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. 工學院
  3. 高分子科學與工程學研究所
請用此 Handle URI 來引用此文件: http://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33859
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陸天堯(Tien-Yau Luh)
dc.contributor.authorHui-Chun Yangen
dc.contributor.author楊慧君zh_TW
dc.date.accessioned2021-06-13T05:47:36Z-
dc.date.available2009-07-13
dc.date.copyright2006-07-13
dc.date.issued2006
dc.date.submitted2006-07-10
dc.identifier.citation第五章 參考文獻
1. Watson, J. D.; Crick, F. H. C. Nature (London) 1953, 171, 737.
2. (a) Schuster, G. B., Ed, Long-range Charge Transfer in DNA I & II (Springer Berlin) 2004.
(b) Fink, H.-W.; Schonenberger, C. Nature 1999, 398, 407.
3. Kasumov, A. Y.; Kociak, M.; Gueron, S.; Reulet, B.; Volkov, V. T. ; Klinov, D. V.; Bouchait, H. Science 2001, 291, 280.
4. Zwolak, M.; Ventra, M. D. Apple. Phys. Lett. 2002, 81, 925.
5. (a) Watson, J. D.; Crick, F. H. C. Nature (London) 1953, 171, 964. (b) Joyce, G. F. Nature 1989, 338, 217.
6. Orgel, L. E. Nature 1992, 358, 203.
7. Von Kiedrowski, G. Angew. Chem. Int. Ed. Engl. 1986, 25, 932. (b) Brandsch, R.; Luther, A.; Von Kiedrowski, G. Nature 1998, 396, 245. (c) Bag, B. G.; Von Kiedrowski, G. Pure & Appl. Chem. 1996, 68, 214.
8. Peins, L. J.; Reinhoudt, D. N.; Timmerman, P. Angew. Chem. Int. Ed. 2001, 40, 2382.
9. Tjivikua, T.; Ballester, P.; Rebek, J., Jr. J. Am. Chem. Soc. 1990, 112, 1249. (b) Feng, Q.; Park, P. K.; Rebek, J., Jr. Science, 1992, 256, 1179. (c) Conn, M. M.; Winter, E. A.; Rebek, J., Jr. Acc. Chem. Res. 1994, 27, 198.
10.Würthner, F; Rebek, J. Angew. Chem. Int. Ed. Engl. 1995, 34, 446.
11. Terfort, A.; Von Kiedrowski, G. Angew. Chem. Int. Ed. Engl. 1992, 31, 654.
12. Wang, B.; Sutherland, I. O. Chem. Commum. 1997, 1495.
13. (a) Harada, A.; Li, J.; Kamachi, M. Nature 1994, 370, 126. (b) Nagahama, S.; Matsumoto, A. J. Am. Chem. Soc. 2001, 123, 12176. (c) Berl, V; Huc, I.; Khoury, R. G.; Lehn, J.-M. Chem. Eur. J. 2001, 2810. (d) Schultheiss, N.; Powell, D. R.; Bosch, E. Inorg. Chem. 2003, 42, 8886. (e) Reger, D. L.; Semeniuc, R. F.; Rassolov, V.; Smith, M. D. Inorg. Chem. 2004, 43, 537. (f) Mohr, F.; Jennings, M. C.; Puddephatt, R. J. Angew. Chem. Int. Ed. 2004, 43, 969. (g) Orita, A.; Nakano, T.; An, D. L.; Tanikawa, K.; Wakamatsu, K.; Otera, J. J. Am. Chem. Soc. 2004, 126, 10389.
14. (a) Screen, T. E. O.; Thorne, J. R. G.; Denning, R. G.; Bucknall, D. G.; Anderson, H. L. J. Am. Chem. Soc. 2002, 124, 9712. (b) Tang, H.; Sun, J.; Jiang, J.; Zhou, X.; Hu, T.; Xie, P.; Zhang, R. J. Am. Chem. Soc. 2002, 124, 10482.
