簡易檢索 / 詳目顯示

研究生: 陳志銘
CHIH-MING CHEN
論文名稱: 含氮硫多牙基之ㄧ價銅和二價銅錯合物的合成、結構與藍銅蛋白活性中心之相關研究
Syntheses and Structures of Copper(I) and Copper(II)Complexes with N/S Multidentate Ligands:Relevance to the Active Site of Blue Copper Proteins
指導教授: 李位仁
Lee, Way-Zen
蘇展政
Su, Chan-Cheng
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2007
畢業學年度: 95
語文別: 中文
論文頁數: 97
中文關鍵詞: 藍銅蛋白
英文關鍵詞: blue copper protein
論文種類: 學術論文
相關次數: 點閱:164下載:0
分享至:
查詢本校圖書館目錄 查詢臺灣博碩士論文知識加值系統 勘誤回報
  • 藍銅蛋白具有電子傳遞的功能,其活性中心的二價銅離子配位兩個His和一個Cys形成一個三角平面,與軸位上配位的Met成為扭曲的四面體結構。本研究以兩個含氮硫三牙基BBMeMS、BBMeES為主要配子,分別合成了二價銅錯合物[Cu(BBMeMS)(CH3CN)2(H2O)](ClO4)2 (1)、[Cu(BBMeES)(CH3CN)(η1-ClO4)](ClO4) (2)作為起始物,再將二價銅錯合物1、2分別與一系列不同的硫化物反應以模擬藍銅蛋白的活性中心。若在室溫下反應,可分別得到無色的一價銅錯合物[Cu(η2-BBMeMS)- (CH3CN)](ClO4) (7)、[Cu(CH3CN)(μ-BBMeES)Cu(BBMeES)](ClO4)2 (8);然而,若在-78℃下反應,可產生深藍色的產物。當二價銅錯合物1與Sodium diethyldithiocarbamate反應,可以分離得到diethyldithiocarbamate配位的二價銅錯合物[Cu(BBMeMS)((C2H5)2NCS2)](ClO4)2 (3)以及一價銅錯合物7。我們也嚐試模擬還原態的藍銅蛋白活性中心,將一價銅錯合物8分別加入去質子化的硫化物thiobenzoate以及2-(trimethylsilyl)benzene- thiolate,並且藉由核磁共振光譜的鑑定,推測有錯合物[Cu(BBMeES)- (C6H5COS-)]與[Cu(BBMeES)((CH3)3SiC6H4S-)]的生成。
    此外,我們也合成了兩個雙牙基的配子: 1-methyl-2-(methylthio- methyl)-1H-benzimidazole (MMB)、Sodium (1-methylbenzimidazol-2-yl)- methanethiolate (L2)來嘗試模擬藍銅蛋白的活性中心,過程中得到了已發表的二價銅錯合物[(η2-MMB)2Cu(η1-ClO4)](ClO4) (6)以及一價銅錯合物[(η2-MMB)(η1-MMB)Cu](ClO4) (9)。
    本研究的結果發現,以電中性的含氮硫雙牙或三牙基所合成的二價銅化合物與去質子化的硫化物反應時,銅金屬中心容易被還原成ㄧ價銅離子。如何設計的可穩定二價銅中心的適當配位基將是合成藍銅蛋白擬態分子的成功關鍵。

    The active site of the well known electron transferase blue copper protein, has a distorded tetrahedral geometry, which the Cu ion is coordinated to two histidine and one cysteine in an approximately trignoal plane and to a methionine at the axial position. In this study, we have synthesized the Cu(II) complexes, [Cu(BBMeMS)(CH3CN)2(H2O)](ClO4)2 (1) and [Cu(BBMeES)(CH3CN)(η1-ClO4)](ClO4) (2) by the reaction of Cu(ClO4)2•6H2O with the N2S(thioether) ligands, BBMeMS and BBMeES, respectively, to be the precursor to prepare synthetic mimics for the active site of the blue copper protein. As Cu(II) complexe 1 and 2 reacted with a series of thiolate ligands, colorless Cu(I) complexes, [Cu(η2-BBMeMS)- (CH3CN)](ClO4) (7) and [Cu(CH3CN)(μ-BBMeES)Cu(BBMeES)](ClO4)2 (8) were obtained at room temperature; whereas, a deep blue solution was observed at - 78℃. When Cu(II) complex 1 reacted with sodium diethyldit- hiocarbamate, a diethyldithiocarbamate coordinated Cu(II) complex [Cu- (BBMeMS)((C2H5)2NCS2)](ClO4)2 (3) and a Cu(I) complex 7 were isolated. We have also attempted to model the active site of the reduced form of blue copper protein by reacting complex 8 with thiobenzoate and 2-(trimethylsilyl)benzenethiolate , respectively. From NMR analysis of the products, two Cu(I)-thiolate complex [Cu(BBMeES)(C6H5COS-)] and [Cu(BBMeES)((CH3)3SiC6H4S-)] were expected.
