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/123456789/76753
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.authorShin-Han Tsengen
dc.contributor.author曾信翰zh_TW
dc.date.accessioned2021-07-10T21:36:16Z-
dc.date.available2021-07-10T21:36:16Z-
dc.date.copyright2016-10-14
dc.date.issued2016
dc.date.submitted2016-07-21
dc.identifier.citation[1] Steed, J. W.; Atwood J. L.; Supramolecular Chemistry, 2nd ed, Wiley, 2009.
[2] (a) Whiteside, G. M.; Mathias, J. P.; Seto, C. T. Science 1991, 254, 1312; (b) Lindoy, L. F.; Atkinson, I. M.; Self-assembly in supramolecular sysytems, Springer Us/Rsc, 2000.
[3] (a) Lavigne, J. J.; Anslyn, E. V.; Angew. Chem. Int. Ed. 2001, 40, 3118; (b) Evans, N. H.; Beer, P. D.; Angew. Chem. Int. Ed. 2014, 53, 11716.
[4] (a) Valeur, B.; Leray, I.; Coord. Chem. Rev. 2000, 205, 3; (b) Rogers, C. W.; Worf, M. O.; Coord. Chem. Rev. 2002, 233-234, 341.
[5] (a) Rowan, S. J.; Cantrill, S. J.; Cousins, G. R. L.; Sanders, J. K. M.; Stoddart, J. F.; Angew. Chem. Int. Ed. 2002, 41, 898; (b) Cougnon, F. B. L.; Sanders, J. K. M.; Acc. Chem. Res. 2012, 45, 2211; (c) Belowicha,M. E.; Stoddart, J. F.; Chem. Soc. Rev. 2012, 41, 2003.
[6] (a) Ghadiri, M. R.; Granja, J. R.; Miligan, R. A.; McRee, D. E.; Khazanovich, N.; Nature 1993, 366, 324; (b) Whiteside, 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; (c) Zimmerman, S. C.; Zeng, F.; Reichert, D. E. C.;Kolotuchin, S. V.; Science 1996, 271, 1095; (d) Desiraju, G. R.; Chem. Commun. 2005, 2995.
[7] (a) Dougherty, D. A.; Science 1996, 271, 163. (b) Ma, J. C.; Dougherty, D. A.; Chem. Rev. 1997, 97, 1303. (c) Gokel, G. W.; De wall, S. L.; Meadows, E. S.; Eur. J. Org. Chem. 2000, 2967.
[8] (a) Dykstra, C. E.; Chem. Rev. 1993, 93, 2339; (b) Naray-Szabo, G.; Ferenczy, G.G.; Chem. Rev. 1995, 95, 829.
[9] (a) Chambron, J. C.; Chardon-Noblat, S.; Dietrich-Buchecker, C. O.; Heitz, V.; Sauvage, J. P.; Macrocycle Synthesis 1996, 207. (b) Fujita, M.; Umemoto, K.; Yoshizawa, M.: Fujita, N.; Kusukawa, T.; Biradha, K.; Chem. Commun. 2001, 509. (c) Kim, K.; Chem. Soc. Rev. 2002, 31, 96.
[10] (a) Southall, N. T.; Dill, K. A.; Haymet, A. D. J.; J. Phys. Chem. B 2002, 106, 521. (b) Chandler, D.; Nature 2005, 437, 640.
[11] Hunter, C. A.; Lawson, K. R.; Perkins, J.; Urch, C. J.; J. Chem. Soc., Perkin Trans. 2001, 651.
[12] (a) Andreetti, G. D.; Ungaro, R.; Pochini, A.; J. Chem. Soc., Chem. Commun. 1979, 1005. (b) Neusser, H. J.; Krause, H.; Chem. Rev. 1994, 94, 1829. (c) Desfrancois, C.; Carles, S.; Schermann, J. P.; Chem. Rev. 2000, 100, 3943.
[13] Pedersen, C. J.; J. Am. Chem. Soc. 1967, 89, 7017.
[14] Dietrich, B.; Lehn, J. M.; Sauvage, J. P.; Blanzat, J.; Tetrahedron 1973, 29, 1629.
[15] Cram, D. J.; Kaneda, T.; Helgeson, R. C.; Lein, G. M.; J. Am. Chem. Soc. 1979, 101, 6752.
[16] Lehn, J. M.; Cram, D. J.; Pedersen, C. J.; Nobel Lecture, 1987.
[17] (a) Ashton, P. R.; Baxter, I.; Cantrill, S. J.; Fyfe, M. C. T.; Glink, P. T.; Stoddart, J. F.; White, A. J. P.; Williams, D. J.; Angew. Chem. Int. Ed. 1998, 37, 9.
[18] Rotzlera, J.; Mayor, M.; Chem. Soc. Rev., 2013, 42, 44.
[19] Ashton, P. R.; Baxter, I.; Cantrill, S. J.; Fyfe, M. C. T.; Glink, P. T.; Stoddart, J. F. ; White, A. J. P.; Williams, D. J.; Angew. Chem. Int. Ed. 1998, 37, 9.
[20] Fujimoto, T.; Sakata, Y.; Kaneda. T.; Chem. Commun., 2000, 2143.
[21] Ashton, P. R.; Parsons, I. W.; Raymo,F. M.; Stoddart, J. F.; White, A. J. P.; Williams, D. J. ; Wolf, R.; Angew. Chem. Int. Ed. 1998, 37, 13.
[22] Strutt, N. L.; Zhang, H.; Giesener, M. A.; Leia, J.; Stoddart, J. F.; Chem. Commun. 2012, 48, 1647.