15. Grubbs, R. H.; Novak, B. M.; McGrath, D. M.; Benedicto, A.; France, M.; Nguyen, S. T. polym. Prepr. (Am. Chem. Soc., Div. Polym. Chem.) 1992, 33, 1225.
16. (a) Nguyen, S. T.; Grubbs, R. H. J. Am. Chem. Soc. 1992, 114, 3974. (b) Brown-Wensley, K. A.; Buchwald, S. L.; Canizzo, L.; Clawson, L.; Ho, S.; Meinhardt, D.; Still, J. R.; Strauss, D.; Grubbs, R. H. Pure Appl. Chem. 1983, 55, 1733. (c) Canizzo, L. F.; Grubbs, R. H. Macronmlecules 1987, 20, 1488. (d) Grubbs, R. H. In Comprehensive Organometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E., Eds; Pergamon: Oxford. 1982, Vo18.
17. (a) Weskamp, T.; Schattenmann, W. C.; Spiegler, M.; Herrmann, W. A. Angew. Chem. Int. Ed. 1998, 110, 2631. (b) Weskamp, T.; Schattenmann, W. C.; Spiegler, M.; Herrmann, W. A. Angew. Chem. Int. Ed. 1998, 37, 2490. (c) Ackerman, L.; Fürstner, A. Weskamp, T.; Kohl, F. J.; Herrmann, W. A. Tetrahedron Lett. 1999, 40, 4787. (d) Scholl, M.; Trnka, T. M.; Morgan, J. P.; Grubbs, R. H. Tetrahydrogen Lett. 1990, 40, 2247. (e) Scholl, M.; Trnka, T. M.; Morgan, J. P.; Grubbs, R. H. Tetrahydrogen Lett. 1999, 40, 2247.
18. Schneider, M. F.; Blechert, S. Angew. Chem. Int. Ed . 1996, 35, 411.
19. Ivin, K. J.; Mol, J. C. Olefin Metathesis and Metathesis Polymerization; Academic Press, 1997.
20. Boyd, T. J.; Geerts, Y.; Lee, J.-K.; Fogg, D. E.; Lavoie, G. G.; Schrock, R. R.;
Rubner, M. F. Macromolecules 1997, 30, 3553.
21. Walba, D. M.; Keller, P. Shao, R.; Clark, N. A.; Hillmyer, M.; Grubbs, R. H. J. Am. Chem. Soc. 1996, 118, 2740.
22. (a) Sattigeri, J. A.; Shiau, C. -W.; Yeh, F. F.; Jin, B. -Y.; Hsu, C. C.; Luh, T. -Y. J. Am. Chem. Soc. 1999, l2l, 1607. (b) Shiau, C. -W.; Sattigeri, J. A.; Shen, C. K. -F.; Luh, T. -Y . Organometallics 1999, 572, 291. (d) Hsu, C. C.; Hung, T. -H.; Liu, S.; Yeh, F. -F.; Jin. B. -Y.; Sattigeri, J. A.; Shiau, C. -W.; Luh, T. -Y. Chem. Phys. Lett. 1999, 311, 355. (e) Churikov, V.; Hung, M. -F.; Hsu, C. C.; Shiau, C. -W.; Luh, T. -Y. Chem. Phys. Lett. 2000, 322, 19. (f) Luh, T. -Y.; Chen, R. -M.; Hung, T. -Y.; Basu, S.; Shiau, C. -W.; Lin, W. -Y.; Jin, B. -Y.; Hsu, C. C. Pure. Appl. Chem. 2001, 73, 243. (g) 蕭崇瑋, 國立台灣大學化學研究所碩士論文, 1999. (h) Lin, W.-Y.; Murugesh, M. G.; Sudhakar, S.; Yang, H.-C.; Tai, H.-C.; Chang, C.-S.; Liu, Y.-H.; Wang, Y.; Chen, I.-W. P.; Chen, C.-H.; Luh, T.-Y. Chem. Eur. J. 2006, 12, 324.
