In Part I, activated‐complex theory was extended by including the possibility of a curvilinear reaction coordinate. A separation‐of‐variables approximation was made in the neighborhood of the activated‐complex region of configuration space. In the present paper a more general yet simpler derivation of the final equation is given. It permits subsequent introduction of analytical mechanics in the above neighborhood in a variety of ways such as separation of variables, vibrational adiabaticity, or a method combining certain features of both, the separable—adiabatic approximation. The relationship of these methods is discussed. Some numerical quantum‐ and classical‐mechanical results obtained for transmission coefficients of nonrotating atom‐t...
The equations of Part I for the specific and over‐all unimolecular reaction‐rate constants are exten...
Separation of the Schrödinger equation for molecular dynamics into sets of variables can sometimes b...
Conversion of translational into vibrational energy during the last step of a unimolecular reaction ...
Co-ordinates and "vibrationally-adiabatic" approximations are described for reactions in three dimen...
Co-ordinates and "vibrationally-adiabatic" approximations are described for reactions in three dimen...
The analytical quantum mechanics of chemically reactive linear collisions is treated in the vibratio...
In its usual classical form, activated‐complex theory assumes a particular expression for the kineti...
The analytical quantum mechanics of chemically reactive linear collisions is treated in the vibratio...
The natural collision coordinates of Part III are used to treat the analytical mechanics of chemical...
The classical mechanics of chemically reactive linear collisions is investigated for vibrationally n...
In its usual form activated complex theory assumes a quasi-equilibrium between reactants and activat...
Natural collision coordinates and a zeroth‐order vibrational–adiabatic approximation are used to tre...
Rotational and vibrational distributions for the exchange reaction H+H_(2)→H_(2)+H are obtained nume...
The classical mechanics of chemically reactive linear collisions is investigated for vibrationally n...
The activated-complex theory of chemical reactions has proved to be very useful in interpreting rat...
The equations of Part I for the specific and over‐all unimolecular reaction‐rate constants are exten...
Separation of the Schrödinger equation for molecular dynamics into sets of variables can sometimes b...
Conversion of translational into vibrational energy during the last step of a unimolecular reaction ...
Co-ordinates and "vibrationally-adiabatic" approximations are described for reactions in three dimen...
Co-ordinates and "vibrationally-adiabatic" approximations are described for reactions in three dimen...
The analytical quantum mechanics of chemically reactive linear collisions is treated in the vibratio...
In its usual classical form, activated‐complex theory assumes a particular expression for the kineti...
The analytical quantum mechanics of chemically reactive linear collisions is treated in the vibratio...
The natural collision coordinates of Part III are used to treat the analytical mechanics of chemical...
The classical mechanics of chemically reactive linear collisions is investigated for vibrationally n...
In its usual form activated complex theory assumes a quasi-equilibrium between reactants and activat...
Natural collision coordinates and a zeroth‐order vibrational–adiabatic approximation are used to tre...
Rotational and vibrational distributions for the exchange reaction H+H_(2)→H_(2)+H are obtained nume...
The classical mechanics of chemically reactive linear collisions is investigated for vibrationally n...
The activated-complex theory of chemical reactions has proved to be very useful in interpreting rat...
The equations of Part I for the specific and over‐all unimolecular reaction‐rate constants are exten...
Separation of the Schrödinger equation for molecular dynamics into sets of variables can sometimes b...
Conversion of translational into vibrational energy during the last step of a unimolecular reaction ...