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  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/123456789/23474
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DC 欄位值語言
dc.contributor.advisor陳竹亭
dc.contributor.authorFeng-Yu Liuen
dc.contributor.author劉豐瑜zh_TW
dc.date.accessioned2021-06-08T05:02:10Z-
dc.date.copyright2010-08-24
dc.date.issued2010
dc.date.submitted2010-08-20
dc.identifier.citation1. Jiang, h.; Chen, Y.; Jiang, P.; Zhang, C.; Smith, T. J.; Murrell, J. C.; Xing, X. H., J. Biochem. Engin., 2010, 49, 277–288
2. (a) Hanson, R. S.; Hanson, T. E., Microbio. Rev., 1996, 60, 439-471.(b) Lieberman, R.L.; Amy C. R., Nature, 2005, 434, 177-182
3. (a) Yoshizawa, K.; Suzuki, A.; Shiota, Y.; Yamabe, T., Bull. Chem. Soc. Jpn., 2000, 73, 815-827. (b) Yoshizawa, K. J., Inorg. Biochem., 2000, 78, 23-34. (c) Valentine, A. M.; Wilkinson, B.; Liu, K. E.; Komar-Panicucci, S.; Priestley, N.D.; Willoams, P. G.; Morimoto, H.; Floss, H. G.; Lippard, S. J., J. Am. Chem. Soc., 1997, 119, 1818-1827 (d) Wilkinson, B.; Zhu, M.; Priestley, N. D.; Nguyen, H. H. T.; Morimoto, H.; Williams, P. G.; Chan, S. I.; Floss, H. G., J. Am. Chem. Soc., 1996, 118, 921-922.
4. (a) Valentitine, A. M.; LeTadic-Biadatti, M.-H.; Toy, P. H.; Newcomb, M.; Lippard, S. J., J. Biol. Chem., 1999, 274, 10771-10776. (b) Lipscomb, J. D., Biochemistry, 1996, 35, 10240-10247.
5. (a) Chen, P. P. Y.; Yang, R. B. G.; Lee, J. C. M; Chan, S. I., Proc. Natl. Acad. Sci., 2007, 104, 14570-14575 (b) Feig, A. L.; Lippard, S. J., Chem. Rev., 1994, 94, 759-805
6. (a) Nguyen, H. H. T.; Elliott, S. J.; Yip, J. H. K.; Chan, S. I., J. Biol. Chem., 1998, 273, 7957–7966. (b) Chen, K. H. C.; Yu, S. S. F.; chen, C.-L; Kuo, S. S., J. Biochemistry, 2004, 43, 4421-4430 (c) Semrau, J. D.; DiSpirito, A. A.; Yoon, S., Microbiol. Rev., 2010, 34, 496-531
7. Ramakrishnan B.; Amy C. R., Acc. Chem. Res. 2007, 40, 573-580
8. (a) Chan, S. I.; Steve S.-F. Yu Acc. Chem. Res., 2008, 41, 969-979
9. Chan, S. I.; Wang, V. C.-C.; Lai, J. C.-H.; Steve S.-F. Yu, Chen, P. P.-Y.; Chen, K. H.-C.; Chen, C.-L.; Chan, M. K., Angew. Chem. Int. Ed. 2007, 46, 1992–1994
10. (a) Lewis, E. A.; Tolman, W, B. Chem Rev., 2004, 104, 1047-1076 (b) Cole, A. P.; Root, D. E.; Mukherjee, p.; Solomon, E. L.; Stack, T. D. P., Science, 1996, 273, 1848-1850
11. Chen, P.P.Y.; Chan, S. I., J. Inorg. Biolchem., 2006, 100, 801-809
12. (a) Lieberman, R. L.; Rosenzweig, A. C., Dolton Trans, 2005 , 21, 3390 – 3396 (b) Lieberman, R. L.; Rosenzweig, A. C., Nature, 2005 , 434, 177 – 182