23. 林韋佑,國立台灣大學化學研究所博士論文,2006。
24. 林韋佑,國立台灣大學化學研究所碩士論文,2001。
25. Robert, K. B.; Arne, H. J. Organometal. Chem. 1966, 5, 470.
26. Grubbs, R. H. Handbook of Metathesis; Wiley- VCH: Weinheim, 2003.
27. 電腦模擬的部分是由本實驗室博士後研究員楊小青博士所完成。
28. Lin, S. H; Alden, R.; Islampour, Ma, R. H.; Villaeys, A. A. Density Matrix Method and Femtosecond Processes, World Scientific, 1991. Yang, H.-C.; Hua, C. -Y.; Kuo, Ming-Yu; Huang, Q.; Chen, C.-L. Chem. Phys. 2004, 5, 373.
29. Ho, N. F.; Mak, T. C. W.; Luh, T.-Y. J. Chem. Soc. Dalton Trans. 1990, 3591.
30. Yang, H.-C.; Lin, S.-M.; Liu, Y.-H.; Wang, Y.; Chen, M.-M.; Sheu, H.-S.; Tsou, D.-L.; Lin, C.-H.; Luh, T.-Y. J. Organometal. Chem. 2006, 0000.(in press)
31. Walba, D. M.; Keller, P.; Shao, R.; Clark, N. A.; Hillmyer, M.; Grubbs, R. H. J. Am. Chem. Soc. 1996, 118, 2740.
32. 蔡綸,國立台灣大學化學研究所碩士論文,2002。
33. Yang, H.-C.; Lin, S.-Y.; Yang, H.-C.; Lin, C.-L.; Tsai, L.; Huang, S.-L.; Chen, I.-W. P.; Chen, C.-H.; Jin, B.-Y.; Luh, T.-Y. Angew. Chem. Int. Ed. 2006, 45, 726.
34. Togin, A.; Hayashi, T. Ferrocene; VCH, 1995.
35. Dunitz, J. D.; Orgel, L. E.; Rich, A. Acta Crystallogr. 1956, 9, 373.
36. (a) Shin, D.-M.; Lee, I.-S.; Chung, Y.-K. Eur. J. Inorg. Chem. 2003, 2311. (b) Dirksen, A.; Hahn, U.; Schwanke, F.; Nieger, M.; Reek, J. N. H.; Vogtle, F.; Cola, L.D. Chem. Eur. J. 2004, 10, 2036.
37. Meier, H. Angew. Chem. Int. Ed. 2005, 44, 2482.
38. Smith, J. R. L.; Linford, J. M.; Mckeer, L. C.; Morris, P. M. J. Chem. Soc. Perkin Trans. 2, 1984, 1099.
39. Clemmer, C.R.; Beebe, T. P. Jr. Science 1991, 251, 640.
40. Drew, H. R.; Samson, S.; Dickerson, R. E. Proc. Nat. Acad. Sci. 1982, 79, 4040.
41. Wang, A. H. –J.; Quigley, G. J.; Kolpak, F. J.; Marel, G. Van der.; Boom, J. H. Van; Rich, A. Science 1981, 211, 171.
42. 電化學的分析是本實驗室由博士後研究員林正嵐博士所完成。
43. Schwink, L.; Knochel, P. Chem. Eur. J. 1998, 4, 950.
44. Corey, E. J.; Bakshi, R.; Shibata, S.; Chen, C.; Singh, V. J. Amer. Chem. Soc. 1987, 109, 7925.
45. (a) Schwink, L.; Knochel, P. Tetrahedron Lett. 1996, 37, 25. (b) Locke, A. J.; Richards, C. J. ibid. 1996, 37, 7861.
46. Wright, J.; Frambes, L. Reeves, P. J. Organometal. Chem. 1994, 476, 215.
47. Kim, T.-J.; Lee, H.-Y.; Ryu, E.-S.; Park, D.-K.; Cho, C. S.; Shim, S. C.; Jeong, J. H. J. Organometal. Chem. 2002, 649,258.
