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/123456789/35362
完整後設資料紀錄
DC 欄位值語言
dc.contributor.advisor陳竹亭(Jwu-Ting Chen)
dc.contributor.authorHui-Ju Yuen
dc.contributor.author游蕙如zh_TW
dc.date.accessioned2021-06-13T06:49:38Z-
dc.date.available2015-07-27
dc.date.copyright2011-07-27
dc.date.issued2011
dc.date.submitted2011-07-22
dc.identifier.citation1. Lippard, S. J.; Berg, J. M. Principles of bioinorganic chemistry; University Science Books, 1994.
2. Cowan, J. A. Inorganic Biochemistry:An Introduction; VCH Publishers: New York, 1997.
3. Willams, D. R. Chem. Rev., 1972, 72 (3), 203-213.
4. Bertini, I.; Gray. H. B.; Stiefel, E. I.; Valentine, J. S. Biological inorganic chemistry:structure and reactivity; University Science Books, Sausalito, CA 2006.
5. Koval, I. A.; Gamez, P.; Belle, C.; Selmeczi, K.; Reedijk, J. Chem. Soc. Rev. 2006, 35, 814-840.
6. Holm, R. H.; Kennepohl, P.; Solomon, E. I. Chem. Rev. 1996, 96, 2239-2314.
7. Mirica, L. M.; Ottenwaelder, X.; Stack, T. D. P. Chem. Rev. 2004, 104, 1013-1045.
8. Kaim, W.; Rall, J. Angew. Chem., Int. Ed. Engl. 1996, 35, 43-60.
9. Whittaker, M. M.; Whittaker, J.W. Biophys. J. 1993, 64, 762-772.
10. Klinman, J. P. Chem Rev. 1996, 96, 2541-2562.
11. Ito, N.; Philips, S. E. V.; Stevens, C.; Ogel, Z. B.; McPherson, M. J.; Keen, J. N.; Yadav, K. D. S.; Knowles, P. F. Nature. 1991, 350, 87–90.
12. Mahadevan, V.; Gebbink, RJM. K.; Stack, T. D. P. Curr. Opin. Chem. Bio. 2000, 4, 228-234.
13. Humphreys, K. J.; Mirica, L. M.; Wang, Y.; Klinman, J. P. J. AM. CHEM. SOC. 2009, 131, 4657-4663.
14. (a) Goldberg, D. P.; Lippard, S. J. Adv. Chem. Ser. 1995, 246, 61-81. (b) Chaudhuri, P.; Wieghardt, K. Prog. Inorg. Chem. 2001, 50, 151-216. (c) Jazdzewski, B. A.; Tolman, W. B. Coord. Chem. Rev. 2000, 200-202, 633-685. (d) Itoh, S.; Taki, M.; Fukuzumi, S. Coord. Chem. Rev. 2000, 198, 3-20.
15. Thomas, F. Eur. J. Inorg. Chem. 2007, 2379-2404.
16. Karlin, K. D.; Gan, Q. F.; Farooq, A.; Liu, S.; Zubieta, J. Inorg. Chem. 1990, 29, 2549-2551.
17. Chaudhuri, U. P.; Whiteaker, L. R.; Yang, L.; Houser, R. P. Dalton Trans. 2006, 1902-1908.
18. Mukherjeea, P.; Drewb, M. G. B.; Estraderc, M.; Diazc, C.; Ghosh, A. Inorganica Chimica Acta. 2008, 361, 161-172.
19. Roth, A.; Becher, j.; Herrmann, C.; Gorls, H.; Vaughan, G.; Reiher, M.; Klemm, D.; Plass, W. Inorg. Chem. 2006, 45, 10066-10076.
20. Singh, K.; Long, J. R.; tavropoulos, P. Inorg. Chem. 1998, 37, 1073-1079.
21. Roy, P.; Manassero, M. Dalton Trans. 2010, 39, 1539-1545.
22. Contaldi, S.; Nicola, C. D.; Garau, F.; Karabach, Y. Y.; Martins, M.D.R.S.; Monari, M.; Pandolfo, L.; Pettinari, C.; Pombeiro, A. J. L. Dalton Trans. 2009, 4928-4941.
