Characterization of homologous divalent metal ion binding sites of vertebrate and molluscan myosins using electron paramagnetic resonance spectroscopy

1979 ◽  
Vol 130 (3) ◽  
pp. 317-336 ◽  
Author(s):  
Clive R. Bagshaw ◽  
John Kendrick-Jones
Keyword(s):  
Metal Ion ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Metal Ion Binding ◽  
Paramagnetic Resonance ◽  
Divalent Metal Ion ◽  
Ion Binding Sites ◽  
Metal Ion Binding Sites ◽  
Electron Paramagnetic

scholarly journals Characterization of neutrophilb-type cytochrome in situ by electron paramagnetic resonance spectroscopy

FEBS Letters ◽  
1991 ◽  
Vol 281 (1-2) ◽  
pp. 130-132 ◽  
Author(s):  
Ikuko Ueno ◽  
Satoshi Fujii ◽  
Hiroaki Ohya-Nishiguchi ◽  
Tetsutaro Iizuka ◽  
Shiro Kanegasaki
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Paramagnetic Resonance ◽  
Electron Paramagnetic

Characterization of titanium dopants in sodium alanate by electron paramagnetic resonance spectroscopy

2005 ◽  
Vol 20 (12) ◽  
pp. 3265-3269 ◽  
Author(s):  
Meredith T. Kuba ◽  
Sandra S. Eaton ◽  
Christine Morales ◽  
Craig M. Jensen
Keyword(s):  
Electron Paramagnetic Resonance ◽  
Electron Paramagnetic Resonance Spectroscopy ◽  
Epr Spectra ◽  
Minor Amount ◽  
Resonance Spectroscopy ◽  
Paramagnetic Resonance ◽  
Dehydrogenation Kinetics ◽  
Electron Paramagnetic ◽  
Kinetics Of

Electron paramagnetic resonance (EPR) spectra were obtained for samples of Ti-doped NaAlH4 subjected to different numbers of cycles of dehydrogenation/re-hydrogenation. Ti is observed to evolve from its initial Ti(III) state through a series of Ti(0) species during the first 5 cycles. Although the conversion of Ti(III) to Ti(0) occurs much more readily for TiCl3-doped samples than those prepared with TiF3, in both cases the evolution of Ti follows the same sequence that involves 3 distinguishable Ti(0) species and ends in the predominance of the same single Ti(0) species. The spectrum of a sample of NaAlH4 containing 2 mol% of cubic Al3Ti is distinctly different than any of those observed for the Ti(0) species that arise during the hydrogen cycling of the hydride. The major changes in the nature of the predominant Ti species have little if any effect on the dehydrogenation kinetics, which strongly suggests that the profoundly enhanced hydrogen cycling kinetics of Ti-doped NaAlH4 are due to a Ti species present in only a relatively minor amount.

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