48. Takahashi, S. Angew. Chem. Int. Ed. 2003, 42, 4349.
49. Harada, N.; Nakanishi, K. Circular Dichroic Spectroscopy: Exciton Coupling in Organic Stereochemistry, University Science Books, Mill Valley, CA, 1983.
50. Ryttel, A. Angew. Makro. Chem. 1999, 267, 67.
51. Salakhov, M. S.; Musaevq, N. F.; Suleimanov, S. N.; Bairamov, A. A. J. Org. Chem. 1979, 15, 2106.
52. Carlstrom, A.-S.; Frejd, T. J. Org. Chem. 1990, 55, 4175.
53. Sato, H.; Watanabe, H.; Ohtsuka, Y.; Ikeno, T.; Fukuzawa, S.-I.; Yamada, T. Org. Lett, 2002, 4, 3313.
54. Locke, A.-J.; Richards, C. J. Organometallics. 1999, 18, 3750.
55. Karaman, R.; Almarsson, O.; Blasko, A.; Bruice, T. C. J. Org. Chem. 1992, 57, 2169.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/33859-
dc.description.abstract利用Grubbs-I催化的開環歧化反應,含二茂鐵之雙二環〔2.2.1〕庚烯骨架的衍生物可以合成一系列的雙股螺旋高分子。藉由單體的精心設計,雙股高分子具有一定的剛性,架橋於雙股之連接基團中的二茂鐵又使雙股高分子有一些柔軟性。另外,利用鹼基促進高分子的水解可得到相對高產率的二條單股高分子和連接基團,二羰酸二茂鐵。STM(Scanning Tunneling Microscopy)觀察雙股高分子得到螺旋狀(helical structure),超螺旋(supercoil)和梯狀(ladder)三種結構和理論計算的結果相符。雙股高分子和DNA的結構相似,它們有相似的寬度,每一段有相似的重覆單元的數量,雙股高分子的五環垂直於連接基團而且相鄰二個單體間也具有相似的距離,這些結果暗示著我們所合成的高分子是類似DNA 結構的雙股螺旋高分子。
另一方面,我們合成出一系列具手性的雙股高分子,由吸收光譜的藍位移證明高分子中存在發色團間的相互作用,由圓二色性光譜 (circular dichroism) 測量,各別單體和高分子的鏡向異構物的圓二色性性質,發現手性中心 (chiral center) 的取代基是主要影響手性單體和手性雙股高分子的圓二性光譜性質的主要因素,在一些例子當中,雙股高分子的圓二色性光譜強度大於手性單體,這些結果暗示著手性雙股高分子的螺旋性增加。
zh_TW
dc.description.abstractThe synthesis of a series of helical double strand polymers containing ferrocene moiety by ring opening metathesis polymerization (ROMP) of a bisnorbornene derivative is described. Ferrocene moiety was incorporated as part of the linker since it has certain rigidity but is somewhat flexible. Base-promoted hydrolysis of this polymer affords the corresponding single stranded polymer and the linker, ferrocene-1,1’-dicarboxylic acid, in excellent yield. Three forms (helical, supercoil and ladder) of the polymer have been observed by STM and simulated by molecular mechanical and dynamical calculations. The polymer thus obtained resembles structurally to DNA by having similar width, number of monomeric units per pitch, five-membered rings in the polymeric frame, perpendicular linkers to the backbones, and similar spacing between neighboring monomeric units. These results suggest that the polymers may adopt our proposed DNA-like double stranded structures.