23. Brown, E.C.; Johnson, B.; Palavicini, S.; Kucera, B. E.; Casella, L.; Tolman, W. B. Dalton Trans., 2007, 3035-3042.
24. Biswas, C.; Drew, M. G. B.; Ruiz, E.; Estrader, M.; Diaz, C.; Ghosh, A. Dalton Trans., 2010, 39, 7474-7484.
25. Henkelis, J. J.; Jones, L. F.; Miranda, M. P.; Kilner, C. A.; Halcrow, M. A. Inorg. Chem. 2010, 49, 11127-11132.
26. Mukherjee, S.; Mukherjee, P. S. Inorg. Chem. 2010, 49, 10658–10667.
27. (a) Monzani, E.; Casella, L.; Zoppellaro, G.; Gullotti, M.; Pagliarin, R.; Bonomo, R. P.; Tabbì, G.; Nardin, G.; Randaccio, L. Inorg. Chim. Acta. 1998, 282, 180-192. (b) Mimmi, M. C.; Gullotti, M.; Santagostini, L.; Saladino, A.; Casella, L.; Monzani, E.; Pagliarin, R. Journal of Molecular Catalysis A. 2003, 204-205, 381-389. (c) Mimmi, M. C.; Gullotti, M.; Santagostini, L.; Battaini, G.; Monzani, E.; Pagliarin, R.; Zoppellarod, G.; Casella, L. Dalton Trans. 2004, 14, 2192-2201. (d) Mutti, F. G.; Pievo, R.; Sgobba, M.; Gullotti, M.; Santagostini, L. Bioinorg Chem Appl. 2008, 762029.
28. (a) Chen, P. P.-Y.; Yang, R. B.-G.; Lee, J. C.-M.; Chan, S. I. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 14570-14575. (b) Chan, S. I.; Yu, S. S.-F. Acc. Chem. Res. 2008, 41(8), 969-979.
29. Rotthaus, O.; Jarjayes, O.; Philouze, C.; Del Valle, C. P.; Thomas, F. Dalton Trans. 2009, 1792-1800.
30. Glaser, T.; Heidemeier, M.; Fröhlich, R.; Hildebrandt, P.; Bothe, E.; Bill, E. Inorg. Chem. 2005, 44, 5467-5482.
31. Chaudhuri, S. K.; Roy, S.; Saha, M.; Bhar, S. Synthetic Comm. 2007, 37, 581-585.
32. Hansen, T. V.; Skattebøl, L. Tetrahedron Let. 2005, 46, 3829-3830.
33. Görl, C.; Alt, H.G. J. Organometallic Chem. 2007, 692, 5727-5753.
34. Pavia, D. L.; Lampman, G. M.; Kriz, G. S. Introduction to Spectroscopy, Brooks/Cole, 2000.
35. Lui, F.-Y. master thesis, 2010, 52-53.
36. Bharathi, K. S.; Sreedaran, S.; Rahiman, A. K.; Rajesh, K.; Narayanan, V. Polyhedron. 2007, 26, 3993-4002.
37. Shakya, R.; Imbert, C.; Hratchian, H. P.; Lanznaster, M.; Heeg, M. J.; McGarvey, B. R.; Allard, M.; Schlegel, H. B.; Veran, C. N. Dalton Trans. 2006, 2517-2525.
38. Yin, H. Acta Cryst. 2008, C64, m324-m326.
39. Geary, W. J. Coord. Chem. Rev. 1971, 7, 81-122.
40. (a) Dutta, G.; Debnath, R. K.; Kalita, A.; Kumar, P.; Sarma, M.; Shankar, R. B.; Mondal, B. Polyhedron. 2011, 30, 293-298. (b) Pradeep, C. P.; Zacharias, P. S.; Das, S. K. J. Chem. Sci. 2005, 117, 133-137. (c) Halcrow, M. A.; Chia, L. M. L.; Liu, X.; McInnes, E. J. L.; Yellowlees, L. J.; Mabbs, F. E.; Scowen, I. J.; McPartlin, M.; Davies, J. E. J. Chem. Soc., Dalton Trans. 1999, 1753-1762.
41. (a) Halfen, J. A.; Jazdzewski, B. A.; Mahapatra, S.; Berreau, L. M.; Wilkinson, E. C.; Jr., L. Q.; Tolman, W. B. J. Am. Chem. Soc. 1997, 119, 8217-8227. (b) Gamez, P.; Koval, I. A.; Reedijk, J. Dalton Trans. 2004, 4079-4088.
