Quadrupole moment induced

There are higher multipole polarizabilities that describe higher-order multipole moments induced by non-uniform fields. For example, the quadrupole polarizability is a fourth-rank tensor C that characterizes the lowest-order quadrupole moment induced by an applied field gradient. There are also mixed polarizabilities such as the third-rank dipole-quadrupole polarizability tensor A that describes the lowest-order response of the dipole moment to a field gradient and of the quadrupole moment to a dipolar field. All polarizabilities of order higher than dipole depend on the choice of origin. Experimental values are basically restricted to the dipole polarizability and hyperpolarizability [23, 24 and 25]. Ab initio calculations are an important source of both dipole and higher polarizabilities [20] some recent examples include [26, 21]. 

For example the dipole polarizability given in (2.33) has spherical tensor components OQQdl) and a2K(11) The dipole-quadrupole polarizability (A .gY in Cartesian notation), which describes the quadrupole moment induced by an electric field or the dipole moment induced by an electric field gradient, has components 0 (12), 021(02) and 02k(12). The polarizabilities are even (g) or odd (u) under inversion according as 1+1 is even or odd. This information is then sufficient, with the help of Table 3, to determine the transformation properties in the molecular symmetry group. Any component which transforms according to the totally symmetric representation may have a non-zero value. 

Of course there arc other contributors to the value of q besides the valence electrons. Additional effects are due to molecular interactions,22 induced quadrupole moments (Sternheimer, R. M., Phys. Rev. 105, 158, (1957), etc.)... 

Here a designates the trace of the polarizability tensor of one molecule (l/47i o) times the factor of a represents the electric fieldstrength of the quadrupole moment q2. Other non-vanishing multipole moments, for example, octopoles (e.g., of tetrahedral molecules), hexadecapoles (of linear molecules), etc., will similarly interact with the trace or anisotropy of the polarizability of the collisional partner and give rise to further multipole-induced dipole components. 

H2 quadrupole moment, <72(re) at the fixed equilibrium position, and thus the long-range coefficient of the quadrupole-induced dipole component, Eq. 4.3, is about 5% too small relative to the proper vibrational average, <12 = (v = 0 < 2(r) f = 0) [216, 217, 209], A 5% difference of the dipole moment amounts to a 10% difference of the associated spectral intensities. Furthermore, the effects of electron correlation on this long-range coefficient can be estimated. Correlation increases the He polarizability by 5% but decreases the H2 quadrupole moment by 8% [275], a net change of-3% of the leading induction term B R). 

Recent work improved earlier results and considered the effects of electron correlation and vibrational averaging [278], Especially the effects of intra-atomic correlation, which were seen to be significant for rare-gas pairs, have been studied for H2-He pairs and compared with interatomic electron correlation the contributions due to intra- and interatomic correlation are of opposite sign. Localized SCF orbitals were used again to reduce the basis set superposition error. Special care was taken to assure that the supermolecular wavefunctions separate correctly for R —> oo into a product of correlated H2 wavefunctions, and a correlated as well as polarized He wavefunction. At the Cl level, all atomic and molecular properties (polarizability, quadrupole moment) were found to be in agreement with the accurate values to within 1%. Various extensions of the basis set have resulted in variations of the induced dipole moment of less than 1% [279], Table 4.5 shows the computed dipole components, px, pz, as functions of separation, R, orientation (0°, 90°, 45° relative to the internuclear axis), and three vibrational spacings r, in 10-6 a.u. of dipole strength [279]. 

The intermolecular forces of adhesion and cohesion can be loosely classified into three categories quantum mechanical forces, pure electrostatic forces, and polarization forces. Quantum mechanical forces give rise both to covalent bonding and to the exchange interactions that balance tile attractive forces when matter is compressed to the point where outer electron orbits interpenetrate. Pure electrostatic interactions include Coulomb forces between charged ions, permanent dipoles, and quadrupoles. Polarization forces arise from the dipole moments induced in atoms and molecules by the electric fields of nearby charges and other permanent and induced dipoles. 

