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- W2018334792 abstract "Abstract A possibility of multiplicity change for ground‐state molecular oxygen adsorbed on the surface of regular and doped broad‐gap ionic crystals was considered in the framework of cluster approximation by using SCF MO LCAO quantum chemical methods [semiempirical INDO approximation and ab initio calculation with the 6‐311G** basis set taking into account the correlation effects on the level of second‐order Meller–Plesset perturbation theory (MP2)]. The formation energetics of cyclic products of addition reactions of dioxygen in different multiplet states to furan and cis ‐butadiene in the gas phase and on the surface of ionic crystals was considered. (These reactions are typical for the O 2 singlet state in the gas phase.) It is shown that the presence of sites with high effective charge on the crystal surface can result in a situation not requiring, as in the gas phase, multiplicity change in the transition of a system from an initial to the final state, which can significantly affect the kinetic parameters of the reactions. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002" @default.
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- W2018334792 date "2002-04-26" @default.
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- W2018334792 title "Reactivity of molecular oxygen on the surface of ionic crystals" @default.
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- W2018334792 doi "https://doi.org/10.1002/qua.10196" @default.
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