42. Browni, J. C.; Wardeska, J. G. Inorg. Chem. 1982, 21, 1530-1534.
43. (a) Du, W. –X.; Zhang, J. –J.; Hu, S. –M.; Xia, S. –Q,; Fu, R. –B.; Xiang, S. –C.; Li, Y. –M.; Wang, L. –S.; Wu, X. –T. J. Mol. Struct. 2004, 701, 25-30. (b) Guerriero, P.; Casellato, U.; Ajo, D.; Sitran, S.; Vigato, P. A.; Graziani R. Inorg. Chim. Acta. 1988, 142, 305-313. (c) Motekaitis, R. J.; Rudolf, P. R.; Martell, A. E.; Clearfield, A. Inorg. Chem. 1989, 28, 112-115. (d) Dalley, N. K.; Xue, G.; Bradshaw, J. S.; Zhang, X. X.; Harrison, R. G.; Savage, P. B.; Krakowiak, K. E.; Izatt, R. M. J. Heterocycl. Chem. 2001, 38, 1.
44. Addison, A. W.; Rao, T. N.; Reedijk, J.; Van Rijn, J.; Verschoor, G. C. J. Chem. Soc., Dalton Trans. 1984, 1349-1356.
45. (a) Diez, J.; Gamasa, M. P.; Gimeno, J.; Aguirre, A.; Garda-Granda, S. Organometallics, 1991, 10, 380–382. (b) Diez, J.; Gamasa, M. P.; Gimeno, J. Polyhedron, 1995, 14, 741–745. (c) Bera, J. K.; Nethaji, M.; Samuelson, A. G. Inorg. Chem. 1999, 38, 218-228. (d) Boca, R.; Dlhan, L.; Mezei, G.; Ortiz-Perez, Tamara; Raptis, R. G.; Telser, J. Inorg. Chem. 2003, 42, 5801−5803. (e) Kohn, R. D.; Laudo, L. T.; Pan, Z.; Speiser, F.; Kociok-Kohn, G. Dalton Trans. 2009, 4556–4568 (f) Wang, L.-L.; Sun, Y.-M.; Yu, Z.-Y.; Qi, Z.-N.; Liu, C.-B. J. Phys. Chem. A. 2009, 113, 10534–10539. (g) Andrés-Tomé, I.; Winscom, C. J.; Coppo, P. Eur. J. Inorg. Chem. 2010, 23, 3567–3570. (h) Tsui, E. Y.; Day, M. W.; Agapie, T. Angew. Chem. 2011, 123, 1706–1710.
46. (a) Du, M.; Zhao, X.J.; Guo, J.H.; Bu, X. H.; Ribas, J. Eur. J. Inorg. Chem. 2005, 294-304. (b) Kahn, O. Molecular Magnetism; VCH: Weinheim, Germany, 1993. (c) Song, Y.; Gamez, P.; Roubeau, O.; Mutikainen, I.; Turpeinen, U.; Reedijk, J. Inorganica Chimica Acta. 2005, 358, 109-115.
47. (a) Gautier-Luneau, I.; Phanon, D.; Duboc, C.; Luneau, D.; Pierre, J, -L. Dalton Trans. 2005, 3795-3799. (b) Figgis, B. N.; Martin, D. J. J. Chem. Soc. Dalton Trans. 1972, 2174-2176.
48. Crawford, V. H.; Richardson, H.W.; Wasson, J. R.; Hodgson, D. J.; Hatfield, W. E. Inorg. Chem. 1976, 15, 2107-2110.
49. (a) Hulsbergen, F. B.; Hoedt, R. W. M.; Verschoor, G. C.; Rdijk, J.; Spck, A. L. J. Chem. Soc., Dalton Trans. 1983, 539-545. (b) Arora, H.; Philouze, C.; Jarjayes, O.; Thomas, F. Dalton Trans. 2010, 39, 10088-10098. (c) Dasgupta, S.; Khatua, S.; Bertolasi, V.; Bhattacharjee, M. Polyhedron. 2007, 26, 2574–2580. (d) Schatz, M.; Becker, M.; Thaler, F.; Hampel, F.; Schindler, S.; Jacobson, R. R.; Tyeklár, Z.; Murthy, N. N.; Ghosh, P.; Chen, Q.; Zubieta, J.; Karlin, K. D. Inorg. Chem. 2001, 40, 2312-2322.
50. Drago, R.S., Physical Methods for Chemists, 2nd ed.; Saunders College: Orlando, FL, 1992.
51. (a) Safaei, E.; Kabir, M. M.; Wojtczak, A.; Jagličić, Z.; Kozakiewicz, A.; Lee, Y, -I. Inorganica Chimica Acta. 2011, 366, 275-282. (b) Arion, V. B.; Rapta, P.; Telser, J.; Shova, S. S.; Breza, M.; Lušpai, K.; Kožišek, J. Inorg. Chem. 2011, 2918-2931. (c) Thomas, F.; Jarjayes, O.; Duboc, C.; Philouze, C.; Saint-Aman, E.; Pierre, J, -L. Dalton Trans. 2006, 2662-2669.
