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• W2947767303 startingPage "5347" @default.
• W2947767303 abstract "The dynamics of the N2 + HOC+ multichannel reaction is investigated up to 1.0 eV of collision energy on an accurate global potential energy surface (PES) for the ground electronic state. The PES is constructed using the permutation invariant polynomial-neural network (PIP-NN) method by fitting ∼37 000 points at the CCSD(T)-F12a/cc-pVTZ-F12 level with a root-mean-square error of about 3.0 meV. It was found that the total reaction integral cross section decreases monotonically with the collision energy, consistent with the barrierless complex-forming mechanism. Throughout the energy range, the proton transfer channel, which leads to the N2H+ + CO products, dominates the proton isomerization channel, which forms the N2 + HCO+ products. The differential cross section of the proton transfer channel is backward biased, signaling a relatively direct process, while that of the proton isomerization channel shows strong forward-backward symmetry, which can be attributed to a long-lived intermediate." @default.
• W2947767303 created "2019-06-07" @default.
• W2947767303 creator A5023516505 @default.
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• W2947767303 date "2019-05-30" @default.
• W2947767303 modified "2023-10-06" @default.
• W2947767303 title "Competition between Proton Transfer and Proton Isomerization in the N₂ + HOC⁺ Reaction on an <i>Ab Initio</i>-Based Global Potential Energy Surface" @default.
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• W2947767303 doi "https://doi.org/10.1021/acs.jpca.9b04115" @default.
• W2947767303 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/31146531" @default.
• W2947767303 hasPublicationYear "2019" @default.
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