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完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.advisor | 邱勝賢(Sheng-Hsien Chiu) | |
dc.contributor.author | Han-Chen Xu | en |
dc.contributor.author | 徐涵辰 | zh_TW |
dc.date.accessioned | 2021-07-11T14:34:57Z | - |
dc.date.available | 2028-07-13 | |
dc.date.copyright | 2018-07-18 | |
dc.date.issued | 2018 | |
dc.date.submitted | 2018-07-13 | |
dc.identifier.citation | 1. Lehn, J. M. Science 1993, 260, 1762–1763.
2. Müller-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. Engl. 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. 4. (a) Neusser, H. J.; Krause, H. Chem. Rev. 1994, 94, 1829–1843; (b) Desfrançois, C.; Carles, S.; Schermann, J. P. Chem. Rev. 2000, 100, 3943–3962. 5. (a) Hunter, C. A.; Sanders, J. K. M. J. Am. Chem. Soc. 1990, 112, 5525–5534; (b) Philp, 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. 6. (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, 1967–1978; (d) Gokel, G. W.; Barbour, L. J.; Ferdani, R.; Hu, J. J. Acc. Chem. Res. 2002, 35, 878–886. 7. (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. 8. Naray-Szabo, G.; Ferenczy, G. G. Chem. Rev. 1995, 95, 829–847. 9. (a) Pratt, L. R.; Chandler, D. Chem. Phys. 1977, 67, 3683–3704; (b) Chandler, D. Nature 2005, 437, 640–647. 10. (a) Gokel, G. W. Crown Ethers and Cryptands, Royal Society of Chemistry: London, 1991; (b) Vögtle, F.; Weber, E. (Eds), Host Guest Complex Chemistry: macrocycles Springer: New York, 1985; (c) Gutsche, C. D. Calixarenes, Royal Society of Chemistry: London, 1989; (d) Diedrich, F. N. Cyclophanes, Royal Society of Chemistry: London, 1991; (e) Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 2495–2496; (f) Cram, D. J.; Cram, J. M. Container Molecules and Their Guests, Royal Society of Chemistry: London, 1994. 11. Atwood, J. L. Inclusion Phenomena and Molecular Recognition, Plenum Press: New York, 1988. 12. (a) Whitesides, G. M.; Grzybowski, B. Science 2002, 295, 2418–2421; (b) Boncheva, M.; A.Bruzewicz, D. Pure Appl. Chem. 2003, 75, 621–630; (c) Whitesides, G. M.; Mathias, J. P.; Seto, C. T. Science 1991, 254, 1312–1319; (d) Lindoy, L. F.; Atkinson, I. M. Self-assembly in Supramolecular Systems, Royal Society of Chemistry: Cambridge, 2000. 13. (a) Corbett, P. T.; Leclaire, J.; Vial, L.; West, K. R.; Wietor, J. L.; Sanders, J. K. M.; Otto, S. Chem. Rev. 2006, 106, 3652–3711; (b) Yeung, H. Y. A.; Pantos, G. D.; Sanders, J. K. M. PNAS 2009, 106, 10466–10470; (c) Cougnon, F. B. L.; Sanders, J. K. M. Acc. Chem. Res. 2012, 45, 2211–2221; (d) Belowicha, M. E.; Stoddart, J. F. Chem. Soc. Rev. 2012, 41, 2003–2024. 14. (a) Jena, N. K.; Murugan, N. A. J. Phys. Chem. C. 2013, 117, 25059–25068; (b) Ko, Y. H.; Hwang, I.; Kim, H.; Kim, Y.; Kim, K. Chem. Asian J. 2015, 10, 154–159; (c) Waelès, P.; Yaw, B. R.; Coutrot, F. Chem. Eur. J. 2016, 22, 6837–6845; (d) Goujon, A.; Mariani, G.; Lang, T.; Moulin, E.; Rawiso, M.; Buhler, E.; Giuseppone, N. J. Am. Chem. Soc. 2017, 139, 4923–4928. 