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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 | Ting-Jia Gu | en |
dc.contributor.author | 顧庭嘉 | zh_TW |
dc.date.accessioned | 2021-07-11T14:42:34Z | - |
dc.date.available | 2021-11-02 | |
dc.date.copyright | 2016-11-02 | |
dc.date.issued | 2016 | |
dc.date.submitted | 2016-08-17 | |
dc.identifier.citation | [1] (a) J. M. Lehn, Science 1993, 260, 1762–1763; (b) J. M. Lehn, Supramolecular chemistry : concepts and perspectives : a personal account built upon the George Fisher Baker non-resident lectureship in chemistry at Cornell University and the Lezione Lincee, Accademia nazionaleei [i.e. nazionale dei] Lincei, Roma, VCH, Weinheim ; New York, 1995.
[2] K. Muller-Dethlefs, P. Hobza, Chem. Rev. 2000, 100, 143–167. [3] (a) M. R. Ghadiri, J. R. Granja, R. A. Milligan, D. E. McRee, N. Khazanovich, Nature 1993, 366, 324–327; (b) R. P. Sijbesma, F. H. Beijer, L. Brunsveld, B. J. Folmer, J. H. Hirschberg, R. F. Lange, J. K. Lowe, E. W. Meijer, Science 1997, 278, 1601–1604; (c) S. C. Zimmerman, F. Zeng, D. E. Reichert, S. V. Kolotuchin, Science 1996, 271, 1095–1098; (d) J. Rebek, Acc. Chem. Res. 1999, 32, 278–286; (e) G. M. Whitesides, E. E. Simanek, J. P. Mathias, C. T. Seto, D. N. Chin, M. Mammen, D. M. Gordon, Acc. Chem. Res. 1995, 28, 37–44. [4] (a) D. G. Hamilton, J. E. Davies, L. Prodi, J. K. M. Sanders, Chem. Eur. J. 1998, 4, 608–620; (b) C. A. Hunter, J. K. M. Sanders, J. Am. Chem. Soc. 1990, 112, 5525–5534; (c) D. Philp, A. M. Z. Slawin, N. Spencer, J. F. Stoddart, D. J. Williams, J. Chem. Soc. Chem. Commun. 1991, 1584–1586. [5] (a) M. Fujita, K. Umemoto, M. Yoshizawa, N. Fujita, T. Kusukawa, K. Biradha, Chem. Commun. 2001, 509–518; (b) K. Kim, Chem. Soc. Rev. 2002, 31, 96–107. [6] (a) H. J. Neusser, H. Krause, Chem. Rev. 1994, 94, 1829–1843; (b) C. Desfrancois, S. Carles, J. P. Schermann, Chem. Rev. 2000, 100, 3943–3962. [7] (a) G. Narayszabo, G. G. Ferenczy, Chem. Rev. 1995, 95, 829–847; (b) C. E. Dykstra, Chem. Rev. 1993, 93, 2339–2353. [8] (a) L. R. Pratt, D. Chandler, J. Chem. Phys. 1977, 67, 3683–3704; (b) D. Chandler, Nature 2005, 437, 640–647. [9] (a) C. J. Pedersen, J. Am. Chem. Soc. 1967, 89, 2495–2496; (b) F. Vögtle, E. Weber, Host guest complex chemistry/macrocycles : synthesis, structures, applications, Springer, Berlin ; New York, 1985; (c) G. W. Gokel, Crown ethers and cryptands, Royal Society of Chemistry, Cambridge England, 1991; (d) D. J. Cram, J. M. Cram, Royal Society of Chemistry (Great Britain), Container molecules and their guests, Royal Society of Chemistry, Cambridge, 1994. [10] J. L. Atwood, Inclusion phenomena and molecular recognition, Plenum Press, New York, 1990. [11] (a) D. B. Amabilino, J. F. Stoddart, Chem. Rev. 