题名

具C3對稱三聚茆之衍生物的合成、性質及其在超分子化學上的應用

并列篇名

Synthesis and Properites of C3-symmetric Truxene-Based Derivates and Their Application in Supramolecular Chemistry

DOI

10.6342/NTU.2011.03447

作者

徐佳慧

关键词

三聚茆 ; 超分子化學 ; 有機凝膠分子 ; 分子辨識受體 ; Truxene ; Supramolecular Chemistry ; Organo Gelator ; Molecular Recognition Receptor

期刊名称

國立臺灣大學化學系學位論文

卷期/出版年月

2011年

学位类别

碩士

导师

汪根欉

内容语文

繁體中文

中文摘要

在本論文中,利用實驗室已發展出以三聚茚為主體C3對稱的立體骨架,即藉由在三聚茚C5、C10、C15號位置上修飾上苯環取代基創造出三維的架構中間體,用其獨特三維結構應用於超分子化學中。 第一部分合成有機凝膠分子TDMDA。利用在中間體上修飾具氫鍵作用力官能基及長碳鏈,發現在疏水性溶劑環己烷中可形成網狀結構的膠體,而在親水性甲醇溶劑中則形成奈米球微結構。同時我們藉由改變外自組裝外在環境,可在基板上直接轉換微結構。第二部分為分子辨識受體;係利用速配化學在中間體帶上具有π共軛苯環(TPTB、TDMTB)和芘的芳香環(TPTHP、TDMTHP)。利用1,2,3-三唑分子與鹵素離子間C-H…X-氫鍵作用力作為鹵素接受器,其中以氯的親和力最好。另外,藉由予體—受體的分子作用力,設計出與碳六十有良好作用力的受體分子。最後利用1H NMR及UV-Vis光譜滴定實驗證實。

英文摘要

In our previous studies, we developed an unique 3D skeleton based on truxene moiety. With incorporating various functional structures onto C5, C10, and C15 position of the truxene core, the successful synthetical strategy giving intriguing molecules through orthogonally and distinguishably modify active sites provides us an efficient way to further inspect on the diversity of its 3D derivatives. As a result, via involving the 3D truxene core, the thesis extend the applications of these various derivatives in supramolecular chemistry. Herein, we synthesized newly 3D organic gelator TDMDA which constructed by amide groups with long hydrocarbon chains. The morphology of TDMDA was found in fibrillar and globular morphology when dissolved in cyclohexane and methanol respectively and are characterized by SEM and TEM for close view. Moreover, gelator TDMDA incorporating amphipathic groups whose self-assembly display in-situ reversible transformation of aggregate morphology between fibrillar and globular upon exposure to different solvent. On the other hand, we also develope halide anion receptors TPTB and TDMTB from click chemistry. Accroding to NMR titration experiment, we found both of them have the best affinity to chloride due to the proper size of inner cavity. At last, we functionalized pyrene moiety onto the 3D architecture to achieve TPTHP and TDMTHP as C60 receptors, expecting it has good affinity with C60 via donor-acceptor and π-π interaction.