13. Chan, S. I.; Chen, K. H.-C.; Yu, S. S.-F.; Chen, C.-L.; Kuo, S. S.-J., Biochemistry, 2004, 43, 4421– 4430
14. Rosenzweig A. C., Bioche. Soc. Trans. 2008, 36, 1134-1137.
15. Santagostini, L.; Gullotti, M.; Pagliarin, R.; Bianchi, E.; Casella, L.; Monzani, E., Tetrahedron: Asymmetry, 1999, 10, 281-295
16. Santagostini, L.; Gullotti, M.; Pagliarin, R.; Monzani, E.; Casella, L., Chem. Commun. 2003, 2186–2187.
17. Santagostini, L.; Gullotti, M.; Pagliarin, R.; Monzani, E.; Casella, L.; Palavicini, S.; Zoppellaro, G., Eur. J. Inorg. Chem. 2008, 2081–2089
18. Messerschmidt, A.; Huber, R., Eur. J. Biochem., 1990, 187, 341-352
19. Mimmi, M. C.; Gullotti, M.; Santagostini, L.; Saladino, A.; Casella, L.; Monzani, E.; Pagliarin, R., J. Mol. Catal. A 2003, 204–205, 381–389
20. Mimmi, M. C.; Gullotti, M.; Santagostini, L.; Pagliarin, R.; Gioia, L. De.; Monzani, E.; Casella L., Eur. J. Inorg. Chem. 2003, 3934–3944
21. Mimmi, M. C.; Gullotti, M.; Santagostini, L.; Battaini, G.; Monzani, E.; Pagliarin, R.; Zoppellaro, G.; Casella, L., Dalton Trans. 2004, 2192–2201
22. Gullotti, M.; Santagostini, L.; Pagliarin, R.; Granata, A.; Casella, L., J. Mol. Catal. A 2005, 235, 271–284.
23. Chang, M.-C. master thesis, 2009 and some reference therein.
24. Roumen, L.; Peeters, J. W.; Emmen, J. M. A.; Beugels, I. P. E.; Custers, E. M. G.; Gooyer, M. D.; Plate, R.; Pieterse, K.; Hilbers, P. A. J.; Smits, J. F. M.; Vekemans, J. A. J.; Leysen, D.; Ottenheijm, H. C. J.; Janssen, H. M.; Hermans, J. J. R., J. Med. Chem., 2010, 53, 1712–1725
25. Gerber, T. I. A.; Tshentu, Z. R.; Mayer, P., J. Coord. Chem., 2003, 56, 1357–1366
26. Yang, Z.-C. master thesis, 2004 and some reference therein.
27. NguyenS, H.-H. T.; ShiemkeSP, K. S.; Jacobs, S. J.; Halesn, B. J.; Lidstromll, M. E.; Chan, S. I., J. Bio.Chem. 1994, 269, 14995-15005
28. Figgis, B. N.; Martin, D. J., J. Chem. Soc. Dalton Trans., 1972, 2174-2176
29. Isabelle, G.-L..; Phanon, D.; Duboc, C.; Luneau, D.; Pierre, J.-L., Dalton Trans, 2005, 3795-3799
30. Musie, G. T.; Li, X.; Powell, D. R., Inorg Chim Acta, 2003, 348, 69-74
31. Du, M.; Guo, Y.-M.; Chen, S.-T.; Bu, X.-H., J. Mole Stru, 2002, 641, 29-34
32. Bu, X.-H.; Du, M.; Shang, Z.-L.; Zhang, R.-H.; Liao, D.-Z.; Shionoya, M.; Clifford, T., Inorg. Chem. 2000, 39, 4190-4199
33. Tong, S. F.; Yang, H.; Lao, Y.-N.; Liu, G.-H.; Wu, H.-X.; Yang, S.P.; Yu, J.; Tan, H.; Li.W. Z., Anorg. Allg. Chem. 2009, 635, 2340–2346
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/23474-
dc.description.abstract甲烷氧化菌利用甲烷作為其主要的能源。甲烷單加氧酶微粒(pMMO)是一個鑲嵌在細胞膜上的含金屬酶,這個蛋白質可以催化甲烷變成甲醇。銅離子在pMMO的催化中心扮演重要的角色。因此我們成功的合成含有N6O2的八牙配位基並且鑑定此八牙配位基具有三個金屬配位的空間形成三銅錯合物。我們透過紅外光共振光譜儀(IR)、紫外光-可見光光譜(UV-Vis spectroscopy)、高解析電噴灑質譜儀(HR-ESI-MS)、元素分析(elemental analysis)、導電度測量(conductivity measurement)、電子自旋共振光譜(EPR)及超導量子干涉磁化儀(SQUID)鑑定包含此八牙配位基的三銅錯合物。我們可以確認三銅錯合物的化學式為〔(CuII)3(L)(μ-OH-)〕(ClO4-)3。zh_TW
