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    Comparison between the Geometric and Electronic Structures and Reactivities of {FeNO}7 and {FeO2}8 Complexes: A Density Functional Theory Study


    Schenk, Gerhard and Pau, Monita Y. M. and Solomon, Edward I. (2004) Comparison between the Geometric and Electronic Structures and Reactivities of {FeNO}7 and {FeO2}8 Complexes: A Density Functional Theory Study. Journal of the American Chemical Society, 126 (2). pp. 505-515. ISSN 0002-7863

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    Abstract

    In a previous study, we analyzed the electronic structure of S ) 3/2 {FeNO}7 model complexes [Brown et al. J. Am. Chem. Soc. 1995, 117, 715-732]. The combined spectroscopic data and SCF-XRSW electronic structure calculations are best described in terms of FeIII (S ) 5/2) antiferromagnetically coupled to NO- (S ) 1). Many nitrosyl derivatives of non-heme iron enzymes have spectroscopic properties similar to those of these model complexes. These NO derivatives can serve as stable analogues of highly labile oxygen intermediates. It is thus essential to establish a reliable density functional theory (DFT) methodology for the geometry and energetics of {FeNO}7 complexes, based on detailed experimental data. This methodology can then be extended to the study of {FeO2}8 complexes, followed by investigations into the reaction mechanisms of non-heme iron enzymes. Here, we have used the model complex Fe- (Me3TACN)(NO)(N3)2 as an experimental marker and determined that a pure density functional BP86 with 10% hybrid character and a mixed triple-ú/double-ú basis set lead to agreement between experimental and computational data. This methodology is then applied to optimize the hypothetical Fe(Me3TACN)(O2)- (N3)2 complex, where the NO moiety is replaced by O2. The main geometric differences are an elongated Fe-O2 bond and a steeper Fe-O-O angle in the {FeO2}8 complex. The electronic structure of {FeO2}8 corresponds to FeIII (S ) 5/2) antiferromagnetically coupled to O2 - (S ) 1/2), and, consistent with the extended bond length, the {FeO2}8 unit has only one FeIII-O2 - bonding interaction, while the {FeNO}7 unit has both ó and ð type FeIII-NO- bonds. This is in agreement with experiment as NO forms a more stable FeIIINO- adduct relative to O2 -. Although NO is, in fact, harder to reduce, the resultant NO- species forms a more stable bond to FeIII relative to O2 - due to the different bonding interactions.

    Item Type: Article
    Additional Information: The definitive version of this article was published in the Journal of the American Chemical Society, 2004, 126 (2), pp 505–515, DOI: 10.1021/ja036715u . Copyright © 2004 American Chemical Society
    Keywords: Geometric; Electronic Structures; Reactivities; {FeNO}7 {FeO2}8 Complexes; non-heme iron enzymes;
    Academic Unit: Faculty of Science and Engineering > Chemistry
    Item ID: 3698
    Depositing User: Gary Schenk
    Date Deposited: 29 May 2012 15:32
    Journal or Publication Title: Journal of the American Chemical Society
    Publisher: American Chemical Society
    Refereed: Yes
    URI:

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