15. Liu, Y.; Flood, A. H.; Bonvallet, P. A.; Vignon, S. A.; Northrop, B. H.; Tseng, H. R.; Jeppesen, J. O.; Huang, T. J.; Brough, B.; Baller, M.; Magonov, S.; Solares, S. D.; Goddard, W. A.; Ho, C. M.; Stoddart, J. F. J. Am. Chem. Soc. 2005, 127, 9745–9759. 16. Kudernac, T.; Ruangsupapichat, N.; Parschau, M.; Macia, B.; Katsonis, N.; Harutyunyan1, S. R.; Ernst, K. H.; Feringa, B. L. Nature 2011, 422, 759–765. 17. Rekharsky, M. V.; Inoue, Y. Chem. Rev. 1998, 98, 1875–1918. 18. Shohat, D.; Grushka, E. Anal Chem. 1994, 66, 747–750. 19. Pedersen, C. J. J. Am. Chem. Soc. 1967, 89, 7017–7036. 20. (a) Dietrich, B.; Lehn, J. M.; Sauvage, J. P.; Blanzat, J. Tetrahedron 1973, 29, 1629–1645; (b) Dietrich, B.; Lehn, J. M.; Sauvage, J. P. Tetrahedron 1973, 29, 1647–1658. 21. Cram, D. J.; Kaneda, T.; Helgeson, R. C.; Lein, G. M. J. Am. Chem. Soc. 1979, 101, 6752–6754. 22. (a) Loeb, S. J. Chem. Soc. Rev. 2007, 36, 226–235; (b) Crowley, J. D.; Goldup, S. M.; Lee, A. L.; Leigh, D. A.; McBurney, R. T. Chem. Soc. Rev. 2009, 38, 1530–1541; (c) Chambron, J. C.; Sauvage, J. P. Sci. China Chem. 2011, 54, 2028–2031; (d) Caballero, A.; Zapata, F.; Beer, P. D. Coord. Chem. Rev. 2013, 257, 2434–2455; (e) Bruns, C. J.; Stoddart, J. F. Acc. Chem. Res. 2014, 47, 2186–2199. 23. (a) Griffiths, K. E.; Stoddart, J. F. Pure Appl. Chem. 2008, 80, 485–506; (b) Niu, Z.; Gibson, H. W. Chem. Rev. 2009, 109, 6024–6046; (c) Beves, J. E.; Blight, B. A.; Campbell, C. J.; Leigh, D. A.; McBurney, R. T. Angew. Chem. Int. Ed. 2011, 50, 9260-9327; (d) Evans, N. H.; Beer, P. D. Chem. Soc. Rev. 2014, 43, 4658–4683; (e) Gil‐Ramírez, G.; Leigh, D. A.; Stephens Alexander, J. Angew. Chem. Int. Ed. 2015, 54, 6110–6150. 24. (a) Pentecost, C. D.; Chichak, K. S.; Peters, A. J.; Cave, G. W. V.; Cantrill, S. J.; Stoddart, J. F. Angew. Chem. Int. Ed. 2007, 46, 218–222; (b) Prakasam, T.; Lusi, M.; Elhabiri, M.; C, P. I.; Olsen, J. C.; Asfari, Z.; Cianferani-Sanglier, S.; Debaene, F.; Charbonniere, L. J.; Trabolsi, A., Angew. Chem. Int. Ed. 2013, 52, 9956–9960; (c) Ponnuswamy, N.; Cougnon, F. B. L.; Pantos, G. D.; Sanders, J. K. M. J. Am. Chem. Soc. 2014, 136, 8243–8251; (d) Schouwey, C.; Holstein, J. J.; R.; Scopelliti, K.; Zhurov, O.; Nagornov, K. O.; Tsybin, Y. O.; Smart, O. S.; Brigocne, G.; Severin, K. Angew. Chem. Int. Ed. 2014, 53, 11261–11265. 25. Leigh, D. A.; Pritchard, R. G.; Stephens, A. J. Nat. Chem. 2014, 6, 978–982. 26. (a) Chichak, K. S.; Cantrill, S. J.; Pease, A. R.; Chiu, S.-H.; Cave, G. W. V.; Atwood, J. L.; Stoddart, J. F. Science 2004, 304, 1308–1312; (b) Huang, S. L.; Lin, Y. J.; Li, Z. H.; Jin, G. X. Angew. Chem. Int. Ed. 2014, 53, 11218–11222. 27. Ayme, J. F.; Beves, J. E.; Leigh, D. A.; McBurney, R. T.; Rissanen, K.; Schultz, D. Nat. Chem. 2012, 4, 15–20; (b) Buchecker, C. O. D.; Sauvage, J. P. Angew. Chem. Int. Ed. Engl. 1989, 28, 189–192; (c) Ayme, J. F.; Beves, J. E.; Campbell, C. J.; Leigh, D. A. Chem. Soc. Rev. 2013, 42, 1700–1712; (d) Lukin, O.; Vogtle, F. Angew. Chem. Int. Ed. 2005, 44, 1456–1477; (e) Guo, J.; Mayers, P. C.; Breault, G. A.; Hunter, C. A. Nat. Chem. 2010, 2, 218–222. 28. (a) Wasserman, E. J. Am. Chem. Soc. 1960, 82, 4433–4434; (b) Wasserman, E. Sci. Am. 1962, 207, 94–102. 