| Literature DB >> 29696767 |
Sreekanta Debnath1,2, Harald Knorke1, Wieland Schöllkopf2, Shaodong Zhou3,4, Knut R Asmis1, Helmut Schwarz3.
Abstract
Cryogenic ion vibrational spectroscopy was used in combination with electronic structure calculations to identify the active site in the oxygen atom transfer reaction [AlVO4 ]+. +CO→[AlVO3 ]+. +CO2 . Infrared photodissociation spectra of messenger-tagged heteronuclear clusters demonstrate that in contrast to [AlVO4 ]+. , [AlVO3 ]+. is devoid of a terminal Al-Ot unit while the terminal V=Ot group remains intact. Thus it is the Al-Ot moiety that forms the active site in the [AlVOx ]+. /CO/N2 O (x=3, 4) redox couples, which is in line with theoretical predictions.Entities:
Keywords: active-site characterization; heteronuclear cluster oxides; infrared photodissociation spectroscopy; redox catalysis
Year: 2018 PMID: 29696767 DOI: 10.1002/anie.201804056
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336