| Literature DB >> 29847703 |
Vladimir Pelmenschikov1, Leland B Gee2,3, Hongxin Wang2, K Cory MacLeod4, Sean F McWilliams4, Kazimer L Skubi4, Stephen P Cramer2, Patrick L Holland4.
Abstract
High-spin iron species with bridging hydrides have been detected in species trapped during nitrogenase catalysis, but there are few general methods of evaluating Fe-H bonds in high-spin multinuclear iron systems. An 57 Fe nuclear resonance vibrational spectroscopy (NRVS) study on an Fe(μ-H)2 Fe model complex reveals Fe-H stretching vibrations for bridging hydrides at frequencies greater than 1200 cm-1 . These isotope-sensitive vibrational bands are not evident in infrared (IR) spectra, showing the power of NRVS for identifying hydrides in this high-spin iron system. Complementary density functional theory (DFT) calculations elucidate the normal modes of the rhomboidal iron hydride core.Entities:
Keywords: density functional theory; iron hydrides; nitrogenases; nuclear resonance vibrational spectroscopy
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Year: 2018 PMID: 29847703 PMCID: PMC6098820 DOI: 10.1002/anie.201804601
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336