998, 4, 2412-2422.
30.Beer, P. D.; Gale, P. A. Angew. Chem. 2001, 113, 502-532; Angew. Chem. Int. Ed. 2001, 40, 486−516.
31. (a) Collin, J.-P.; Dietrich-Buchecker, C.; Gavina, P.; Jimenez-Molero, M. C.; Sauvage, J.-P. Acc. Chem. Res. 2001, 34, 477−487. (b) Kaiser, G.; Jarrosson, T.; Otto, S.; Ng, Y.-F.; Bond, A. D.; Sanders, J. K. M. Angew. Chem. 2004, 116,1993–1996; Angew. Chem. Int. Ed. 2004, 43, 1959−1962. c) Iijima, T.; Vignon, S. A.; Tseng, H.-R.; Jarrosson, T.; Sanders, J. K. M.; Marchioni, F.; Venturi, M.; Apostoli, E.; Balzani, V.; Stoddart, J. F. Chem. Eur. J. 2004, 10, 6375–6392. d) Badjic, J. D.; Balzani, V.; Credi, A.; Silvi, S.; Stoddart, J. F. Science 2004, 303, 1845–1849.
32. Keaveney, C. M.; Leigh, D. A. Angew. Chem. 2004, 116, 1242–1244; Angew. Chem. Int. Ed. 2004, 43, 1222–1224.
33. Laursen, B. W.; Nygaard, S.; Jeppesen, J. O.; Stoddart, J. F. Org. Lett. 2004, 6, 4167–4170.
34. Lin, C.-F.; Lai, C.-C.; Liu, Y.-H.; Peng, S.-M.; Chiu, S.-H. Chem. Eur. J. 2007, 13, 4350–4355.
35. Huang, Y.-L, Hung W.-C., Lai C.-C., Liu Y.-H., Peng S.-M., Chiu, S.-H. Angew. Chem. Int. Ed. 2007, 46, 6629–6633.
36. Cooper, M.D., M.P.H., Kenneth H., Advanced Nutritional Therapies, 1996, 87-88
37. Schmidtchen, F. P.; Berger, M. Chem. Rev. 1997, 97, 1609-1646.
38. Cheng, P.-N.; Huang, P.-Y.; Li, W.-S.; Ueng, S.-H.; Huang, W.-C.; Liu, Y.-H.; Lai C.-C.; Peng, S.-M.; Chao, I.; Chiu, S.-H. J. Org. Chem. 2006, 71, 2373–2375.
39. Cheng, P.-N.; Lin, C.-F.; Liu, Y.-H.; Lai, C.-C.; Peng, S.-M.; Chiu, S.-H. Org. Lett. 2006, 8, 435–438.
40. Linton, B. R., Carr, A. J., Orner, B. P., Hamilton, A. D. J. Org. Chem. 2000, 65, 1566.
41. Connors, K. A.; Binding Constants; Wiley: New York, 1987
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/40865-
dc.description.abstract我們合成了一個含有胍基(Guanidinium)的客體分子,並發現其可與適當的大環分子在低極性溶液中形成穩定的錯合物。為證明此一錯合物主要是以準車輪烷形式存在溶液中,我們以「穿透後封鎖法」合成出一個同時具有胍基和吡啶(Pyridinium)二個辨識中心的車輪烷分子並成功地藉著改變溶劑極性及加入/移除鹵素離子或醋酸根離子來加以控制大環分子和胍基分子間的錯合與解離,進而操作分子開關的移動異構化(translational isomerization)。zh_TW
dc.description.abstractWe have demonstrated that guanidinium ions can thread through the cavity of BPX26C6 to form [2]pseudorotaxane-like complexes in low-polarity solvents. A [2]rotaxane derived from this new recognition system functions as a molecular switch, in which translational movement of macrocyclic component can be controlled two ways: through changes in solovent polarity and through exchanges of the counter anions.en
dc.description.provenanceMade available in DSpace on 2021-06-14T17:04:07Z (GMT). No. of bitstreams: 1
ntu-97-R95223045-1.pdf: 1771597 bytes, checksum: 4fb1f891aff3330223cf2a04b05c86ce (MD5)
Previous issue date: 2008
en
dc.description.tableofcontents摘要 ... I
目次 ... III
式子 ... IV
圖表 ... V
流程 ... VII
表 格... VIII
壹、導論 ... 1
1.1 前言 ... 1
1.2 超分子化學 ... 2
1.3 內鎖型分子—車輪烷及環連體 ... 7
1.4 分子開關 ...11
1.5 以陰離子控制之分子開關.... 15
貳、結果與討論 ... 20
2.1 研究動機 ... 20
2.2 車輪烷分子的設計與合成...21
2.3 分子開關的改良與研究 ... 30
參、結論 ...40
肆、實驗部份 ...41
伍、參考文獻 ...60
附錄 2D-NMR、1H-NMR與 13C-NMR 核磁共振光譜 ...65
dc.language.isozh-TW
dc.subject陰離子zh_TW
dc.subject分子開關zh_TW
dc.subjectanionen
dc.subjectMolecular switchen
dc.title以胍基為基礎的分子開關之合成研究zh_TW
dc.titleA Guanidinium Ion-Based Anion Controllable Molecular Switchen
dc.typeThesis
dc.date.schoolyear96-2
dc.description.degree碩士
dc.contributor.coadvisor邱勝賢
dc.contributor.oralexamcommittee徐秀福,賴建成
dc.subject.keyword分子開關,陰離子,zh_TW
dc.subject.keywordMolecular switch,anion,en
dc.relation.page65
dc.rights.note有償授權
dc.date.accepted2008-07-29
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.pdf
  未授權公開取用
1.73 MBAdobe PDF
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