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  • 1
    ISSN: 0948-5023
    Keywords: Gas phase ion pairs ; Multiple proton exchange ; Ab initio calculations ; Density functional calculations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract High level ab initio and density functional calculations, extrapolated to QCISD(T)/6-311+G(3df,2p)//MP2/6-31+G**+ZPE, reveal that cyclic ion pairs can form in the hydrogen bonded complexes of haloboric acids BHnX3-n–HX, X=F, Cl, with Lewis bases HX, H2O, CH3OH, and NH3, even in isolation (e.g., in the gas phase). The intrinsic acidities (deprotonation energies) required for protonation of these bases with formation of gas phase ion pairs are calculated to be 〈295 kcal/mol for water, 〈301 kcal/mol for methanol, and 〈306 kcal/mol for ammonia; such values are common for acidic sites in zeolites. All gas phase ion pairs prefer symmetric bidentate or tridentate structures. In the other cases where hydrogen bonded complexes prevail, symmetric ion pair-like transition structures for multiple hydrogen exchange are computed.
    Type of Medium: Electronic Resource
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  • 2
    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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