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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical chemistry accounts 105 (2000), S. 145-155 
    ISSN: 1432-2234
    Keywords: Key words: Potential-energy surface ; Reaction-path following ; Saddle point ; Reduced gradient ; Gradient extremal
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract. A simple procedure with low computational efforts is proposed to follow the reaction path of the potential-energy hypersurface (PES) starting from minima or saddle points. The method uses a modification of the so-called “following the reduced gradient” [Quapp W, Hirsch M, Imig O, Heidrich D (1998) J Comput Chem 19:1087]. The original method connects points where the gradient has a constant direction. In the present article the procedure is replaced by taking iterative varying directions of the gradient controlled by the last tangent of the searched curve. The resulting minimum energy path is that valley floor gradient extremal (GE) which belongs to the smallest (absolute) eigenvalue of the Hessian and, hence, that GE which usually leads along the streambed of a chemical reaction. The new method avoids third derivatives of the PES and obtains the GE of least ascent by second-order calculations only. Nevertheless, we are able to follow the streambed GE uphill or downhill. We can connect a minimum with its saddles if the streambed leads up to a saddle, or we find a turning point or a bifurcation point. The effectiveness and the characteristic properties of the new algorithm are demonstrated by using polynomial test surfaces, an ab initio PES of H2O, and the analytic potentials of Lennard-Jones (LJ) clusters. By tracing the streambeds we located previously identified saddle points for LJ N with N=3, 7, 8, and 55. Saddles for LJ N with N=15, 20, and 30 as presented here are new results.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Computational Chemistry 19 (1998), S. 1087-1100 
    ISSN: 0192-8651
    Keywords: saddle point ; distinguished coordinate ; valley-ridge inflection point ; H2CO potential energy surface ; HCN⇌CNH isomerization ; azidoazomethine⇌1H-tetrazole isomerization ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Computer Science
    Notes: The old coordinate driving procedure to find transition structures in chemical systems is revisited. The well-known gradient criterion, ∇E(x)=0, which defines the stationary points of the potential energy surface (PES), is reduced by one equation corresponding to one search direction. In this manner, abstract curves can be defined connecting stationary points of the PES. Starting at a given minimum, one follows a well-selected coordinate to reach the saddle of interest. Usually, but not necessarily, this coordinate will be related to the reaction progress. The method, called reduced gradient following (RGF), locally has an explicit analytical definition. We present a predictor-corrector method for tracing such curves. RGF uses the gradient and the Hessian matrix or updates of the latter at every curve point. For the purpose of testing a whole surface, the six-dimensional PES of formaldehyde, H2CO, was explored by RGF using the restricted Hartree-Fock (RHF) method and the STO-3G basis set. Forty-nine minima and saddle points of different indices were found. At least seven stationary points representing bonded structures were detected in addition to those located using another search algorithm on the same level of theory. Further examples are the localization of the saddle for the HCN⇌CNH isomerization (used for steplength tests) and for the ring closure of azidoazomethine to 1H-tetrazole. The results show that following the reduced gradient may represent a serious alternative to other methods used to locate saddle points in quantum chemistry.   © 1998 John Wiley & Sons, Inc.   J Comput Chem 19: 1087-1100, 1998
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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