Potential energy, calculation

Truhlar D G and Horowitz C J 1978 Functional representation of Liu and Siegbahn s accurate ab initio potential energy calculations for H + H2 J. Chem. Phys. 68 2466... [Pg.2331]

From the potential energy, calculate the Boltzmann factor, exp(—iC(r )/cBT). [Pg.429]

Equations (2) and (3) relate intermolecular interactions to measurable solution thermodynamic properties. Several features of these two relations are worth noting. The first is the test-particle method, an implementation of the potential distribution theorem now widely used in molecular simulations (Frenkel and Smit, 1996). In the test-particle method, the excess chemical potential of a solute is evaluated by generating an ensemble of microscopic configurations for the solvent molecules alone. The solute is then superposed onto each configuration and the solute-solvent interaction potential energy calculated to give the probability distribution, Po(AU/kT), illustrated in Figure 3. The excess... [Pg.310]

V. Moulin, A. Schriver, L. Schriver Mazzuoli, and R Chaquin, Infrared spectrum of 2,2,2 trichloroethanol isolated in gas matrices. Ab initio optimization of conformers and potential energy calculations. Chem. Phys. Lett. 263, 423 428 (1996). [Pg.57]

Part 13 of a series, Application of Potential Energy Calculations to Organic Chemistry, from Hokkaido (1). [Pg.117]

The molecular mechanics technique has been called by many different names, including Westheimer method, strain-energy method, conformational energy calculations, empirical potential energy calculations, atom-atom pair potential method, and force field calculations. Empirical force field is widely used, but somewhat long, and many authors omit empirical, leading to confusion with spectroscopic force field calculations. Molecular mechanics (11) now appears to be favored (10a) and is used (abbreviated as MM) throu out this chapter. [Pg.120]

As the final example of the simplified treatment of an aromatic ring, a novel potential energy calculation of a naphthoquinone derivative (36) with a program called EENY will be briefly mentioned (155). This program seems to resemble WMIN in that it calculates only van der Waals energy. The rotation around the cyclopropyl-quinonoid bonds is calculated to have a barrier of about 10 kcal/mol. In this and another case (156), the results could be considerably improved by full relaxation MM calculations. [Pg.140]

Structure-Activity Correlations. The structure-activity relationships of cardenolides have been thoroughly investigated, and have undergone considerable revision on the basis of crystallographic work and potential energy calculations. The correlations are summarized as follows ... [Pg.493]

The computations described briefly in this paper illustrate the interrelationship between the local structure and macroscopic behavior of the DNA helix. Statistical mechanical studies help to identify the most likely morphological arrangements of the polynucleotide backbone and to understand the macroscopic flexibility of the DNA as a whole. Model building and potential energy calculations uncover the detailed local geometries of the chain and clarify the likely pathways between the multitude of allowed spatial forms. [Pg.468]

Fig. 16. Stereo plots of space filling models of the two preferred conformations calculated by a potential energy calculation for the biantennary octasaccharide, p-D-Gal-(l-4)-P-D-Glc.NAc-(l-2)-

Wynn et al. have described a potential energy calculation which utilizes the non bonded interaction and a term for the electrostatic interaction with the inclusion of directed chargers , localized in certain atomic orbitals [192, 193]. With this potential, they obtained for the P-D-glucosyl-ceramide a conformation which is similar to the X-ray crystal structure of P-D-Gal-ceramide [194], The calculation of the a-D-NeuvVAc-(2-3)-P-o-Gal disaccharide shows a conformation with cp-ci = 120° (determined from the stereoplot presented in the publication) which is inconsistent with the data obtained by Sabesan et al. [191], who were able to show that their calculated conformation with (p = 165° is in agreement with NOE data. [Pg.190]

Cj chair form [235]. Potential energy calculations of digitoxigenin-a-L-rhamnoside, digitoxigenin-po-digitoxoside, uzarigenin-oc-L-rhamnoside, and uzarigenin-P-D-6 -deoxyallose showed different minima [236]. [Pg.202]

In a typical analysis of a polymer chain, the experimental values of configuration-dependent properties and their temperature coefficients are compared with the results of rotational isomeric state calculations. These comparisons yield values of the energies for the various rotational states about the backbone bonds, and these conformational preferences can then be used to predict other configuration-dependent properties of the chains. It is also possible to obtain such conformational information from potential energy calculations, using the methods of molecular mechanics.39,46 52... [Pg.27]

Figures 8.3 and 8.4 show potential energy maxima at inter-particle separations of a few nanometres. Surface roughness of at least up to this magnitude is, therefore, unlikely to invalidate these potential energy calculations.

Jaume et al. (1984) studied the contribution of solvent relaxation to the reaction coordinate of the F (H20) + CH3F(H20)SN2 reaction. Potential energy calculations were performed using the ab initio MO method with the 3-21G basis set. The authors found large variation of the solvation parameters along the reaction path and concluded that solvent coordinates are an important part of the reaction coordinate. They showed that the solvent acts not only as a medium for the reaction but also as a rectant. Thus, the solvent does not adjust its position to the changing chemical system but rather takes part in it. [Pg.25]

Figure 2.21. The potential energy calculated at the ab initio CASSCF level illustrating the intersection of the pyramidal and planar surfaces. (Reprinted with permission from Ref. [6].)...

Any potential will predict which structures are impossible, but presumably no potential considered here will be accurate enough to consistently predict which structure is the most stable. Anyway, it is possible in some cases to construct new crystalline phases, and the empirical potential energy calculations indicate the likelihood of the existence of these theoretically predicted phases [63—67],... [Pg.315]

Electrostatic isopotential (EIP) minima186 often identify sites and ease of metabolism by epoxide hydrase, an enzyme responsible for the conversion of epoxides to diols by the addition of water. Molecular electrostatic potential energy calculations also are probably the best means of identifying positions of epoxidation and, possibly, metabolism in general. In the case of aflatoxin B for example, EIP maxima and minima calculated by the CNDO/2 method all lie close to the known sites of metabolism and, in particular, the formation of the carcinogenic 2,3-epoxide is readily predicted.189... [Pg.201]

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