TY - JOUR

T1 - Reaction-path potential and vibrational frequencies in terms of curvilinear internal coordinates

AU - Jackels, Charles F.

AU - Gu, Zhen

AU - Truhlar, Donald G.

PY - 1995

Y1 - 1995

N2 - We present a general formulation that allows physically intuitive curvilinear internal coordinates to be used for the calculation of potential energy expansions and generalized normal-mode vibrational frequencies in reaction-path calculations. The reaction path is defined, as usual, as the minimum-energy path in the mass-scaled Cartesian coordinate system, and curvilinear coordinates are used for vibrational frequency calculations at nonstationary points. The method is well adapted for use in variational transition state theory with semiclassical multidimensional tunneling (VTST/ MT) approximations to calculate thermal rate constants. We present VTST/MT calculations for five reactions, H+H2→H2+H, O+H 2→OH+H, CH3+H2→CH4+H, H+O2→HO2, and Cl+HBr→HCl+Br, to illustrate the use of the new curvilinear coordinates, and we compare the results to calculations employing rectilinear coordinates. We make detailed comparisons not only of the calculated rate constants but also of the vibrationally adiabatic ground-state potential energy curves and bound-state vibrational frequencies as functions of the reaction coordinate.

AB - We present a general formulation that allows physically intuitive curvilinear internal coordinates to be used for the calculation of potential energy expansions and generalized normal-mode vibrational frequencies in reaction-path calculations. The reaction path is defined, as usual, as the minimum-energy path in the mass-scaled Cartesian coordinate system, and curvilinear coordinates are used for vibrational frequency calculations at nonstationary points. The method is well adapted for use in variational transition state theory with semiclassical multidimensional tunneling (VTST/ MT) approximations to calculate thermal rate constants. We present VTST/MT calculations for five reactions, H+H2→H2+H, O+H 2→OH+H, CH3+H2→CH4+H, H+O2→HO2, and Cl+HBr→HCl+Br, to illustrate the use of the new curvilinear coordinates, and we compare the results to calculations employing rectilinear coordinates. We make detailed comparisons not only of the calculated rate constants but also of the vibrationally adiabatic ground-state potential energy curves and bound-state vibrational frequencies as functions of the reaction coordinate.

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U2 - 10.1063/1.468630

DO - 10.1063/1.468630

M3 - Article

AN - SCOPUS:36449008542

SN - 0021-9606

VL - 102

SP - 3188

EP - 3201

JO - The Journal of chemical physics

JF - The Journal of chemical physics

IS - 8

ER -