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  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/123456789/22566
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DC 欄位值語言
dc.contributor.advisor邱勝賢(Sheng-Hsien Chiu)
dc.contributor.authorZu-Feng Linen
dc.contributor.author林祖鳳zh_TW
dc.date.accessioned2021-06-08T04:21:00Z-
dc.date.copyright2010-07-21
dc.date.issued2010
dc.date.submitted2010-07-16
dc.identifier.citation1. Lehn J. M. Supramolecular Chemistry, VCH: Weinhein, 1995.
2. Nicolaou, K.C.; Vourloumis, D.; Winssinger, N.; Baran, P.S. Angew. Chem. Int. Ed. Engl. 2000, 39, 44–122.
3. Atwood J. L.; Jonathan W. Steed Encyclopedia of Supramolecular Chemistry Marcel Dekker, Inc.: New York, 2004.
4. Muller-Dethlefs, K.; Hobza, P. Chem. Rev. 2000, 100, 143–167.
5. (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.
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. (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.
8. (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.
9. Atwood J. L. (Ed.), Inclusion Phenomena and Molecular Recognition, Plenum Press: New York, 1988.
10. Please refer to a special issue: Nature 2001, 413, 185–230.
11. (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.
12. (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.
13. Yoon, I.; Narita, M.; Shimizu, T.; Asakawa, M. J. Am. Chem. Soc. 2004, 126, 16740–16741.
14. Chiu, C.-W.; Lai, C.-C.; Chiu , S.-C. J. Am. Chem. Soc. 2007, 129, 3500–3501.
15. (a) Allwood, B. L.; Spencer, N.; Shahriari-Zavareh, H.; Stoddart, J. F.; Williams, D. J. J. Chem. Soc., Chem. Commun. 1987, 1058. (b) Asakawa, M.; Ashton, P. R.; Ballardini, R.; Balzani, V.; Belohradsky, M.; Gandolfi, M. T.; Kocian, O.; Prodi, L.; Raymo, F. M.; Stoddart, J. F.; Venturi, M. J. Am. Chem. Soc. 1997, 119, 302. (c) Asakawa, M.; Ashton, P. R.; Boyd, S. E.; Brown, C. L.; Gillard, R. E.; Kocian, O.; Raymo, F. M.; Stoddart, J. F.; Tolley, M. S.; White, A. J. P.; Williams, D. J. J. Org. Chem. 1997, 62, 26.
16. Bryant, W. S.; Jones, J. W.; Mason, P. E.; Guzei, I. A.; Rheingold, A. L.; Nagvekar, D. S.; Gibson, H. W. Org. Lett. 1999, 1, 1001–1004.
17. (a) Cram, D. J. Angew. Chem. Int. Ed. Engl. 1986, 25, 1039–1057. (b) Maverick, E.; Cram, D. J. Compr. Supramol. Chem. 1996, 213–243.
18. (a) Rao, J.; Lahiri, J.; Issacs, L.; Weis, R. M.; Whitesides, G. M. Science 1998, 280, 708–711. (b) Rao, J.; Yan, L.; Xu, B.; Whitesides, G. M. J. Am. Chem. Soc. 1999, 121, 2629–2630. (c) Mammen, M.; Chio, S.-K.; Whitesides, G. M. Angew. Chem. Int. Ed. 1998, 37, 2755–2794.
19. Cheng, P.-N.; Huang, P.-Y.; Li, W.-S.; Ueng, S.-H.; Hung, W.-C.; Liu, Y.-H.; Lai, C.-C.; Peng, S.-M.; Chao, I.; Chiu, S.-H. J. Org. Chem. 2006, 71, 2373−2375.
20. Cheng, P.-N.; Lin, C.-F.; Liu, Y.-H.; Lai, C.-C.; Peng, S.-M.; Chiu, S.-H. Org. Lett. 2006, 8, 435−438.
21. Robinson, G.M. J. Chem. Soc. Trans. 1915, 107, 267–276.
22. (a) Lindsey, A. S. Chem. Ind. (London) 1963, 824–824. (b) Lindsey, A. S. J. Chem. Soc. 1965, 1685–1692. (c) Erdtman, H.; Halglid, F.; Ryhage, R. Acta Chem. Scand. 1964, 18, 1249–1254. (d) Golduo, A.; Morrison, A. B.; Smith, G. W. J. Chem. Soc. 1965, 3864–3865.
