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研究生: 蔡懿宣
Tsai, Yi-Hsuan
論文名稱: 三價錳氫氧及過氧烷錯合物之鑑定與反應性
Characterization and Reactivity of Mn(III)-Hydroxo and -Alkylperoxo Complexes
指導教授: 李位仁
Lee, Way-Zen
學位類別: 碩士
Master
系所名稱: 化學系
Department of Chemistry
論文出版年: 2019
畢業學年度: 107
語文別: 中文
論文頁數: 48
中文關鍵詞: 含錳-氧合酶四價錳氫氧錯合物四價錳過氧烷錯合物
英文關鍵詞: Mn enzymes, Mn(IV)-Hydroxo, Mn(IV)-Alkylperoxo complex
DOI URL: http://doi.org/10.6345/NTNU201900402
論文種類: 學術論文
相關次數: 點閱:43下載:0
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  • 在許多的含錳酵素催化循環中,高價態錳氧錯合物與錳的過氧烷錯合物被認為是可能存在的反應中間物,特別是第二光系統(Photosystem II)中的氧釋放複合體(Oxygen-Evolving Complex)、含錳雙加氧酶(Manganese-Dependent Dioxygenase)和含錳脂氧合酶(Mn-Lipoxygenase),為了能模擬這些在酵素反應中的中間物,本研究利用實驗室所開發的三價錳錯合物:[MnIIIBDPP(H2O)]PF6 (2)、MnIIIBDPP(OH) (5)。錯合物(2)可以透過氧化劑Magic Blue (Tris(4-bromophenyl) aminium hexachlorido antimonate)氧化成錯合物(6),再加入有機鹼DBU會反應成錯合物(7),推測錯合物(6)與(7)分別為[MnIVBDPP(H2O)]2+和[MnIVBDPP(OH)]+,也透過UV-vis光譜和EPR光譜來鑑定為高自旋四價錳錯合物(S = 3/2),還利用苯酚衍生物證實錯合物(7)能作氫原子轉移。錯合物(5)加入cumene hydroperoxide後形成錯合物(8),還可以透過Magic Blue氧化形成錯合物(9),推測錯合物(8)、(9)為MnIIIBDPP(OOCm)和[MnIVBDPP(OOCm)]+,以UV-vis光譜和EPR光譜來鑑定為高自旋四價錳錯合物(S = 3/2),同時利用2-PPA作O-O鍵裂解,也利用1,4-CHD作C-H鍵活化。

    High valent manganese oxygen species and manganese alkylperoxo are proposed intermediates in the catalytic cycles of most manganese containing enzymes, especially for Oxygen-Evolving Complex in Photosystem II, Manganese-Dependent Dioxygenase, and Mn-Lipoxygenase. In order to simulate these intermediates, this study utilizes a serial of MnIIIBDPP complexes developed by our laboratory : [MnIIIBDPP(H2O)]PF6 (2), MnIIIBDPP(OH) (5), were prepared. (2) can be oxidized to (6) by an oxidant as Magic Blue (Tris(4-bromophenyl) aminium hexachlorido antimonate), and then the organic base DBU is added to react into (7). (6) and (7) are speculated [MnIVBDPP(H2O)]2+ and [MnIVBDPP(OH)]+ when we identified as high-spin quaternary manganese complex by UV-vis spectroscopy and EPR spectroscopy (S = 3/ 2). We also used phenol derivatives to confirm that (7) can do HAT. We added cumene hydroperoxide (5) to form (8), and added Magic Blue to oxidize (8) to (9). We assumed that (8) and (9) are MnIIIBDPP(OOCm)and [MnIVBDPP(OOCm)]+ respectively. UV-vis spectroscopy and EPR spectroscopy were used to identify high-spin quaternary manganese complexes (S = 3/2), while 2-PPA was used for O-O bond cleavage, and 1,4-CHD was also used for C-H bond activation.

