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    Synthesis and characterization of an iron complex bearing a cyclic tetra-N-heterocyclic carbene ligand: An artifical heme analogue?

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    Type
    Article
    Authors
    Anneser, Markus R.
    Haslinger, Stefan
    Pöthig, Alexander
    Cokoja, Mirza
    Basset, Jean-Marie cc
    Kühn, Fritz
    KAUST Department
    Chemical Science Program
    KAUST Catalysis Center (KCC)
    Physical Science and Engineering (PSE) Division
    Date
    2015-04-06
    Online Publication Date
    2015-04-06
    Print Publication Date
    2015-04-20
    Permanent link to this record
    http://hdl.handle.net/10754/564145
    
    Metadata
    Show full item record
    Abstract
    An iron(II) complex with a cyclic tetradentate ligand containing four N-heterocyclic carbenes was synthesized and characterized by means of NMR and IR spectroscopies, as well as by single-crystal X-ray structure analysis. The iron center exhibits an octahedral coordination geometry with two acetonitrile ligands in axial positions, showing structural analogies with porphyrine-ligated iron complexes. The acetonitrile ligands can readily be substituted by other ligands, for instance, dimethyl sulfoxide, carbon monoxide, and nitric oxide. Cyclic voltammetry was used to examine the electronic properties of the synthesized compounds. © 2015 American Chemical Society.
    Citation
    Anneser, M. R., Haslinger, S., Pöthig, A., Cokoja, M., Basset, J.-M., & Kühn, F. E. (2015). Synthesis and Characterization of an Iron Complex Bearing a Cyclic Tetra-N-heterocyclic Carbene Ligand: An Artifical Heme Analogue? Inorganic Chemistry, 54(8), 3797–3804. doi:10.1021/ic503043h
    Sponsors
    M.R.A. and S.H. gratefully acknowledge support by the TUM Graduate School. This project was supported through a collaboration with the King Abdullah University of Saudi-Arabia (Grant No. KSA-00069/UKC0020).
    Publisher
    American Chemical Society (ACS)
    Journal
    Inorganic Chemistry
    DOI
    10.1021/ic503043h
    PubMed ID
    25843109
    Relations
    Is Supplemented By:
    • [Dataset]
      Anneser, M. R., Haslinger, S., Pöthig, A., Cokoja, M., Basset, J.-M., & Kühn, F. E. (2015). CCDC 963848: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc11byw6. DOI: 10.5517/cc11byw6 HANDLE: 10754/624263
    • [Dataset]
      Anneser, M. R., Haslinger, S., Pöthig, A., Cokoja, M., Basset, J.-M., & Kühn, F. E. (2015). CCDC 1036601: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc13snr9. DOI: 10.5517/cc13snr9 HANDLE: 10754/624390
    • [Dataset]
      Anneser, M. R., Haslinger, S., Pöthig, A., Cokoja, M., Basset, J.-M., & Kühn, F. E. (2015). CCDC 1036602: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc13snsb. DOI: 10.5517/cc13snsb HANDLE: 10754/624391
    • [Dataset]
      Anneser, M. R., Haslinger, S., Pöthig, A., Cokoja, M., Basset, J.-M., & Kühn, F. E. (2015). CCDC 1036603: Experimental Crystal Structure Determination [Data set]. Cambridge Crystallographic Data Centre. https://doi.org/10.5517/cc13sntc. DOI: 10.5517/cc13sntc HANDLE: 10754/624392
    ae974a485f413a2113503eed53cd6c53
    10.1021/ic503043h
    Scopus Count
    Collections
    Articles; Physical Science and Engineering (PSE) Division; Chemical Science Program; KAUST Catalysis Center (KCC)

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