    In addition, we have prepared two bidentate ligand: 1-methyl-2-(methy- lthiomethyl)-1H-benzimidazole (MMB) and Sodium(1-methylbenzimidazol- 2-yl)methanethiolate (L2) for modeling the active site of blue copper protein. We have obtained a Cu(II) complex [(η2-MMB)2Cu(η1-ClO4)](ClO4) (6) and a Cu(I) complex [(η2-MMB)(η1-MMB)Cu](ClO4) (9).
    In summary, we found that the thiolate ligands have a very high tendence to reduce a Cu(II) ion which were coordinated to the neutral bidentate or tridentate N/S ligands. It is very crucial to design an appropriate ligand, which can stabilized a Cu(II) ion, to mimic the coordination environment of the active site of blue copper protein.

    中文摘要…………………………………………………………………Ι 英文摘要…………………………………………………………………Ⅲ 圖索引……………………………………………………………………Ⅴ 表索引……………………………………………………………………Ⅷ 附錄索引…………………………………………………………………Ⅸ 第一章 緒論 第一節 藍銅蛋白的簡介………………………………………………1 第二節 模擬藍銅蛋白的相關文獻……………………………………8 第三節 ㄧ價銅與二價銅錯合物基本結構的性質……………………15 第四節 研究動機與目標………………………………………………19 第二章 實驗部分 第一節 實驗儀器、藥品及條件………………………………………20 第二節 配位基的合成與鑑定…………………………………………27 第三節 二價銅錯合物的合成…………………………………………34 第四節 一價銅錯合物的合成…………………………………………38 第五節 以含氮硫三牙基銅錯合物模擬藍銅蛋白……………………41 第六節 以含氮硫二牙基模擬藍銅蛋白………………………………50 第三章 結果與討論 第一節 配子合成的討論………………………………………………53 第二節 錯合物的結果與探討…………………………………………56 第三節 錯合物的電子吸收光譜討論…………………………………70 第四節 二價銅錯合物與硫醇鹽反應之探討…………………………72 第五節 二價銅錯合物還原電位之探討………………………………79 第六節 二價銅錯合物與硫醇鹽反應之探討…………………………84 第七節 以含氮硫二牙基模擬藍銅蛋白活性中心的討論……………91 第四章 結論與展望……………………………………………………93 參考文獻…………………………………………………………………95

    1. Nar, H.; Messerschmidt, A.; Huber, R.; van de Kamp, M.;
    Canters, G. W. J. Mol. Biol.1991, 221, 765.
    2. Kitajima, N.; Fujisawa, K.; Tanaka, M. Adv. Inorg. Chem.
    1992, 39, 1.
    3. Ramshaw, J. A. M. Nature, 1978, 272, 319.
    4. Lippard, S. J. Principle Of Bioinorganic chemisrtry;
    University Science Books: Mill Vally, 1994, p 86 and
    p 237-242.
    5. Solomon, E. I.; Szilagyi, R. K.; George, S. D.;
    Basumallick, K. Chem. Rev. 2004, 104, 419.
    6. Solomon, E. I.; Sundaram, U. M.; Machonkin, T. E. Chem.
    Rev. 1996, 96, 2563.
    7. Holm, R. H.; Solomon, E. I.; Kennepohl, P. Chem. Rev.
    1996, 96, 2239.
    8. Messerschmidt, A. J. Mol. Biol. 1989, 206, 513.
    9. Chang, T. K. ; Rodrigues, C. G.; Kiserf, C. N.; Lew, A.
    Y. C.; Germanas, J. P.; Richards, J. H.; Iverson, S. A.
    PNAS , 1991, 88, 1325.
    10. Honek, J. F.; Lu, Y.; Garner, D. K.; Vaughan, M. D.;
    Hwang, H. J.; Savelieff, M. G.; Berry, S. M.J. Am.