    目錄 I 圖索引 III 中文摘要 VI Abstract VII 第一章 緒論 1 1-1 光系統II中的錳金屬與氧 2 1-2 自然界中含鐵與含錳金屬的蛋白及酶 3 1-3 錳金屬羥基錯合物(Manganese-Hydroxo Complexes) 7 1-4 錳過氧烷錯合物(Manganese-Alkylperoxo Complexes) 12 第二章 實驗部分 15 2-1 實驗藥品 15 2-2 實驗儀器及條件 16 2-3 錳系列錯合物之合成與鑑定 20 第三章 結果與討論 22 3-1 錳系列錯合物之合成 22 3-2 錯合物MnIIIBDPP(OH) (5)之製程探討 28 3-3 錯合物MnIIIBDPP(OH) (5)氧化後之反應性探討 30 3-4 錯合物MnIIIBDPP(OH) (5)與Cumene hydroperoxide反應探討 35 3-5 錯合物(8)與錯合物(9)之反應性探討 39 第四章 結論與展望 44 參考文獻 46 附錄A X-ray單晶繞射解析結構及晶體常數 48

    1. 2013, 朱其翊學長碩士論文
    2. Kamiya, N.; Kawakami, K.; Umena, Y. Nature 2011, 473, 55–60.
    3. Noguchi, T. J. Am. Chem. Soc. 2017, 139, 2022−2029
    4. Cox, N.; Lubitz, W. Science. 2014, 345, 804–808
    5. Allakhverdiev, S. I.; Najafpour, M. M. Chem. Rev. 2016, 116, 2888–2936
    6. Pollock, C. J.; Silakov, A.; Krebs ,C; Bollinger, J. M., Jr J. Am. Chem. Soc. 2017, 139, 1950–1957
    7. Oliw, E. H.; Karkehabadi, S. J. Biol. Chem., 2016, 291, 8130–8139
    8. Valentine, J. S.; Teixeira, M.; Miller, A. F.; Maroney, M. J.; Cabelli, D. E.;Abreu, I. A. Chem. Rev. 2014, 114, 3854–3918
    9. Fujii, H. Inorg. Chem. 2010, 49, 6664–6672
    10. Fujii, H. Inorg. Chem. 2008, 47, 1674–1686
    11. Borovik, A. S.;Hendrich, M. P.; Yano, J. Chem. Sci., 2014, 5, 3064–3071
    12. Borovik, A. S.; Hendrich, M. P. Inorg. Chem. 2013, 52, 12568–12575
    13. Busch, D. H. J. Am. Chem. Soc. 2008, 130, 16245–16253
    14. Jackson, T. A. Inorg. Chem. 2016, 55, 3272–3282
    15. Stack, T. D. P. J. Am. Chem. Soc. 2005, 127, 9904–9912
    16. Borovik, A. S. J. Am. Chem. Soc. 2003, 125, 13234–13242
    17. Kovas, J. A. Inorg. Chem. 2013, 52, 12383–12393
    18. Jackson, T. A. Inorg. Chem. 2014, 53, 7622–7634
    19. Jackson, T. A. Inorg. Chem. 2016, 55, 8110−8120
    20. McDonald, A. R. J. Am. Chem. Soc. 2016, 138, 14362–14370
    21. Goldberg, D. P. J. Am. Chem. Soc. 2012, 134, 16619–16634
    22. Que, L., Jr.; Farquhar, E. R.; Emerson, J. P. PNAS., 2008, 105, 7347–7352
    23. Lee, W.-Z.; Münck, E.; Que, L., Jr.; Bominaar, E. L. J. Am. Chem. Soc., 2014, 136, 10846–10849
    24. Lee, W.-Z.; Liaw, W.-F.; Tasi, M.-L.; Ye, S.-F. J. Am. Chem. Soc., 2016, 138, 14186–14189
    25. Fukuzumi, S.; Nam, W. J. Am. Chem. Soc. 2018, 140, 12695−12699
    26. Goldberg, D. P. J. Am. Chem. Soc. 2018, 140, 4380−4390
    27. Anderson, J. S. J. Am. Chem. Soc. 2018, 140, 13176−13180
    28. Richards, N. G. J. Essays. Biochem. 2017, 61, 259-270
    29. Bornemann. S. Biochem. J. 2007, 407, 397-406
    30. Brudvig. G. W. Photochem. Photobiol. Sci. , 2005, 4 , 940–949
    31. Neese. F.; Ye, S.-F. Chem. Sci., 2012, 3, 1600–1611
    32. Mascharak. P. K. J. Am. Chem. Soc. 1998, 120, 9015-9027
    33. Itoh. S. J. Am. Chem. Soc. 2008, 130, 4244-4245
    34. Kovacs. J. A. J. Am. Chem. Soc. 2013, 135, 4260-4272
    35. Cho. J. Chem. Commun., 2017, 53, 9328--9331

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