Following a Chemical Reaction on the Millisecond Time Scale by Simultaneous X-ray and UV/Vis Spectroscopy
Overview
Authors
Affiliations
An innovative approach aimed at disclosing the mechanism of chemical reactions occurring in solution on the millisecond time scale is presented. Time-resolved energy dispersive X-ray absorption and UV/vis spectroscopies with millisecond resolution are used simultaneously to directly follow the evolution of both the oxidation state and the local structure of the metal center in an iron complex. Two redox reactions are studied, the former involving the transformation of Fe into two subsequent Fe species and the latter involving the more complex Fe-Fe-Fe-Fe sequence. The structural modifications occurring around the iron center are correlated to the reaction mechanisms. This combined approach has the potential to provide unique insights into reaction mechanisms in the liquid phase and represents a new powerful tool to characterize short-lived intermediates that are silent to common spectroscopic techniques.
Zero- to low-field relaxometry of chemical and biological fluids.
Alcicek S, Put P, Kubrak A, Alcicek F, Barskiy D, Gloeggler S Commun Chem. 2023; 6(1):165.
PMID: 37542142 PMC: 10403525. DOI: 10.1038/s42004-023-00965-8.
Kimura Y, Inagawa A, Uehara N Anal Sci. 2023; 39(8):1425-1432.
PMID: 37097514 DOI: 10.1007/s44211-023-00348-y.
Direct Mechanistic Evidence for a Nonheme Complex Reaction through a Multivariate XAS Analysis.
Tavani F, Martini A, Capocasa G, Di Stefano S, Lanzalunga O, DAngelo P Inorg Chem. 2020; 59(14):9979-9989.
PMID: 32598841 PMC: 8008396. DOI: 10.1021/acs.inorgchem.0c01132.