Experimental and computational X-ray emission spectroscopy as a direct probe of protonation states in oxo-bridged Mn(IV) dimers relevant to redox-active metalloproteins.
Inorg Chem
; 52(22): 12915-22, 2013 Nov 18.
Article
em En
| MEDLINE
| ID: mdl-24161081
ABSTRACT
The protonation state of oxo bridges in nature is of profound importance for a variety of enzymes, including the Mn4CaO5 cluster of photosystem II and the Mn2O2 cluster in Mn catalase. A set of dinuclear bis-µ-oxo-bridged Mn(IV) complexes in different protonation states was studied by Kß emission spectroscopy to form the foundation for unraveling the protonation states in the native complex. The valence-to-core regions (valence-to-core XES) of the spectra show significant changes in intensity and peak position upon protonation. DFT calculations were performed to simulate the valence-to-core XES spectra and to assign the spectral features to specific transitions. The Kß(2,5) peaks arise primarily from the ligand 2p to Mn 1s transitions, with a characteristic low energy shoulder appearing upon oxo-bridge protonation. The satellite Kß" peak provides a more direct signature of the protonation state change, since the transitions originating from the 2s orbitals of protonated and unprotonated µ-oxo bridges dominate this spectral region. The energies of the Kß" features differ by ~3 eV and thus are well resolved in the experimental spectra. Additionally, our work explores the chemical resolution limits of the method, namely, whether a mixed (µ-O)(µ-OH2) motif can be distinguished from a symmetric (µ-OH)2 one. The results reported here highlight the sensitivity of Kß valence-to-core XES to single protonation state changes of bridging ligands, and form the basis for further studies of oxo-bridged polymetallic complexes and metalloenzyme active sites. In a complementary paper, the results from X-ray absorption spectroscopy of the same Mn(IV) dimer series are discussed.
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Base de dados:
MEDLINE
Assunto principal:
Oxigênio
/
Complexos de Coordenação
/
Manganês
/
Metaloproteínas
Tipo de estudo:
Prognostic_studies
Idioma:
En
Revista:
Inorg Chem
Ano de publicação:
2013
Tipo de documento:
Article
País de afiliação:
Estados Unidos