主题分类 基礎與應用科學 > 化學
理學院 > 化學系
参考文献
  1. 1 Lehn, J. M. Science, 1983, 219 ,1177.
    連結:
  2. 2 Lehn, J. M. Angew.Chem., Int. Ed. 1988, 27, 89.
    連結:
  3. 3 Dalgarno, S. J. Annu. Rep. Prog. Chem., Sect. B,
    連結:
  4. 4 D. K. Smith, Chem. Eur. J. 2005, 11, 5496.
    連結:
  5. 5 (a) Sangeetha, N. M.; Maitra, U. Chem. Soc. Rev. 2005,
    連結:
  6. Thordarson, P.; Braet, F. Chem. Asian J. 2011, 6, 30.
    連結:
  7. 6 Steed, J. W.; Atwood, J. L. Supramolecular Chemistry;
    連結:
  8. Wiley & Sons: Chichester, 2000.
    連結:
  9. Chem. Soc. 1994, 116, 6664.
    連結:
  10. Yu, Y.; Huang, F. Adv. Mater. 2012, 24, 362.
    連結:
  11. 9 Steed, J. W. Chem. Commun., 2011, 47, 1379.
    連結:
  12. Shinkai, S. Chem. Asian J. 2011, 6, 266.
    連結:
  13. Chem. Lett. 2010, 1, 3413.
    連結:
  14. Shimizu ,T. Chem. Mater.2012, 24, 209−214.
    連結:
  15. 13 Lei,T.; Cheng, C. Y.; Guo, Z. H.; Zheng, C.; Zhou,Y.;
    連結:
  16. Liang, D.; Pei , J. J. Mater.Chem. 2012, 22, 4306.
    連結:
  17. 14 (a) Ajayaghosh, A.; George, S. J. J. Am. Chem. Soc.
    連結:
  18. Eur. J. 2005, 11, 3217. (c)
    連結:
  19. 2008, 32, 2011.
    連結:
  20. Eur. J. 2012, 18, 5546.
    連結:
  21. 17 (a) Sandstrom, D.; Nygren, M.; Zimmermann, H.;
    連結:
  22. Chem. Eur. J. 1998, 4, 2129.
    連結:
  23. H.; Pei, J. J. Am. Chem. Soc. 2003, 125, 12430.
    連結:
  24. 19 Ma, H.; Jen, A. K. Y. Adv .Mater. 2001, 13, 1201.
    連結:
  25. J.; Pei, J. Chem. Eur. J. 2008, 14, 7760.
    連結:
  26. J.; Pei, J. J. Am. Chem. Soc. 2009, 131, 2076.
    連結:
  27. 22 Tseng, K.-P.; Kao, M.-T.; Tsai, Tim W. T.; Hsu, C.-H.;
    連結:
  28. Chem. Commum., 2012, 3515.
    連結:
  29. 23 高敏慈,國立台灣大學碩士論文,以三聚茚為主體之三維衍生物合成及其在超
    連結:
  30. 25 (a) Cametti, M.; Rissanen, K. Chem. Commun. 2009, 2809.
    連結:
  31. Org. Chem. 2004, 69, 6449.
    連結:
  32. Angew. Chem. Int.Ed. 2008, 47, 5038.
    連結:
  33. S. L. Angew. Chem. Int. Ed.2008, 47, 3740. (b) Meudtner,
    連結:
  34. R. M.; Hecht, S. Angew. Chem. Int. Ed. 2008, 47, 4926.
    連結:
  35. (c) Li, Y.; Huffman, J. C.; Flood, A. H. Chem. Commun.,
    連結:
  36. 2007, 2692.
    連結:
  37. Che, C.-M.; Li, Y.-L. Chem. Eur. J. 2012, 18, 4782.
    連結:
  38. 30 (a) Li , Y.; Flood, A. H. Angew. Chem. Int. Ed. 2008,
    連結:
  39. 47, 2649 (b) Li , Y.; Flood, A. H. J. Am. Chem. Soc.
    連結:
  40. 2008, 130, 12111.
    連結:
  41. Chem. Commun., 2012, 48, 2958.
    連結:
  42. 32 Steiner T. Acta Cryst. 1998, B54, 456.
    連結:
  43. H.; Nakamura, E.; Helene, C. Angew.Chem., Int. Ed. 1994,
    連結:
  44. Miyata, N. J. Org. Chem. 1996, 61, 7236.
    連結:
  45. 35 Kamat, J. P.; Devasagayam, T. P.; Priyadarsini, K. I.;
    連結:
  46. 145. (b) Sera, N.;Tokiwa, H.; Miyata, N. Carcinogenesis
    連結:
  47. 1996, 17, 2163.
    連結:
  48. 36 Okuda, K.; Mashino, T.;Hirobe, M. Bioorg. Med. Chem.
    連結:
  49. J.;Chiang, L. Y.Chem. Lett. 1998, 465.
    連結:
  50. 37 Royal Society of Chemistry: Cambridge, UK, 2007; Chapter
    連結:
  51. 38 Diederich, F.; Gomez-Lopez, M. Chem. Soc. Rev. 1999, 28,
    連結:
  52. Angew. Chem. 2004, 116,1754.; Angew. Chem. Int. Ed.
    連結:
  53. 2004, 43, 1722.
    連結:
  54. Chem. Soc. 2003,125,13934.
    連結:
  55. 41 Shirakawa, M.; Fujita, N.; Shinkai, S. J. Am. Chem. Soc.
    連結:
  56. 2003, 125, 9902.
    連結:
  57. Saigo, K.; Sakamoto, S.; Yamaguchi, K. J. Am. Chem. Soc.
    連結:
  58. Am. Chem. Soc. 2004, 126, 6570. (c) Shoji, Y.; Tashiro,
    連結:
  59. K.; Aida, T. J. Am. Chem. Soc. 2006, 128, 10690. (d)
    連結:
  60. Am. Chem. Soc. 2007, 129, 11912.
    連結:
  61. Anderson, H. L. Org. Lett., 2010, 15, 3544.
    連結:
  62. Chem. Soc. 2010, 132, 16356.
    連結:
  63. 45 Perez, E. M.; Sierra, M.; Sanchez, L.; Torres, M. R.;
    連結:
  64. Chem. 2007, 119, 1879.
    連結:
  65. Aida , T. J. Am. Chem. Soc. 2008, 130, 888.
    連結:
  66. Angew. Chem. Int. Ed. 2007, 46, 1847.
    連結:
  67. Angew. Chem. Int. Ed. 2008, 47, 1094.
    連結:
  68. M.; Martin, N. J. Am. Chem. Soc. 2011, 133, 3184
    連結:
  69. 50 Winnik, F. M. Chem. Rev. 1993, 93. 581.
    連結:
  70. Mullen, K. Chem. Rev. 2011, 111. 7260.
    連結:
  71. 52 Justin Thomas, K. R.; Thompson, A. L.; Sivakumar, A. V.;
    連結:
  72. Bardeen, C. J.; Thayumanavan, S. J. Am. Chem. Soc. 2005,
    連結:
  73. 2011,107,182.
  74. 34, 821. (b) Truong, W. T.; Su, Y.; Meijer, J. T.;
  75. 7 Murata, K.; Aoki, M.; Suzuki, T.; Harada, T.; Kawabata,
  76. H.; Komori, T.; Ohseto, F.; Ueda, K.; Shinkai, S. J. Am.
  77. 8 Yan, X.; Xu, D.; Chi, X.; Chen, J.; Dong, S.; Ding, X.;
  78. 10 Dawn, A.; Shiraki, T.; Haraguchi, S.; Tamaru, S. I.;
  79. 11 Babu, S. S.; Kartha, K. K.; Ajayaghosh, A. J. Phys.
  80. 12 Kameta, N.; Ishikawa, K.; Masuda, M.; Asakawa, Ma.;
  81. 2001, 123, 5148. (b) George, S. J.; Ajayaghosh, A. Chem.
  82. 15 Shi, N.; Yin, G.; Li, H.; Hana, M.; Xu, Z. New J. Chem.
  83. 16 Cao, H.; Duan, P.; Zhu, X.; Jiang, J.; Liu, M. Chem.
  84. Maliniakt, A. J. Phys. Chem. 1995, 99, 6661. (b) Perova,
  85. T. S.; Vij, J. K. Adv. Mater. 1995, 7, 919. (c) Lambert,
  86. C.; Noll, G.; Schamlzlin, E.; Meerholz, K.; Brauchle, C.
  87. 18 Cao, X.-Y.; Zhang, W.-B.; Wang, J.-L.; Zhou, X.-H.; Lu,
  88. 20 Wang, J.Y.; Yan, J.; Li, Z.; Han, J. M.; Ma,Y.; Bian,