    Chem. Soc., 1977, 128, 15608. 表格資料來自此篇Supporting
    information
    11. Gray, H. B.; Richards, J. H.; Machczynski, M.C. J.
    Inorg. Biochem. 2002, 88, 375.
    12. Gray, H. B.; Malmström, B. G.; Williams, R. J. P. J.
    Biol. Inorg. Chem. 2000, 5, 551.
    13. Gray, H. B.; Crane, B. R.; Di Bilio, A. J.; Winkler, J.
    R. J. Am. Chem. Soc. 2001, 123, 11623.
    14. Thompson, J. S.; Marks, T. J.; Ibers, J. A. Proc. Natl.
    Acad. Sci. USA, 1977, 74, 3114.
    15. Marks, T. J.; Ibers, J. A.; Thompson, J. S. J. Am.
    Chem. Soc. 1979, 101, 4180.
    16. Kitajima, N; Moro-oka, Y.; Fujisawa, K. J. Am. Chem.
    Soc. 1990, 112, 3210.
    17. Kitajima, N.; Fujisawa, K.; Tanaka, M.; Moro-oka, Y. J.
    Am. Chem. Soc, 1992; 114, 9232.
    18. Qiu, D.; Kilpatrick, L.; Kitajima, N.; Spiro, T. G. J.
    Am. Chem. Soc. 1994, 116, 2585.
    19. Tolman, W. B.; Holland, P. L. J. Am. Chem. Soc. 1999,
    121, 7270.
    20. Holland, P. L.; Tolman, W. B. J. Am. Chem. Soc. 2000,
    122, 6331.
    21. Fujisawa, K.; Matsunaga, Y.; lbi, N.; Miyashita, Y.;
    Okamoto, K. Inorg. Chem.2005, 44, 325.
    22. 蔡秀緣,國立台灣師範大學化學研究所碩士論文,2002.
    23. Clifford, A. M.; Lichty, J. G.. J. Am. Chem. Soc. 1932,
    54, 1163. 24. Casella, L.; Gullotti, M.; Suardi, E. J.
    Chem. Soc. Dalton Trans. 1990, 2843.
    25. Casella, L.; Gullotti, M.; Pintar, A.; Pinciroli, F.;
    Viganò, R. J. Chem. Soc. Dalton Trans. 1989, 1161.
    26. Milner, E. S.; jun.; Snyder, S.; Joullié, M. M. J.
    Chem. Soc. 1964, 4151.
    27. Kaim,W.; Albrecht, M.; Hübler, K.; Scheiring, T. Inorg.
    Chim. Acta 1999, 287, 204.
    28. Block, E.; Eswarakrishnan, V.; Gernon, M.; Ofori-Okai,
    G.; Saha, C.; Tang, K.; Zubieta, J. J. Am. Chem. Soc.
    1989, 111, 658.
    29. Wilson, J. M.; Bayer, R. J.; Hupe, D. J. J. Am. Chem.
    Soc. 1977, 24, 7992.
    30. Taddei, F.; Maran, F. J. Am. Chem. Soc. 2003, 125,
    14905.
    31. Addison, A. W.; Burke, P. J.; Henrick, K.; Rao, T. N.;
    Sinnic, E. Inorg. Chem. 1983, 22, 3645.
    32. Murray, S. G..; Hartley, F. R. Chem. Rev. 1981, 81, 365.
    33. Dagdigian, J. V.; McKee, V.; Reed, C. A. Inorg. Chem.
    1982, 21, 1332.
    34. Vaidyanathan, M.; Balamurugan, R.; Sivagnanam, U.;
    Palaniandavar, A. J. Chem. Soc. Dalton Trans. 2001,
    3498.
    35. Dagdigian, J. V.; Reed, C. A. Inorg. Chem. 1979, 18,
    2623.
    36. Hendrickson, A. R.; Martin, R. L.; Rohde, N. M. Inorg.
    Chem. 1975, 14, 2980.
    37. Hendrickson, A. R.; Martin, R. L.; Rohde, N. M. Inorg.
    Chem. 1976, 15, 2115.
    38. Hendrickson, A. R.; Martin, R. L.; Rohde, N. M. Inorg.
    Chem. 1974, 13, 1933.
