Examination of the Mechanism of the Yield of N2O from Nitroxyl (HNO) in the Solution Phase by Theoretical Calculations

Kaiqiang Zhang, Stefan T. Thynell

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4 Scopus citations

Abstract

The dimerization of HNO and subsequent yield of N2O in aqueous solution are studied based on the theoretical calculations and kinetic simulations. The initial dimerization reactions were computed at various levels of theory, and large divergence was observed in the predictions of the gas-phase free energies. The T1 diagnostics at CCSD(T)/aug-cc-pVTZ suggests multireference characteristics of the HNO dimers and the transition states. The solution-phase free energies were obtained using the wB97XD method and the SMD solvation model. The pKa values of the (HNO)2 tautomers and their first protonated and deprotonated products were estimated using the cluster-continuum approach. The theoretical results confirmed the original conclusion that the favored cis-pathway is comprised of several rapid proton transfer steps leading to either cis-HONNOH or cis-HONNŌ before decomposition. Several new water-catalyzed and H3O+/water catalyzed reactions are presented to explain the fast kinetics observed in the experiments. To validate the proposed mechanism, kinetic simulations with the consideration of diffusion-limited kinetics were implemented on several related systems, based on which the previously reported global rate constant was explained as the kinetics of the initial dimerization step and the global kinetics in very dilute HNO solutions.

Original languageEnglish (US)
Pages (from-to)4505-4516
Number of pages12
JournalJournal of Physical Chemistry A
Volume121
Issue number23
DOIs
StatePublished - Jun 15 2017

All Science Journal Classification (ASJC) codes

  • Physical and Theoretical Chemistry

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