On the other hand, A series of chiral double stranded polymers were designed and synthesized. Between chromophores interaction may occur as evidenced by the blue shift of the absortion maximum. A pair of enantiomeric double stranded monomers and polymers was subjected to CD measurements. Substitute of chiral center may appear to be the pivotal factor to dictate the CD properties of chiral double stranded monomers and polymers. The CD intensity of chiral double stranded polymers is enhancement than monomers. These results suggest that the helixty of chiral double stranded polymers may increased.
en
dc.description.provenanceMade available in DSpace on 2021-06-13T05:47:36Z (GMT). No. of bitstreams: 1
ntu-95-D92549007-1.pdf: 5981401 bytes, checksum: f279b8c66bcd2468d4f9402907eed80d (MD5)
Previous issue date: 2006
en
dc.description.tableofcontents謝誌…………………………………………………………………………………….I
中文摘要……………………………………………………………………………....II
英文摘要……………………………………………………………………………...III
章節目錄…………………………………………………………...............................IV
表目錄………………………………………………………………………………...VI
圖目錄………………………………………………………………………………..VII縮寫對照表…………………………………………………………………………....X
化合物縮寫對照表.......................................................................................................XI
發表在Angew. Chem. Int. Ed. 2006, 45, 726.的插畫……………………………….XII
第一章 緒論………………………………………………………………………....1
1-1前言……………………………………………………………………………..1
1-2形成雙股高分子的策略與方法………………………………………………10
1-3雙股高分子的初探…………………………………………………………....20
第二章 結果與討論………………………………………………………………..26
2-1二茂鐵連接基團之雙股螺旋高分子…………………………………………26
2-2二茂鐵酯類連接基團之雙股螺旋高分子的合成策略………………………26
2-2-1具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)雙酯類衍生物之雙股螺旋高分子Fc1P的合成與鑑定………………………………………..29
2-2-2具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)雙酯類衍生物之雙股螺旋高分子Fc1P的物理性質的探討…………………………………..47
2-3二茂鐵亞甲基酯類連接基團之雙股螺旋高分子……………………………49
2-3-1具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)亞甲基酯類衍生物之雙股螺旋高分子Fc2P的合成與鑑定…………………………………..50
2-3-2具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)亞甲基酯類衍生物之雙股螺旋高分子Fc2P的物理性質的探討……………………………..59
2-4具手性(Chiral)二茂鐵亞甲基酯類聯結基團之雙股螺旋高分子………..60
2-4-1具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)亞甲基酯類衍生物手性雙股螺旋高分子的合成........................................................................62
2-4-2具雙二環[2.2.1]庚烯骨架二茂鐵(Ferrocene)亞甲基酯類衍生物手性雙股螺旋高分子的鑑定……………………………………………....68
第三章 結論………………………………………………………………………..86
第四章 實驗部分…………………………………………………………………..88
4-1測試儀器………………………………………………………………………88
4-2實驗步驟………………………………………………………………………90
第五章 參考文獻…………………………………………………………………130
附錄A………………………………………………………………………………135
化合物之1H NMR 光譜
附錄B………………………………………………………………………………171
部分化合物之VT-1H NMR 光譜
dc.language.isozh-TW
dc.subject螺旋結構zh_TW
dc.subject掃描式穿隧電子顯微鏡zh_TW
dc.subject雙股高分子zh_TW
dc.subjectSTMen
dc.subjectDouble stranded polymeren
dc.subjectHelical structueren
dc.title如DNA般的雙股高分子zh_TW
dc.titleDNA-like Double Stranded Polymersen
dc.typeThesis
dc.date.schoolyear94-2
dc.description.degree博士
dc.contributor.oralexamcommittee陳文章(Wen-Chang Chen),陳俊顯(Chun-Hsien Chen),梁文傑(Man-Kit Leung),林江珍(Jiang-Jen Lin),周大新(Tahsin J. Chow)
dc.subject.keyword螺旋結構,雙股高分子,掃描式穿隧電子顯微鏡,zh_TW
dc.subject.keywordHelical structuer,Double stranded polymer,STM,en
dc.relation.page175
dc.rights.note有償授權
dc.date.accepted2006-07-11
dc.contributor.author-college工學院zh_TW
dc.contributor.author-dept高分子科學與工程學研究所zh_TW
顯示於系所單位:高分子科學與工程學研究所

文件中的檔案:
檔案 大小格式 
ntu-95-1.pdf
  未授權公開取用
5.84 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