X-ray Absorption Spectroscopy of a Structural Analogue of the Oxidized Active Sites in the Sulfite Oxidase Enzyme Family and Related Molybdenum(V) Complexes

2003 ◽  
Vol 42 (18) ◽  
pp. 5531-5536 ◽  
Author(s):  
Farideh Jalilehvand ◽  
Booyong S. Lim ◽  
R. H. Holm ◽  
Britt Hedman ◽  
Keith O. Hodgson



1997 ◽  
Vol 67 (1-4) ◽  
pp. 424
Author(s):  
Keith O. Hodgson ◽  
Britt Hedman ◽  
Hua Holly Zhang


2000 ◽  
Vol 2 (15) ◽  
pp. 3473-3481 ◽  
Author(s):  
Th. Schedel-Niedrig ◽  
M. Hävecker ◽  
A. Knop-Gericke ◽  
R. Schlögl


2001 ◽  
Vol 123 (34) ◽  
pp. 8343-8349 ◽  
Author(s):  
Booyong S. Lim ◽  
Michael W. Willer ◽  
Mingming Miao ◽  
R. H. Holm


Author(s):  
Yang Liu ◽  
Avik Halder ◽  
Soenke Seifert ◽  
Nicholas Marcella ◽  
Stefan Vajda ◽  
...  


1999 ◽  
Vol 38 (10) ◽  
pp. 2539-2540 ◽  
Author(s):  
Graham N. George ◽  
Ingrid J. Pickering ◽  
Caroline Kisker




1979 ◽  
Vol 101 (10) ◽  
pp. 2772-2774 ◽  
Author(s):  
Stephen P. Cramer ◽  
Harry B. Gray ◽  
K. V. Rajagopalan


Biochemistry ◽  
1989 ◽  
Vol 28 (12) ◽  
pp. 5075-5080 ◽  
Author(s):  
Graham N. George ◽  
Cary A. Kipke ◽  
Roger C. Prince ◽  
Roger A. Sunde ◽  
John H. Enemark ◽  
...  


2021 ◽  
Author(s):  
Justin T. Henthorn ◽  
Serena DeBeer

Selenium X-ray absorption spectroscopy (XAS) has found widespread use in investigations of Se-containing materials, geochemical processes, and biological active sites. In contrast to sulfur Kβ X-ray emission spectroscopy (XES), which has been found to contain electronic and structural information complementary to S XAS, Se Kβ XES remains comparatively under-explored. Herein, we present the first Se Valence-to-Core (VtC) XES studies of reduced Se-containing compounds and FeSe dimers. Se VtC XES is found to be sensitive to changes in covalent Se bonding interactions (Se–Se/Se–C/Se–H bonding) while relatively insensitive to changes in Fe oxidation states as selenide bridges in FeSe dimers ([Fe2Se2]2+ vs [Fe2Se2]+). Contrastingly, Se Kβ HERFD XAS is demonstrated to be quite sensitive to changes in Fe-oxidation state, with Se Kβ HERFD XAS demonstrating experimental resolution equivalent to K𝛼 HERFD XAS. Additionally, computational studies reveal both Se VtC XES and XAS to be sensitive to selenium protonation in FeSe complexes.



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