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Coulomb interaction, between two charges

All interionic and almost all intermolecular interactions can be traced to the coulombic interaction between two charges (Section 2.4), and throughout the discussion of intermolecular interactions we shall build on Eq. 5 from Section A, the expression for the potential energy Ef of two charges qx and q1 separated by a distance r ... [Pg.300]

It is worthwhile to examine the Hamiltonian in some detail because it enables one to discuss both intramolecular and intermolecular perturbations from the same point of view. To do so, we start from a zero-order Hamiltonian that contains just the spherical part of the field due to the core (which need not be Coulombic as it includes also the quantum defect [42]) and add two perturbations. U due to external effects and V due to the structure of the core. Here, U contains both the effect of external fields (electrical and, if any, magnetic [1]) and the role of other charges that may be nearby [8, 11, 12, 17]. The technical point is that both the effect of other charges and the effect of the core not being a point charge are accounted for by writing the Coulomb interaction between two charges, at points ri and r2, respectively, as... [Pg.634]

Based on these observations, we can now draw conclusions on the nature and strength of the unscreened Coulomb interactions between two charged carriers in the conduction band, the one centered about an atom or cell located at Rj, and the other centered about Rj ... [Pg.109]

The most important aspect of the dipole-dipole interaction in Eq. (1.2.6) is that the interaction energy changes with distance as whereas the Coulombic interaction between two charges changes with distance as R. In general, the interaction energy... [Pg.14]

The interaction between two charges qi and qj separated by the distance rij in a medium with a dielectric constant e is given by Coulomb s law, which sums the energetic contributions over all pairs ij of point charges within a molecule (Eq. (25)). [Pg.345]

That is, these parameters are represented as classical Coulombic interactions between two pairs of overall electrically neutral charge distributions. For e(i,j) = e(= ) the interaction is between two interpenetrating counter-oriented dipolar distributions. For e(i x j) or e(ijxk) the interaction is between two partially overlapping parallel quadrupolar distributions they seem to be roughly the same size s(- ) for i j k. From the forms here e(- = ) is positive. Presumably e(- ) is positive and larger than... [Pg.64]

The Coulomb interaction between two electrons is reduced by the ability of the other electrons to polarize and shield their charges. Hence, the effective interparticle interaction in Eq. (2-46), i.e., W (r, r2 co), differs from the bare Coulomb interaction. Specifically,... [Pg.35]

The seasoned Debye-Hiickel (D-H) theory, put forth in 1923 [33,34] takes into account the contribution of the ionic electrostatic interactions to the free energy of a solution and provides a quantitative expression for the activity coefficients. The basic concept of the D-H theory is that the long-range Coulomb interaction between two individual ions bathed in a salt solution is mediated by mobile ions from the solution. The effective charges of a certain ion are decreased as the result of charge screening by the mobile counterions it follows that, at sufficient distance, the interaction between two ions decays exponentially. We briefly outline the main considerations and assumptions of the D-H model ... [Pg.7]

We consider a generic donor-acceptor complex solute at infinite dilution in a polyatomic solvent. Both the solute and solvent molecules are represented by rigid and non-polarizable ISM models. In the ISM models the potential energy of interaction between two molecules is a sum of pairwise-additive site-site terms, including Coulombic interactions between partial charges located at the molecular sites. Throughout the paper the subscript A refers to interaction sites of the solute, while the subscript aj refers to interaction site j of solvent molecule a. [Pg.8]

Charge-Charge Interactions (r" ). The energy of interaction between two charges and q2 is given by Coulomb s law ... [Pg.82]

The potential energy of interaction between two charges is related to the force by F = —dV/dr (more generally, F = — VF). Coulomb s law therefore implies... [Pg.177]

According to Coulomb s law, the force of interaction between two charges, qi and q2, separated by a distance, r, is... [Pg.60]

In ion-solid interactions it is convenient to use cgs units rather than SI units in relations involving the charge on the electron. The usefulness of cgs units is clear when considering the Coulomb force between two charged particles with Z, and Zq units of electronic charge separated by a distance r... [Pg.6]

Distance-dependent dielectric constant In computing the Coulomb interaction between two point charges, the dielectric constant is set to the value of the dielectric medium. In an attempt to implicitly simulate water, the dielectric constant should be 80 at long distances, but 1 at close range. Replacing the dielectric constant by r makes the dielectric effect distance-dependent at negligible computational cost. [Pg.753]

The zeroth-order wavefunction yields the first-order perturbation to the energy when combined with the operator V, which describes the interactions between electrons and nuclei on the two different molecules. This first-order correction, known as the Heitler-London interaction energy,may be thought of as consisting of two terms. The first is the classical Coulombic interaction between the charge clouds of the (undistorted) subunits, commonly known as the electrostatic energy, and computed as... [Pg.169]


See other pages where Coulomb interaction, between two charges is mentioned: [Pg.46]    [Pg.336]    [Pg.38]    [Pg.54]    [Pg.43]    [Pg.33]    [Pg.46]    [Pg.336]    [Pg.38]    [Pg.54]    [Pg.43]    [Pg.33]    [Pg.491]    [Pg.202]    [Pg.210]    [Pg.129]    [Pg.12]    [Pg.177]    [Pg.635]    [Pg.157]    [Pg.157]    [Pg.275]    [Pg.91]    [Pg.113]    [Pg.166]    [Pg.676]    [Pg.208]    [Pg.29]    [Pg.285]    [Pg.207]    [Pg.445]    [Pg.1331]    [Pg.210]    [Pg.145]    [Pg.162]    [Pg.159]    [Pg.21]    [Pg.16]    [Pg.12]    [Pg.12]    [Pg.194]   
See also in sourсe #XX -- [ Pg.634 ]




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