1995, 95, 2725–2828; (b) T. J. Hubin, D. H. Busch, Coordin. Chem. Rev. 2000, 200, 5–52. [12] (a) G. M. Whitesides, J. P. Mathias, C. T. Seto, Science 1991, 254, 1312–1319; (b) L. F. Lindoy, I. M. Atkinson, Royal Society of Chemistry (Great Britain), Self-assembly in supramolecular systems, Royal Society of Chemistry, Cambridge, 2000. [13] I. T. Harrison, S. Harrison, J. Am. Chem. Soc. 1967, 89, 5723–5724. [14] H. Ogino, J. Am. Chem. Soc. 1981, 103, 1303–1304. [15] (a) A. Coskun, D. C. Friedman, H. Li, K. Patel, H. A. Khatib, J. F. Stoddart, J. Am. Chem. Soc. 2009, 131, 2493–2495; (b) A. Brown, K. M. Mullen, J. Ryu, M. J. Chmielewski, S. M. Santos, V. Felix, A. L. Thompson, J. E. Warren, S. I. Pascu, P. D. Beer, J. Am. Chem. Soc. 2009, 131, 4937–4952; (c) F. Durola, J. Lux, J. P. Sauvage, Chem. Eur. J. 2009, 15, 4124–4134; (d) E. Busseron, C. Romuald, F. Coutrot, Chem. Eur. J. 2010, 16, 10062–10073; (e) G. J. E. Davidson, S. Sharma, S. J. Loeb, Angew. Chem. Int. Ed. 2010, 49, 4938–4942; (f) T. Matsumura, F. Ishiwari, Y. Koyama, T. Takata, Org. Lett. 2010, 12, 3828–3831. [16] (a) D. A. Leigh, P. J. Lusby, R. T. McBurney, A. Morelli, A. M. Z. Slawin, A. R. Thomson, D. B. Walker, J. Am. Chem. Soc. 2009, 131, 3762–3771; (b) S. J. Li, M. Liu, B. Zheng, K. L. Zhu, F. Wang, N. Li, X. L. Zhao, F. H. Huang, Org. Lett. 2009, 11, 3350–3353; (c) W. D. Zhou, H. Y. Zheng, Y. J. Li, H. B. Liu, Y. L. Li, Org. Lett. 2010, 12, 4078–4081; (d) A. Altieri, V. Aucagne, R. Carrillo, G. J. Clarkson, D. M. D'Souza, J. A. Dunnett, D. A. Leigh, K. M. Mullen, Chem. Sci. 2011, 2, 1922–1928; (e) Y. T. Li, K. M. Mullen, J. Sardinha, V. Felix, P. D. Beer, Dalton Trans. 2011, 40, 12180–12190; (f) M. E. Belowich, C. Valente, R. A. Smaldone, D. C. Friedman, J. Thiel, L. Cronin, J. F. Stoddart, J. Am. Chem. Soc. 2012, 134, 5243–5261. [17] (a) F. M. Raymo, K. N. Houk, J. F. Stoddart, J. Am. Chem. Soc. 1998, 120, 9318–9322; (b) P. E. Mason, W. S. Bryant, H. W. Gibson, Macromolecules 1999, 32, 1559–1569; (c) A. M. Elizarov, T. Chang, S. H. Chiu, J. F. Stoddart, Org. Lett. 2002, 4, 3565–3568; (d) S. A. Vignon, T. Jarrosson, T. Iijima, H. R. Tseng, J. K. M. Sanders, J. F. Stoddart, J. Am. Chem. Soc. 2004, 126, 9884–9885; (e) S. Y. Hsueh, C. C. Lai, Y. H. Liu, Y. Wang, S. M. Peng, S. H. Chiu, Org. Lett. 2007, 9, 4523–4526; (f) M. A. Bolla, J. Tiburcio, S. J. Loeb, Tetrahedron 2008, 64, 8423–8427. [18] (a) C. W. Chiu, C. C. Lai, S. H. Chiu, J. Am. Chem. Soc. 2007, 129, 3500–3501; (b) S. H. Ueng, S. Y. Hsueh, C. C. Lai, Y. H. Liu, S. M. Penga, S. H. Chiu, Chem. Commun. 