  89. 21 (a) Luo, J.; Lei, T.; Wang, L.; Ma, Y.; Cao, Y.; Wang,
  90. Chen, J. C. C..; Shyue, J.-J.; Sum, S.-S.; Wong, K.-T.
  91. 分子應用探討,中華民國 98年7月
  92. 24 Kuo, M.-C.; Chen, H.-F.; Shyue, J.-J.; Bassani, D. M.;
  93. Wong, K.-T. Chem.Commum., 2012,48. 8051.
  94. 26 Nie, L.; Li, Z.; Han, J.; Zhang, X.; Yang, R.; Liu, W.-
  95. X.; Wu, F.-Y.; Xie, J.-W.;Zhao,Y.-F.; Jiang, Y.-B. J.
  96. 27 (a) Lee, C.-H.; Na, H.-K.; Yoon, D.-W.; Won, D.-H.; Cho,
  97. W.-S.; Lynch, V.M.;Shevchuk, S.V.; Sessler, J. L. J. Am.
  98. Chem. Soc. 2003, 125, 7301. (b) Yoon, D.-W.;Gross, D.
  99. E.; Lynch, V. M.; Sessler, J. L.; Hay, B. P.; Lee, C.-H.
  100. 28 (a) Juwarker, H.; Lenhardt, J. M.; Pham, D. M.; Craig,
  101. 29 Li, Y. -J.; Xu, L.; Yang ,W.-L.; Liu, H.-B.; Lai, S.-W.;
  102. 31 Yu, G.; Zhang, Z.; Han, C.; Xue, M.; Zhou, Q.; Huang, F.
  103. 33 Kroto, H. W.; Heath, J. R.;O’Brien, S. C.;Curl, R. F.;
  104. Smally, R. E. Nature (London) 1985, 318, 162.
  105. 34 (a) Boutorine, A. S.; Tokuyama, H.; Takasugi, M.; Isobe,
  106. 33, 2462. (b) Yamakoshi, Y. N.; Endo, T.; Sueyoshi, S.;
  107. Mohan, H.;Mittal, J. P. Chem. Biol. Interact. 1998, 114,
  108. Lett. 1996, 6, 539. (b) Chi,Y.;Bhonsle, J.
  109. B.;Canteenwala, T.;Huang, J.-P.; Shiea, J.;Chen, B.-
  110. 3, 4.
  111. 263.
  112. 39 Kawase, T.; Tanaka, K.; Shiono, N.; Seirai, Y.; Oda, M.
  113. 40 Yamaguchi, T.; Ishii, N.; Tashiro, K.; Aida, T. J. Am.
  114. 42 (a) Tashiro, K.; Aida, T.; Zheng, J. Y.; Kinbara, K.;
  115. 1999, 121, 9477 .(b) Shoji, Y.; Tashiro, K.; Aida, T. J.
  116. Yanagisawa,M.; Tashiro, K.; Yamasaki, M.; Aida, T. J.
  117. 43 Gil-Ramirez, G.; Karlen, S. D.; Shundo, A.; Porfyrakis,
  118. K.; Ito, Yasuhiro.; Briggs, G. A. D.; Morton, J. J. L.;
  119. 44 Song, J.; Aratani, N.; Shinokubo, H.; Osuka, A. J. Am.
  120. Viruela, R. Viruela, P. M.; Orti, E.; Martin, N. Angew.
  121. 46 Li, W.-S.; Yamamoto, Y.; Fukushima, T.; Saeki, A.; Seki,
  122. S.; Tagawa, S.; Masunaga, H.; Sasaki, S.; Takata, M.;
  123. 47 Perez, E. M.; Sierra, M.; Sanchez, L.; Rosario Torres,
  124. M.; l Viruela, R.; Viruela, P.M.; Orti, E.; Martin, N.
  125. 48 Fernandez, G.; Perez, E. M.; Sanchez, L.; Martin, N.
  126. 49 Canevet, D.; Gallego, M.; Isla, H.; Juan, A.; Perez, E.
  127. 51 (a) Cicchi, S.; Fabbrizzi, P.; Ghini, G.; Brandi, A.;
  128. Foggi, P.; Marcelli, A.; Righini, R.; Botta C. Chem.
  129. Eur. J. 2009, 15, 754. (b) Figueira-Duarte, T. M.;
  130. 127, 373.
  131. 53 Fujii, S.; Morita, T.; Kimura, S. Langmuir 2008, 24,
  132. 5608.