dc.description.abstractMethanotrophic bacteria use methane as their primary source of energy and particulate methane monooxygenase (pMMO) is an integral membrane metalloenzyme that catalyses the conversion of methane to methanol. Copper plays a critical role in the active center of the pMMO enzymes. New tricopper (II) model derivatives of octadentate ligands of N6O2 combination for the donor atoms have been successfully synthesized, and the structure characterization of ligands contains three binding sites for copper (II) ions is studied. The tricopper (II) complexes with octadentate ligand have been characterized by infrared spectroscopy (IR), UV-Vis spectroscopy, HR-ESI-MS, elemental analysis, conductivity measurement, electron paramagnetic resonance (EPR) and SQUID. We could conclude the chemical formula of tricopper (II) complexes as 〔(CuII)3(L)(μ-OH-)〕(ClO4-)3.en
dc.description.provenanceMade available in DSpace on 2021-06-08T05:02:10Z (GMT). No. of bitstreams: 1
ntu-99-R97223204-1.pdf: 14026144 bytes, checksum: 804a99fd66c213feba8be0ed6dcdd3e1 (MD5)
Previous issue date: 2010
en
dc.description.tableofcontentsChapter 1 Introduction 1
1-1 Methane Monooxygenases (MMOs) 1
1-2 The Structure of pMMO and Tricopper in pMMO 4
1-3 Proposed Mechanism of Methane Oxidation Tricopper Cluster in pMMO 8
1-4 Octadentate Ligands Design 11
Chapter 2 Synthesis of Octadentate Ligands 15
2-1 Strategy for Octadentate Ligands Synthesis 15
2-2 Bidentate Ligand Synthesis 17
2-3 Synthesis and Characterization of the Octadentate Ligands 20
Chapter 3 Results and Discussions 28
3-1 Synthesis of the Tricopper (II) Complexes 28
3-1-1 The Role of Triethylamine for Synthesize the Tricopper (II) complexes 29
3-1-2 Synthesis of the Copper (II) Complexes in Different Solvent 32
3-2 Characterization of the Tricopper (II) Complexes 34
3-2-1 Infrared Spectroscopy 34
3-2-2 ESI-MS and HR-ESI-MS 35
3-2-3 Elemental Analysis 37
3-2-4 Conductivity Measurement 38
3-2-5 UV-Vis Spectra of Tricopper (II) Complexes 40
3-2-6 Physical Properties of the Tricopper (II) complexes 42
3-2-6(a) Electron Paramanetic Resonance (EPR) Spectra of the Tricopper (II) Compplexes 42
3-2-6(b) Magnetic Properties of the Tricopper (II) Complexes 42
3-3 Stoichiometry of the the Tricopper (II) Complexes Synthesis 46
3-3-1 Different Equivalents of Copper (II) Ions in the Tricopper (II) Complexes Synthesis 47
3-3-2 Synthesis of the Monopper (II) Complexes 52
3-4 Synthesis of the Tricopper (II) Complexes with Different Copper (II) Precursor 57
Chapter 4 Conclusions 58
Chapter 5 Experimental Section 59
Chapter 6 Reference 87
Appendix 91
dc.language.isoen
dc.title合成並鑑定含有N6O2八牙配位基之三銅(II)金屬錯合物zh_TW
dc.titleSynthesis and Characterization of the Tricopper (II) Complexes with Octadentate Ligand of N6O2 Combinationen
dc.typeThesis
dc.date.schoolyear98-2
dc.description.degree碩士
dc.contributor.oralexamcommittee許智能,鄭原忠
dc.subject.keyword八牙配位基,三銅錯合物,咪唑,zh_TW
dc.subject.keywordoctadentate ligand,tricopper (II) complexes,imidazole,en
dc.relation.page142
dc.rights.note未授權
dc.date.accepted2010-08-20
dc.contributor.author-college理學院zh_TW
dc.contributor.author-dept化學研究所zh_TW
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