Density functional theory study of the oxidation of methanol to formaldehyde on a hydrated vanadia cluster

Journal of Computational Chemistry
P González-NavarreteJ Andrés

Abstract

Density functional theory was used to study the mechanism for the oxidation of methanol to formaldehyde. A vanadium oxide cluster O=V(OH)(3) has been utilized to represent the catalytic system under hydrated conditions, i.e., in the presence of V-OH hydroxyl groups. Two types of methoxy-intermediates have been considered: a penta-coordinate methoxy-intermediate (OH)(4)V(OCH(3)) and a tetrahedral methoxy-intermediate (OH)(2)VO(OCH(3))(H(2)O). The most plausible reaction pathway corresponds to the process involving first the formation of the tetrahedral methoxide, and a subsequent rate-limiting step where hydrogen is transferred from the methoxy groups toward the oxygen atom of the vanadyl V=O site. The reaction mechanism is a typical two-state reactivity process due to a change of the multiplicity (reactive singlet --> product triplet) along the reaction coordinate accompanied by a reduction of the vanadium center from V(V) (d(0)) to V(III) (d(2)). Minimum energy crossing points were localized and possible spin inversion processes are discussed by means of the intrinsic reaction coordinate approach to find the most favorable reaction pathways. The hydration effect is found to be mainly the destabilization of the methoxy intermed...Continue Reading

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Citations

Dec 30, 2017·The Journal of Physical Chemistry. a·Patricio González-NavarreteMonica Calatayud

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