English  |  正體中文  |  简体中文  |  Items with full text/Total items : 62570/95226 (66%)
Visitors : 2505011      Online Users : 58
RC Version 7.0 © Powered By DSPACE, MIT. Enhanced by NTU Library & TKU Library IR team.
Scope Tips:
  • please add "double quotation mark" for query phrases to get precise results
  • please goto advance search for comprehansive author search
  • Adv. Search
    HomeLoginUploadHelpAboutAdminister Goto mobile version
    Please use this identifier to cite or link to this item: https://tkuir.lib.tku.edu.tw/dspace/handle/987654321/97584

    Title: Photochemistry of the Dinitrosyl Iron Complex [S5Fe(NO)2]- Leading to Reversible Formation of [S5Fe(μ-S)2FeS5]2-: Spectroscopic Characterization of Species Relevant to the Nitric Oxide Modification and Repair of [2Fe−2S] Ferredoxins
    Authors: Tsai, Ming-Li;Chen, Chiao-Chun;Hsu, I-Jui;Ke, Shyue-Chu;Hsieh, Chung-Hung;Chiang, Kuo-An;Lee, Gene-Hsiang;Wang, Yu;Chen, Jin-Ming;Lee, Jyh-Fu;Liaw, Wen-Feng
    Contributors: 淡江大學化學學系
    Date: 2004-08
    Issue Date: 2014-03-27 14:57:04 (UTC+8)
    Publisher: Washington, DC: American Chemical Society
    Abstract: The reaction of [PPN][Fe(CO)3(NO)] and S8 in a 1:1 molar ratio in THF proceeded to give the dinitrosyl iron complex [PPN][S5Fe(NO)2] (1) and the known [PPN]2[S5Fe(μ-S)2FeS5] (2). EPR signals of g values gz = 2.0148, gx = 2.0270, and gy = 2.0485 at 77 K confirmed the existence of the unpaired electron in compound 1. The temperature-dependent magnetic moment of complex 1 indicates that the ground state is one unpaired electron with (St, SL) = (1/2, 1) at very low temperature (St is the total spin quantum number of the system; SL is the sum of the spin quantum numbers of two NO ligands). The O K-edge absorptions of complex 1 and [(NO)Fe(S2CNEt2)2] at 532.1 and 532.5 eV are assigned to the transition of 1s → π*(NO) and 1s → π*(NO+), respectively. For the electronic structure of the {Fe(NO)2} core, DFT calculations, magnetic susceptibility measurement, EPR, and Fe K-/L-edge XAS spectroscopy of complex 1 lead to a description of {Fe1+(•NO)2}9. [2Fe−2S] cluster 2 treated with nitric oxide in THF shows that cluster 2 is transformed into the dinitrosyl iron complex 1 identified by IR, UV−vis, and X-ray diffraction analysis. The reaction may be reversed by the photolysis of the THF solution of 1 in the presence of the NO-accepting reagent [(C4H8O)Fe(S,S-C6H4)2]- to reform 2. This result demonstrates a successful biomimetic reaction cycle of the degradation and reassembly of [2Fe−2S] cluster [S5Fe(μ-S)2FeS5]2- relevant to the repair of nitric oxide-modified [2Fe−2S] ferredoxin by cysteine desulfurase and l-cysteine in vitro.
    Relation: Inorganic Chemistry 43(16), pp.5159-5167
    DOI: 10.1021/ic0494915
    Appears in Collections:[Graduate Institute & Department of Chemistry] Journal Article

    Files in This Item:

    File Description SizeFormat

    All items in 機構典藏 are protected by copyright, with all rights reserved.

    DSpace Software Copyright © 2002-2004  MIT &  Hewlett-Packard  /   Enhanced by   NTU Library & TKU Library IR teams. Copyright ©   - Feedback