2008, 817–819; (c) J. L. Ko, S. H. Ueng, C. W. Chiu, C. C. Lai, Y. H. Liu, S. M. Peng, S. H. Chin, Chem. Eur. J. 2010, 16, 6950–6960. [19] (a) I. Yoon, M. Narita, T. Shimizu, M. Asakawa, J. Am. Chem. Soc. 2004, 126, 16740–16741; (b) S. Y. Hsueh, J. L. Ko, C. C. Lai, Y. H. Liu, S. M. Peng, S. H. Chiu, Angew. Chem. Int. Ed. 2011, 50, 6643–6646. [20] P. Terech, R. G. Weiss, Chem. Rev. 1997, 97, 3133–3159. [21] J. Raeburn, A. Z. Cardoso, D. J. Adams, Chem. Soc. Rev. 2013, 42, 5143–5156. [22] Y. L. Zhao, I. Aprahamian, A. Trabolsi, N. Erina, J. F. Stoddart, J. Am. Chem. Soc. 2008, 130, 6348–6350. [23] S. Y. Hsueh, C. T. Kuo, T. W. Lu, C. C. Lai, Y. H. Liu, H. F. Hsu, S. M. Peng, C. H. Chen, S. H. Chiu, Angew. Chem. Int. Ed. 2010, 49, 9170–9173. [24] C. Wang, Q. Chen, F. Sun, D. Q. Zhang, G. X. Zhang, Y. Y. Huang, R. Zhao, D. B. Zhu, J. Am. Chem. Soc. 2010, 132, 3092–3096. [25] (a) T. H. Ho, C. C. Lai, Y. H. Liu, S. M. Peng, S. H. Chiu, Chem. Eur. J. 2014, 20, 4563–4567; (b) S. T. Tung, C. C. Lai, Y. H. Liu, S. M. Peng, S. H. Chiu, Angew. Chem. Int. Ed. 2013, 52, 13269–13272. [26] M. Yamanaka, N. Haraya, S. Yamamichi, Chem. Asian J. 2011, 6, 1022–1025. | |
dc.identifier.uri | http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/78111 | - |
dc.description.abstract | 本研究中,我們利用實驗室先前所發表的系統,以鈉離子為模版,對一個具有尿素單元的分子進行辨識合成車輪烷。此尿素分子在未接上保護基的情況下可溶於水中並形成水凝膠,但在經由夾鎖法鎖上大環分子,形成車輪烷的結構後便可抑制其凝膠化作用。希望能將此系統做延伸,設計上一個可受光刺激斷裂的大環,讓此車輪烷分子可在接受光照後產生水凝膠。 | zh_TW |
dc.description.abstract | We reported a single urea functionality in a hydrogelator that could be“clipped”by a macrocycle generated from a diamine and a dialdehyde through the templating effect of a Na + ion. The interlocked macrocycle on the hydrogelator would restrained the solution from hydrogelizing. In addition, the ability to hydrogelize could be recovered by utilizing irradiation. | en |
dc.description.provenance | Made available in DSpace on 2021-07-11T14:42:34Z (GMT). No. of bitstreams: 1 ntu-105-R03223202-1.pdf: 4125337 bytes, checksum: 2b2e4f7f8b9d26445f29ccc3ccc5b9b0 (MD5) Previous issue date: 2016 | en |
dc.description.tableofcontents | 第一章、導論 1
1.1 前言 1 1.2 內鎖型分子:車輪烷 2 1.3 車輪烷分子的合成策略 3 1.3.1 早期車輪烷分子的合成 3 1.3.2 模版導引法 4 第二章、結果與討論 7 2.1 研究動機 7 2.2 車輪烷分子的設計 12 2.3 車輪烷分子合成測試 15 2.4 結論 22 第三章、實驗部分 23 第四章、參考文獻 33 附錄 37 | |
dc.language.iso | zh-TW | |
dc.title | 以車輪烷為架構之光致水凝膠研究 | zh_TW |
dc.title | A Photo-Triggerable Rotaxane-Based Hydrogel | en |
dc.type | Thesis | |
dc.date.schoolyear | 104-2 | |
dc.description.degree | 碩士 | |
dc.contributor.oralexamcommittee | 李文山(Wen-Shan Li),賴建成(Chien-Chen Lai),徐秀福(Hsiu-Fu Hsu),陳平(Richard Cheng) | |
dc.subject.keyword | 車輪烷,水凝膠, | zh_TW |
dc.subject.keyword | rotaxane,hydrogel, | en |
dc.relation.page | 51 | |
dc.identifier.doi | 10.6342/NTU201602952 | |
dc.rights.note | 有償授權 | |
dc.date.accepted | 2016-08-18 | |
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 |
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