29. Schill, G.; Lüttringhaus, A. Angew. Chem. Int. Ed. 1964, 3, 546–547. 30. (a) Busch, D. H. J. Incl. Phen. 1992, 12, 389–395; (b) Busch, D. H.; Stephenson, N. A. Coord. Chem. Rev. 1990, 100, 119–154. 31. Beves, J. E.; Blight, B. A.; Campbell, C. J.; Leigh, D. A.; McBurney, R. T. Angew. Chem. Int. Ed. 2011, 50, 9260–9327. 32. Dietrich-Buchecker, C. O.; Sauvage, J. P.; Kern, J. M. J. Am. Chem. Soc. 1984, 106, 3043–3045. 33. Tung, S.-T.; Lai, C.-C.; Liu, Y.-H.; Peng, S.-M.; Chiu, S.-H. Angew. Chem. Int. Ed. 2013, 125, 13511–13272. 34. Wu, Y.-W.; Chen, P.-N.; Chang, C.-F.; Lai, C.-C.; Chiu, S.-H. Org. Lett. 2015, 17, 2158 –2161. 35. Fan, C.-F. Department of Chemistry, College of Science National Taiwan University Master Thesis 2015. 36. Hsu, C.-J. Department of Chemistry, College of Science National Taiwan University Master Thesis 2017. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/77793 | - |
dc.description.abstract | 本實驗室在先前的研究中發展出以鈉離子為模板,使含有二乙二醇鏈的二胺分子兩兩正交排列,並與二醛分子反應生成[2]交環烷的辨識系統。本研究主要希望利用導入二乙二醇鏈的合適互補基到大環結構中,製作出可以有效組裝異[2]交環烷的辨識系統。利用此一系統,我們可以簡單而有效率地(31%)合成出同時具有三個[2]交環烷分枝的高階異交環烷。 | zh_TW |
dc.description.abstract | Previously, we reported that Na+ ions can template the orthogonal alignment of two di(ethylene glycol)-containing diamines, which can then react with two units of dialdehyde to generate homo-[2]catenanes. In this study, we applied this strategy to the synthesis of hetero-[2]catenanes. By introducing a proper complementary unit for di(ethylene glycol) chain to the structures of the macrocycles, we are able to selectively assemble the desire hetero-[2]catenanes in solution. A stable [2]catenane trimer was synthesized directly from a simple hexa-aldehyde in 31% yield. | en |
dc.description.provenance | Made available in DSpace on 2021-07-11T14:34:57Z (GMT). No. of bitstreams: 1 ntu-107-R05223166-1.pdf: 3501330 bytes, checksum: 5153d57ac2349bbeec92d5a7faa57735 (MD5) Previous issue date: 2018 | en |
dc.description.tableofcontents | 摘要............i
Abstract........ii 圖目錄...........iv 流程目錄.........vi 表目錄...........vii 第一章、導論......1 1.1 前言..........1 1.2 主客化學與冠醚分子.......3 1.3 內鎖型分子 : 交環烷簡介.......6 第二章、結果與討論..........9 2.1 研究動機............9 2.2 設計合適互補基之大環誘導異[2]交環烷之合成........15 2.3 數個[2]交環烷分枝的高階異交環烷合成.........23 2.4 結論..........27 第三章、實驗部分...28 第四章、參考資料...40 第五章、附錄.......45 | |
dc.language.iso | zh-TW | |
dc.title | 具有多個[2]交環烷分枝之內鎖分子的合成研究 | zh_TW |
dc.title | The Synthesis of Interlocked Molecules with a Few [2]Catenane Branches | en |
dc.type | Thesis | |
dc.date.schoolyear | 106-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 徐秀福(Hsiu-Fu Hsu),李文山(Wen-Shan Li),陳平(Richard P. Cheng),賴建成(Chien-Chen Lai) | |
dc.subject.keyword | 超分子,交環烷, | zh_TW |
dc.subject.keyword | supramolecule,catenane, | en |
dc.relation.page | 67 | |
dc.identifier.doi | 10.6342/NTU201801505 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2018-07-13 | |
dc.contributor.author-college | 理學院 | zh_TW |
dc.contributor.author-dept | 化學研究所 | zh_TW |
dc.date.embargo-lift | 2028-07-13 | - |
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