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X-ray absorption spectroscopic studies of mononuclear non-heme iron enzymes
Author(s) -
Tami E. Westre
Publication year - 1996
Language(s) - English
Resource type - Reports
DOI - 10.2172/531115
Subject(s) - extended x ray absorption fine structure , x ray absorption spectroscopy , oxidation state , chemistry , heme , absorption (acoustics) , absorption spectroscopy , xanes , coordination sphere , crystallography , analytical chemistry (journal) , spectroscopy , materials science , enzyme , metal , physics , optics , biochemistry , organic chemistry , crystal structure , composite material , quantum mechanics
Fe-K-edge X-ray absorption spectroscopy (XAS) has been used to investigate the electronic and geometric structure of the iron active site in non-heme iron enzymes. A new theoretical extended X-ray absorption fine structure (EXAFS) analysis approach, called GNXAS, has been tested on data for iron model complexes to evaluate the utility and reliability of this new technique, especially with respect to the effects of multiple-scattering. In addition, a detailed analysis of the 1s{yields}3d pre-edge feature has been developed as a tool for investigating the oxidation state, spin state, and geometry of iron sites. Edge and EXAFS analyses have then been applied to the study of non-heme iron enzyme active sites.

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