A quasiclassical trajectory study of the state specific H+D-2(v=0, j=0)-> HD(v'=0, j'=0)+D reaction at a collision energy of 1.85 eV (total energy of 2.04 eV) found that the scattering is governed by two unexpected and dominant new mechanisms, and not by direct recoil as is generally assumed. The new mechanisms involve strong interaction with the sloping potential around the conical intersection, an area of the potential energy surface not previously considered to have much effect upon reactive scattering. Initial investigations indicate that more than 50% of reactive scattering could be the result of these new mechanisms at this collision energy. Features in the corresponding quantum mechanical results can be attributed to these new (class...
The collinear hydrogen exchange reaction is a paradigm system for understanding chemical reactions. ...
We report rovibrationally selected differential cross sections (DCSs) of the benchmark reaction H + ...
Reaction resonance is a frontier topic in chemical dynamics research, and it is aiso essential to th...
The time-delayed forwards scattering mechanism recently observed by Althorpe et al. [1] for the H + ...
Accurate three‐dimensional reactive and nonreactive quantum mechanical cross sections for the H+H_2 ...
10 págs.; 10 figs.; 1 tab.; Special Issue: Dynamics of Molecular Collisions XXV: Fifty Years of Chem...
The results of an accurate quantum mechanical treatment of the planar H+H_2 exchange reaction on a r...
Journal ArticleA quasi-classical study of the endoergic Au+(¹S) + H₂(X¹Σ+g) → AuH+ (²Σ+) + H(²S) rea...
The title reaction has been studied both experimentally and computationally at a mean collision ener...
The absolute value of the cross section for the abstraction reaction between fast H atoms and H2O ha...
This review focuses on experimental studies of the dynamical outcomes following collisional quenchin...
The following article appeared in Journal of Chemical Physic 135.9 (2011): 091102 and may be found a...
Time-independent quantum mechanical (TIQM) approach (helicity basis truncated at k=2) has been used ...
Time-dependent quantum mechanical wave packet calculations have been carried out to study ...
12 págs.; 12 figs.; 1 tab.; Special Issue: Dynamics of Molecular Collisions XXV: Fifty Years of Chem...
The collinear hydrogen exchange reaction is a paradigm system for understanding chemical reactions. ...
We report rovibrationally selected differential cross sections (DCSs) of the benchmark reaction H + ...
Reaction resonance is a frontier topic in chemical dynamics research, and it is aiso essential to th...
The time-delayed forwards scattering mechanism recently observed by Althorpe et al. [1] for the H + ...
Accurate three‐dimensional reactive and nonreactive quantum mechanical cross sections for the H+H_2 ...
10 págs.; 10 figs.; 1 tab.; Special Issue: Dynamics of Molecular Collisions XXV: Fifty Years of Chem...
The results of an accurate quantum mechanical treatment of the planar H+H_2 exchange reaction on a r...
Journal ArticleA quasi-classical study of the endoergic Au+(¹S) + H₂(X¹Σ+g) → AuH+ (²Σ+) + H(²S) rea...
The title reaction has been studied both experimentally and computationally at a mean collision ener...
The absolute value of the cross section for the abstraction reaction between fast H atoms and H2O ha...
This review focuses on experimental studies of the dynamical outcomes following collisional quenchin...
The following article appeared in Journal of Chemical Physic 135.9 (2011): 091102 and may be found a...
Time-independent quantum mechanical (TIQM) approach (helicity basis truncated at k=2) has been used ...
Time-dependent quantum mechanical wave packet calculations have been carried out to study ...
12 págs.; 12 figs.; 1 tab.; Special Issue: Dynamics of Molecular Collisions XXV: Fifty Years of Chem...
The collinear hydrogen exchange reaction is a paradigm system for understanding chemical reactions. ...
We report rovibrationally selected differential cross sections (DCSs) of the benchmark reaction H + ...
Reaction resonance is a frontier topic in chemical dynamics research, and it is aiso essential to th...