[23] (a) Zhang, Z.; Luo, Y.; Chen, J.; Dong, S.; Yu, Y.; Ma, Z.; Huang, F.; Angew. Chem. Int. Ed. 2011, 50, 1397; (b) Zhang, Z.; Yu, G.; Han, C.; Liu, J.; Ding, X.; Yu, Y.; Huang, F.; Org. Lett. 2011, 13, 18.
[24] Bruns, C. J.; Stoddart, J. F.; Acc. Chem. Res. 2014, 47, 2186.
[25] Jiménez, M. C.; Buchecker, C. D.; Sauvage, J. P.; Angew. Chem. Int. Ed. 2000, 39, 18.
[26] Fang, L.; Olson, M. A.; Benítez, D.; Tkatchouk, E.; Goddard III, W. A.; Stoddart, J. F.; Chem. Soc. Rev. 2010, 39, 17.
[27] Tsuda, S.; Aso, Y.; Kaneda, T.; Chem. Commun. 2006, 3072.
[28] Hoshino, T.; Miyauchi, M.; Kawaguchi, Y.; Yamaguchi, H.; Harada, A.; J. Am. Chem. Soc. 2000, 122, 40.
[29] (a) Kraus, T.; Buděšínský, M.; Cvačka, J.; Sauvage, J. P.; Angew. Chem. Int. Ed. 2006, 45, 258; (b) Voignier, J.; Frey, J.; Kraus, T.; Buděšínský, M.; Cvačka, J.; Heitz, V.; Sauvage, J. P.; Chem. Eur. J. 2011, 17, 5404.
[30] Schwab, P. F. H.; Fleisher, F.; Michl, J.; J. Org. Chem. 2012, 67, 443.
[31] Sugino, M.; Hatanaka, K.; Araki, Y.; Hisaki, I.; Miyata, M.; Tohnai, N.; Chem. Eur. J. 2014, 20, 3069.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/76753-
dc.description.abstract我們利用單元分子結構之剛硬性與金屬離子配位構形進行自組裝,專一性地合成出具功能性[c3]雛菊鏈( [c3]daisy chain ),並可藉由酸/鹼調控模擬生物肌肉”收縮 (contracted) ”和”舒張 (stretched)”的行為,有別於傳統分子肌肉線性運動,此為新穎二維分子肌肉之有機分子。zh_TW
dc.description.abstractDaisy chain is a daisy garland where the stems are interlocked to form a chain and chaplet. A molecular daisy chain is an array of identical molecules that must be designed in a way that two complementary sites recognize each other by intermolecular rather than intramolecular. In other words, the monomer must be prevent from ‘biting its own tail’ and lead to form a cyclic or acyclic daisy chains.
Herein, we report an artificial molecular muscle based on using structure rigidity, coordination geometries and bond rotational barriers to selectively form a [c3]daisy chains that operate as molecular switches through the acid/base condition to mimic the behavior of bio-muscle. Differing from the traditional linear behavior, it’s a novel two-dimensional molecular muscle.
en
dc.description.provenanceMade available in DSpace on 2021-07-10T21:36:16Z (GMT). No. of bitstreams: 1
ntu-105-R03223137-1.pdf: 10684326 bytes, checksum: 42248d4825d8bd0dc6e01871dbc58ae2 (MD5)
Previous issue date: 2016
en
dc.description.tableofcontents目錄
摘要 i
英文摘要 ii
目錄 iii
圖目錄 iv
流程目錄 vi
第一章、 導論 1
1.1 前言 1
1.2雛菊鏈 2
第二章、 結果與討論 4
2.1 研究動機 4
2.2 [c3]雛菊鏈之單體分子設計 10
2.3合成雛菊鏈之單體分子流程 11
2.4單體分子自組裝之研究 13
2.5 [c3]雛菊鏈與[c4]雛菊鏈分子之合成 18
2.6酸鹼控制[c3]雛菊鍊分子肌肉的行為研究 19
2.7結論 20
第三章、 實驗部分 21
第四章、 參考文獻 28
第五章、 附錄 31
dc.language.isozh-TW
dc.subject分子肌肉zh_TW
dc.subject配位化學zh_TW
dc.subject超分子化學zh_TW
dc.subject扭轉斥力zh_TW
dc.subject模板導引法zh_TW
dc.subject雛菊鏈zh_TW
dc.subjectcoordination chemistryen
dc.subjectdaisy chainen
dc.subjectmolecular muscleen
dc.subjecttemplate-directed synthesisen
dc.subjectsupramolecular chemistryen
dc.subjecttorsional strainen
dc.title二維分子肌肉之合成與研究zh_TW
dc.titleThe Two-Dimensional Molecular Muscle
Based on a [c3]Daisy Chain
en
dc.typeThesis
dc.date.schoolyear104-2
dc.description.degree碩士
dc.contributor.oralexamcommittee陳平(Richard P. Cheng),徐秀福(Hsiu-Fu Hsu),李文山(Wen-Shan Li),賴建成(Chien-Chen Lai)
dc.subject.keyword超分子化學,配位化學,分子肌肉,雛菊鏈,模板導引法,扭轉斥力,zh_TW
dc.subject.keywordsupramolecular chemistry,coordination chemistry,molecular muscle,daisy chain,template-directed synthesis,torsional strain,en
dc.relation.page50
dc.identifier.doi10.6342/NTU201601160
dc.rights.note未授權
dc.date.accepted2016-07-21
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-105-R03223137-1.pdf
  未授權公開取用
10.43 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