52. (a) Deunf, E.; Zaborova, E,; Guieu, S.; Blériot, Y.; Verpeaux, J, -N.; Buriez, O.; Sollogoub, M.; Amatore, C. Eur. J. Inorg. Chem. 2010, 4720-4727. (b) Safaei, E.; Wojtczak, A.; Bill, E.; Hamidi, H. Polyhedron. 2010, 29, 2769-2775. (c) Tas, E.; Kilic, A.; Durgun, M.; Küpecik, L.; Yilmaz, I.; Arslan, S. Spectrochimica Acta Part A. 2010, 75, 811-818. (d) Neves, A. P.; Maia, K. C.B.; Vargas, M. D.; Visentin, L. C.; Casellato, A. Polyhedron. 2010, 29, 2884-2891.
53. (a) Maloth, S.; Pal, S. Polyhedron. 2010, 29, 3257-3261. (b) Rybak-Akimova, E. V.; Nazarenko, A. Y.; Chen, L.; Krieger, P. W.; Herrera, A. M.; Tarasov, V. V.; Robinson, P. D. Inorganica Chimica Acta. 2001, 324, 1-15. (c) Pereira, E.; Gomes, L. R.; Low, J. N.; Castro, B. D. Polyhedron. 2008, 27, 335-343. (d) Mukhopadhyay,S.; Mandal, D.; Chatterjee, P. B.; Desplanches, C. D.; Sutter, J-P.; Butcher, R. J.; Chaudhury, M. Inorg. Chem. 2004, 43, 8501-8509.
54. (a) Muppidi, V. K.; Zacharias, P. S.; Pal, S. Chem. Commun. 2005, 19, 2515-2517. (b) Muppidi, V. K.; Das, S.; Raghavaiah, P.; Pal, S. Inorg Chem Comm. 2007, 10, 234-238.
55. Wolsey, W. C. J. Chem. Educ. 1973, 50, A335-A337.
dc.identifier.urihttp://tdr.lib.ntu.edu.tw/jspui/handle/123456789/35362-
dc.description.abstract自然界中的金屬蛋白催化許多生物體中氧化還原反應,其主要的活性中心通常都為多金屬離子作為輔因子,而生物體中含量豐富的銅離子在許多生理功能上扮演非常重要的角色。研究金屬蛋白的化學反應機制,因受限於蛋白質結構的折疊及活性離子的不穩定性,使得生物無機化學家企圖以合成模型化合物的方式來探討其活性中心的結構與其反應機制。
本篇論文主要為合成含氨基-酚及雙胺-雙醇官能基的N4O4八牙之配位基(L-6/7-PhRX)並與銅離子形成多銅錯合物,藉以來了解探討其配位基與銅離子之間的配位模式和其衍生的物理化學性質。藉由反應物中銅離子當量數的調控,可以得到三銅或七銅錯合物,以紅外光共振光譜(IR) 、紫外光-可見光光譜(UV-Vis)、電噴灑質譜儀(ESI-MS)、導電度測量(conductivity measurement)、電子自旋共振光譜(EPR)、超導量子干涉磁化儀(SQUID)、循環伏安電儀(Cyclic voltammogram)與元素分析儀(elemental analysis),了解其分子結構的組成並對於其物理性質加以探討。
不同幾何形狀的三銅、七銅晶體皆由 X光單晶繞射解析出來,藉由紫外光-可見光光譜和導電度測量,可以得知,七銅錯合物由多餘的銅離子連接兩個三銅錯合物在晶體堆疊時形成,而當其溶於液體時會自解離成三銅錯合物。由電子自旋共振光譜及超導量子干涉磁化儀結果顯示,此類藉由氧原子做為架橋的三銅錯合物具有明顯的反鐵磁現象(antiferromagnetic coupling)。最後,利用循環伏安法可以測得此八配子配位基具有氧化的能力,因此可以利用此新式八配子配位基來探討生物體中含銅金屬蛋白中心對於單電子氧化的情形。
zh_TW
dc.description.abstractMetalloproteins containing multi-copper centers as catalytically active site are usually involved in several major biological oxidation-reduction reactions. Thus multinuclear copper complexes have motivated many inorganic chemists to attempt to develop the synthesis as well as investigate coordination chemistry of such species.