23. Zimmermann, H.; Tolstoy, P.; Limbach, H.-H.; Poupko, R.; Luz, Z. J. Phys. Chem. B 2004, 108, 18772–18778.
24. (a) Ibragimov, B. T.; Makhkamov, K. K.; Beketov, K. M. J. Inclusion Phenom. Macrocyclic Chem., 1999, 35, 583. (b) Caira, M. R.; Jacobs, A.; Nassimbeni, L. R. Supramol. Chem. 2004, 16, 337.
25. Hardie, M. J.; Raston, C. L. Chem. Commun. 1999, 1153.
26. Holman, K. T.; Steed, J. W.; Atwood, J. L. Angew. Chem., Int.Ed. Engl. 1997, 36, 1736.
27. Jerry L. Atwood, J. Am. Chem. Soc. 1994, 10346–10347.
28. Kentaro Yamaguchi Org. Lett. 2001, 3, 1085–1087.
29. Michaele J. Hardie Angew. Chem. Int. Ed. 2005, 6395–6399.
30. Gabard, J.; Collet, A. J. Chem. Soc., Chem. Commun. 1981, 1137–1139.
31. Noncovalent molecular cages have been prepared; see: (a) Kim, M.; Gokel, G. W. J. Chem. Soc. Chem. Commun. 1987, 1686–1688; (b) Kerckhoffs, J. M. C.; Leeuwen, F. W. B. van; Spek, A. L.; Kooijman,K.; Crego-Calama, M. D.; Reinhoudt, N. Angew. Chem. 2003, 115, 5895–5900; Angew. Chem. Int. Ed. 2003, 42, 5717–5722; (c) Yoshizawa, M.; Miyagi, S.; Kawano, M.; Ishiguro, K.; Fujita, M. J. Am. Chem. Soc. 2004, 126, 9172–9173; cryptand-type host molecules may be considered as the simplest covalently linked molecular cages; see: (d) Nielsen, K. A.; Jeppesen, J. O.; Levillain, E.; Thorup, N.; Becher, J. Org. Lett. 2002, 4, 4189–4192; (e) Perkins, D. F.; Lindoy, L. F.; Meehan, G. V.; Turner, P. Chem. Commun. 2004, 152–153; (f) Bonizzoni, M.; Fabbrizzi, L.; Piovani, G.; Taglietti, A. Tetrahedron 2004, 60, 159–11162; cryptophanes, carcerands, and hemicarcerands may also be considered as covalently linked molecular cages; see: (g) Collet, A.; Dutasta, J.-P.; Lozach, B.; Canceil, J. Top. Curr. Chem. 1993, 165, 103–130; (h) Jasat, A.; Sherman, J. C. Chem. Rev. 1999, 99, 931–967; (i) Warmuth, R. Acc. Chem. Res. 2001, 34, 95–105.
32. (a) Nepogodiev, S. A.; Stoddart, J. F. Chem. Rev. 1998, 98, 1959. (b) Easton, C. J.; Lincoln, S. F. Modified Cyclodextrins. Scaffolds and Templates for Supramolecular Chemistry, Imperial College Press, London, 1999. (c) Harada, A. Acc. Chem. Res. 2001, 34, 456.
33. (a) Atwood, J. L.; Barnes, M. J.; Gardiner, M. G.; Raston, C. L. Chem. Commun. 1996, 1449. (b) Atwood, J. L.; Barnes, M. J.; Burkhalter, R. S.; Junk, P. C.; Steed, J. W.; Raston, C. L. J. Am. Chem. Soc. 1994, 10346. (c) Bond, A. M.; Miao, W.; Raston, C. L.; Ness, T. J.; Barnes, M. J.; Atwood, J. L. J. Phys. Chem. 2001 in press.(d) Matsubara, H.; Hasegawa, A.; Shiwaku, K.; Asano, K.; Takahashi, S.; Yamamoto, K. Chem. Lett. 1998, 923. (e) Matsubara, H.; Oguri, S.; Asano, K.; Yamamoto, K. Chem. Lett. 1999, 431.