    39. Hendrickson, A. R.; Martin, R. L.; Rohde, N. M. Inorg.
    Chem. 1975, 14, 1894.
    40. Gagné, R. R.; Allison, J. L.; Gall, R. S.; Koval, C. A.
    J. Am. Chem. Soc. 1977, 22, 7170.
    41. Percec, V.; Popov, A. V.; Ramirez-Castillo, E.;
    Monteiro, M.; Barboiu, B.;Weichold, O.; Asandei, A. D.;
    Mitchell, C. M. J. Am. Chem. Soc. 2002, 124, 4940.
    42. Tomaszewski, L.; Lagger, G..; Girault, H. H. Anal.
    Chem. 1999, 71, 837.
    43. Lippard, S. J.; Kuzelka, J.; Mukhopadhyay, S.;
    Spingler, B. Inorg. Chem. 2004, 43, 1751.
    44. Tolman, W. B.; Schneider, J. L.; Carrier, S. M.;
    Ruggiero, C. E.; Young JR., V. G. J. Am. Chem. Soc.
    1998, 120, 11408.
    45. Reedijk, J.; van Albada, G. A.; Smeets, W. J. J.; Spek,
    A. L. Inorg. Chim. Acta 1997, 151.
    46. Casella, L.; Battaini, G.; Gullotti, M.; Monzani, E.;
    Nardin, G.; Perotti, A.; Randaccio, L.; Santagostini,
    L.; Heinemann, F. W.; Schindler, S. Eur. J. Inorg.Chem.
    2003,1197.
    47. Kaim,W.; Albrecht, M.; Hü1bler, K.; Zalis, S. Inorg.
    Chem. 2000, 39, 4731.
    48. Miskowski, V. M.; Schugar, H. J.; Thich, J. A.;
    Solomon, R. J. Am. Che. Soc. 1976, 98, 8344.
    49. Bosnich, B.; Downes, J. M.; Whelan, J. Inorg. Chem.
    1981, 20, 1081.
    50. Fabbrizzi, L.; Lari, A.; Poggi, A.; Seghi, B. Inorg.
    Chem., 1982, 21, 2083.
    51. Schugar, H. J.; Potenza, J. A.; Fawcett, T. G.; Rudich,
    S. M.; Hughey, J. L.; Lalancette,R. A. J. Am. Chem.
    Soc. 1979, 2617.
    52. Addison, A. W.; Sinn, E. Inorg. Chem, 1983, 22, 1225.
    53. Anderson, O. P.; Perkins, C. M.; Brito, K. K. Inorg.
    Chem, 1983, 22, 1267.
    54. Tolman, W. B.; Hill, L. M. R.; Gherman, B. F.;
    Aboelella, N. W.; Cramer, C. J. Dalton Trans. 2006,
    4944.
    55. Fujisawa, K.; Lehnert, N.; Ono, T.; Ishikawa, Y.; Amir,
    N.; Miyashita, Y.; Okamoto K. Inorg. Chem. 2006, 45,
    1698.
    56. Yam, V. W. W.; Lam, C. H.; Fung, K. M.; Cheung, K. K.
    Inorg. Chem. 2001, 40, 3435.
    57. Dance, I. G. Polyhedron 1986, 2, 1031.
    58. Dance, I. G. Polyhedron 1986, 5, 1037.
    59. Dance, I. G.; Bowmaker, G. A.; Clark, G. R.; Seadon, J.
    K. Polyhedron 1983, 2, 1031.
    60. Healy, P. C.; Bott, R. C.; Sagatys, D. S. Chem. Commun.
    1998, 2403.
    61. Dance, I. G. ; Guerney, P. J.; Rae, A. D.; Scudder, M.
    L. Inorg. Chem. 1983, 22, 2883.
    62. Nakamura, A.; Okamura, T.; Ueyama, N.; Ainscough, E.
    W.; Brodie, A. M.; Waters, J. M. J. Chem. Soc. Chem.
    Commun., 1993, 1658.
    63. Vittal, J. J.; Lai, G. X.; Deivaraj, T. C. Inorg. Chem,
    2000, 39, 1028.
    64. Gunnoe, T. B.; Delp, S. A.; Munro-Leighton, C.; Goj, L.
    A. ; Ramírez, M. A.; Petersen, J. L.; Boyle, P. Inorg.
    Chem. 2007, 46, 2365.

    無法下載圖示 本全文未授權公開
    QR CODE