In this work, new multinuclear network of CuII ions with octadentate N4O4-ligands, specifically containing the combination of amino-phenoxide and diamine-dialkoxide components (L-6/7-PhRX) have been successfully synthesized and structurally characterized. The ligands are mainly characterized by NMR techniques. Furthermore, the inorganic species are examined by conductivity measurements, ESI-Mass, UV-Vis, IR, EPR, and CV. A few examples were confirmed by X-ray diffractions. Single crystals of the tricopper complexes and the unusual dimeric compounds were obtained by modulating the number of copper equivalent. The latter heptacopper complexes were dimerized from two tricopper(II) species which were interacted with an extra CuII ions by our phenolate and two bridged hydroxylate oxygens.
en
dc.description.provenanceMade available in DSpace on 2021-06-13T06:49:38Z (GMT). No. of bitstreams: 1
ntu-100-R98223215-1.pdf: 11648178 bytes, checksum: 16ae5ec49ce6797c87d156197b2fb7cd (MD5)
Previous issue date: 2011
en
dc.description.tableofcontentsChapter 1 Introduction 1
1-1 Introduction to Metalloenzymes 1
1-2 Overview of the Copper Proteins 4
1-3 Tyrosine Ligand Contained Copper Metalloenzymes 8
1-3-1 Galactose Oxidase 8
1-4 Multinuclear copper complexes 11
1-5 Octadentate Ligand Design 13
Chapter 2 Ligand Synthesis and Characterization 16
2-1 Synthesis Aspect of Octadentate Ligands 16
2-2 Synthesis of Bidentate Ligands 17
2-2-1 Amino-Phenoxide Ligand Synthesis 17
2-3 Synthesis of Octadentate Ligands 23
2-3-1 Symmetrical Synthesis Pathway 23
2-3-2 Unsymmetrical Synthesis Pathway 34
Chapter 3 Copper(II) Complexes Synthesis and Characterization 45
3-1 Copper(II) Complexes Synthesis 45
3-1-1 Scan for Expirimental Condition 45
3-2 Tricopper(II) Complexes Synthesis 50
3-3 Monocopper(II) Complexes Synthesis 52
3-4 Scaning Copper(II) Sources as Starting Meterials 53
3-5 Characterization of Tricopper(II) Complexes 54
3-5-1 Infrared Spectroscopy 54
3-5-2 ESI-MS and HR-ESI-MS 56
3-5-3 Conductivity Measurement 60
3-5-4 UV-Vis spectra of Copper(II) Complexes 64
3-6 Crystal Structures of the Multicopper(II) Complexes 66
3-7 Physisal Properties Measurement 76
3-7-1 Magnetic Properties 76
3-7-2 Electron paramagnetic resonance (EPR) spectroscopy
80
3-8 Elemental Analysis 83
3-9 Cyclic voltammograms 83
3-10 Characterization of Monocopper(II) Complexes 86
3-10-1 ESI-MS and HR-ESI-MS 86
3-10-2 UV-Vis spectra of Copper(II) Complexes 88
3-10-3 EPR spectroscopy
88
3-11 Using Other Metal Ions To Investigate Coordination Mode of Octadentate Ligands 89
3-11-1 FeIII Complexes 90
3-11-2 NiII Complexes 91
Chapter 4 Conclusions 94
Chapter 5 Experimental Section 97
Chapter 6 Renference 128
Appendix 136
dc.language.isoen
dc.subject多銅(II)金屬錯合物zh_TW
dc.subject八牙配位基zh_TW
dc.subjectMultidentate Ligandsen
dc.subjectMulti-copper(II) Complexesen
dc.title含N4O4八牙配位基之合成及其多銅(II)金屬錯合物合成與結構鑑定之研究zh_TW
dc.titleSynthesis and Structures of Multi-copper(II) Framework Containing N4O4-Multidentate Ligandsen
dc.typeThesis
dc.date.schoolyear99-2
dc.description.degree碩士
dc.contributor.oralexamcommittee王瑜,張啟光,葉鎮宇
dc.subject.keyword八牙配位基,多銅(II)金屬錯合物,zh_TW
dc.subject.keywordMulti-copper(II) Complexes,Multidentate Ligands,en
dc.relation.page174
dc.rights.note有償授權
dc.date.accepted2011-07-25
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-100-1.pdf
  未授權公開取用
11.38 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