34. (a) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 2495–2496. (b) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 7017–7036.
35. (a) Diederich, F. Cyclophanes, The Royal Society of Chemistry, Cambridge, 1991. (b) Gomez-Lopez, M.; Preece, J. A.; Stoddart, J. F. Nanotechnology 1996, 7, 183.
36. Lin, C.-F.; Liu, Y.-H.; Lai, C.-C.; Peng, S.-M.; Chiu, S.-H. Chem. Eur. J. 2006, 12, 4594–4599.
37. Lin, C.-F.; Liu, Y.-H.; Lai, C.-C.; Peng, S.-M.; Chiu, S.-H. Angew. Chem. Int. Ed. 2006, 45, 3176–3181.
38. Li, M.-J.; Lai ,C.-C.; Liu, Y.-H.; Penga, S.-M.; Chiu, S.-H. Chem. Commun. 2009, 5814–5816.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/22566-
dc.description.abstract利用以環三聚藜烴為單元之分子容器1為主體,我們成功地利用具雙吡啶陽離子的桿狀分子與分子容器中兩個24員環開口端的辨識作用,在溶液中合成其相對應的車輪烷。將桿狀分子上的辨識中心轉變為尺寸較大的芳香環時,桿狀分子與分子容器經由相同反應所製作的車輪烷分子則是以穿隧分子容器上的一個24員環及其對面的34員環開口端為主。因此,利用不同桿狀分子穿隧分子容器之不同面向的開口端可達到控制不同種類車輪烷分子合成的目的。zh_TW
dc.description.abstractThe formation of pseudorotaxane complexes between cyclotriveratrylene-based molecular container and bipyridinium cation allowed us to synthesize the corresponding [2]rotaxane, in which the guest component penetrated two adjacent 24C8-like openings. Using similar synthetic approach but more sizable aromatic cation as the recognition unit, the guest components in the resulting [2]rotaxane penetrated one 24C8-like opening and its opposite 34-membered ring of the interlocked molecular container. Therefore, two types of guest complexation modes for molecular container were confirmed and the formation of their corresponding rotaxanes was realized.en
dc.description.provenanceMade available in DSpace on 2021-06-08T04:21:00Z (GMT). No. of bitstreams: 1
ntu-99-R97223120-1.pdf: 4349952 bytes, checksum: d0a70647a46e989c515f9d7d749d9034 (MD5)
Previous issue date: 2010
en
dc.description.tableofcontents謝 誌.....................................................I
摘 要....................................................II
Abstract.................................................III
目 次....................................................IV
圖 目 錄................................................VI
流 程 目 錄..........................................VIII
壹、導 論.................................................1
1.1 前言..............................................1
1.2 內鎖型分子........................................3
1.2.1 內鎖型分子定義.............................3
1.2.2 車輪烷分子的合成策略.......................4
1.3 多電子芳香環與缺電子的巴拉刈衍生物之超分子系統....5
1.4 環三聚藜烴(cyclotriveratrylene, CTV)............8
1.4.1 環三聚藜烴簡介.............................8
1.4.2 環三聚藜烴衍生物之應用.....................9
貳、結果與討論............................................11
2.1 研究動機.........................................11
2.2 具環三聚藜烴之[2]車輪烷分子的設計................15
2.3 結果與討論.......................................16
2.3.1 以bipyridinium為辨識中心之[2]車輪烷分子...16
2.3.2 以diazapyrenium為辨識中心之[2]車輪烷分子..24
参、結 論................................................30
肆、實驗部分..............................................31
伍、參考文獻..............................................42
dc.language.isozh-TW
dc.title以具CTV單元之分子容器製作車輪烷分子的研究zh_TW
dc.titleToward the Synthesis of CTV-Based [2]Rotaxanesen
dc.typeThesis
dc.date.schoolyear98-2
dc.description.degree碩士
dc.contributor.oralexamcommittee徐秀福,賴建成
dc.subject.keyword車輪烷,分子容器,zh_TW
dc.subject.keywordrotaxane,molecular container,en
dc.relation.page46
dc.rights.note未授權
dc.date.accepted2010-07-16
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
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