| Literature DB >> 27387959 |
Leland B Gee1, Chun-Yi Lin1, Francis E Jenney2, Michael W W Adams2, Yoshitaka Yoda3, Ryo Masuda4, Makina Saito4, Yasuhiro Kobayashi4, Kenji Tamasaku5, Michael Lerche1, Makoto Seto4,6, Charles G Riordan7, Ann Ploskonka7, Philip P Power1, Stephen P Cramer1,8, Lars Lauterbach1,9.
Abstract
We used a novel experimental setup to conduct the first synchrotron-based (61)Ni Mössbauer spectroscopy measurements in the energy domain on Ni coordination complexes and metalloproteins. A representative set of samples was chosen to demonstrate the potential of this approach. (61)NiCr2O4 was examined as a case with strong Zeeman splittings. Simulations of the spectra yielded an internal magnetic field of 44.6 T, consistent with previous work by the traditional (61)Ni Mössbauer approach with a radioactive source. A linear Ni amido complex, (61)Ni{N(SiMe3)Dipp}2, where Dipp = C6H3-2,6-(i)Pr2, was chosen as a sample with an "extreme" geometry and large quadrupole splitting. Finally, to demonstrate the feasibility of metalloprotein studies using synchrotron-based (61)Ni Mössbauer spectroscopy, we examined the spectra of (61)Ni-substituted rubredoxin in reduced and oxidized forms, along with [Et4N]2[(61)Ni(SPh)4] as a model compound. For each of the above samples, a reasonable spectrum could be obtained in ∼1 d. Given that there is still room for considerable improvement in experimental sensitivity, synchrotron-based (61)Ni Mössbauer spectroscopy appears to be a promising alternative to measurements with radioactive sources.Entities:
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Year: 2016 PMID: 27387959 PMCID: PMC6813798 DOI: 10.1021/acs.inorgchem.5b03004
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165