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• W1994364824 endingPage "2585" @default.
• W1994364824 startingPage "2579" @default.
• W1994364824 abstract "Theoretical studies of the stereodynamics for the chemical reaction H + LiH+(v = 0, j = 0) → Li++ H2 were conducted using the quasi-classical trajectory (QCT) method on the three-dimensional potential energy surface [J. Chem. Phys. 119, 11241 (2003)] at three collision energies (0.01, 0.05 and 0.1 eV). The calculated DCS results indicate that the products tend to both extreme forward and backward scattering. Because the potential well lying in the product valley is a weak van der Waals well, the forward–backward scattering is asymmetric. The calculated P(θr ) shows that the rotational angular momentum polarization of the product molecule is quite strong and insensitive to increasing collision energy. For the title reaction, it is not a deep well but a shallow Van der Waals well about 0.286 eV below the Li++ H2 asymptote on the PES. Hence, the reaction mainly behaves as an exoergic reaction rather than an insertion mechanism. The distributions of indicate that j′ is not only aligned, but also oriented preferentially along the positive direction of the y-axis. The distributions indicate that the product molecules are preferentially polarized perpendicular to the scattering plane and that the reaction is dominated by an in-plane mechanism." @default.
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• W1994364824 date "2009-12-10" @default.
• W1994364824 modified "2023-10-18" @default.
• W1994364824 title "Theoretical studies of the stereodynamics for the reaction H + LiH⁺(<i>v</i>= 0,<i>j</i>= 0) → Li⁺+ H₂" @default.
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• W1994364824 doi "https://doi.org/10.1080/00268970903430966" @default.
• W1994364824 hasPublicationYear "2009" @default.
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