One of the simplest orientational-dependent potentials that has been used for polar molecules is the Stockmayer potential.48 It consists of a spherically symmetric Lennard-Jones potential plus a term representing the interaction between two point dipoles. This latter term contains the orientational dependence. Carbon monoxide and nitrogen both have permanent quadrupole moments. Therefore, an obvious generalization of Stockmayer potential is a Lennard-Jones potential plus terms involving quadrupole-quadrupole, dipole-dipole interactions. That is, the orientational part of the potential is derived from a multipole expansion of the electrostatic interaction between the charge distributions on two different molecules and only permanent (not induced) multipoles are considered. Further, the expansion is truncated at the quadrupole-quadrupole term. In all of the simulations discussed here, we have used potentials of this type. The components of the intermolecular potentials we considered are given by ... 

The quantity on the left is the Fourier component of the dipole moment induced by the optical field Max(w). These equations can be generalized to mixed frequency-dependent electric dipole, electric quadrupole, magnetic dipole properties, and similar equations can be written for the Fourier components of the permanent electric quadrupole, aj8(magnetic dipole, ma(co). For static Maxwell fields similar expansions yield effective (starred) properties, defined as derivatives of the electrostatic free energies. 

It is interesting to note that in the quadrupole relaxation process discussed in Section 3.4 (Fig. 12) the core hole can be regarded as fluctuating between the different degenerate orbital magnetic sublevels. In this way, the core hole can form a static quadrupole moment and induce a quadrupole screening charge distribution. 

The calculated first hyperpolarizabilities (see Table 2-4) are surprisingly close to the experimental data, which is probably fortuitous because they were calculated without taking into account vibrational effect. These studies demonstrated also that the double-zeta basis set augmented by field-induced polarization functions, although sufficient for calculations of dipole and quadrupole moments of the studied molecules at the Kohn-Sham LDA level, is not sufficient in the case of hyperpolarizabilities. 

Bersohn 76) has calculated the crystal field created by the molecular dipoles in the lattice of CH3C1. The static dipole moment of the molecules induces through the polarizability of the molecules an additional dipole moment which increases the dipole moment of the free molecule by a factor of about 1.05. This in turn means that the C—Cl bond has increased in ionic character under the influence of the intermolecular electric fields and therefore (see Eq. (II.9 the quadrupole coupling constant will be lower relative to the gaseous state. Besides the dipole moment induced in the direction of the static dipole, a perpendicular partial moment should be induced, too. Therefore the axial symmetry of the C—Cl bond will be disturbed and the asymmetry parameter 77 may become unequal zero. A small asymmetry parameter 17 = 0.028 has been observed for the nuclear quadrupole interaction in solid CH3I. Bersohn also calculated from the known crystal structure of 1,3,5-trichlorobenzene the induced... 

For an absolute agreement between the observed and calculated crystal field effects in such dipolar crystal lattices, the zero point vibrations have to be considered, as Bersohn pointed out. Furthermore, we think that the part of the solid state shift is due to the contribution of the quadrupole polarization (antishielding factor). The inner shell electrons of the atom considered experience an induced quadrupole moment under the influence of the external fields. This... 

Spin relaxation in a nucleus is induced by random fluctuations of local magnetic fields. These result from time-dependent modulation of the coupling energy of the resonating nuclear spin with nearby nuclear spins, electron spins, quadrupole moments, etc. Any time-dependent phenomenon able to modulate these couplings can contribute to nuclear relaxation. The distribution of the frequencies contained in these time-dependent phenomena is described by a correlation function, characterized by a parameter Tc, the correlation time. Its reciprocal can be considered as the maximum frequency produced by the fluctuations in the vicinity of the nuclear spin. If more than one process modulates the coupling between the nuclear spin and its surroundings, the reciprocal of the effective correlation time is the sum of the reciprocals of the various contributions... 

To further illustrate the importance of coupling the electrostatic and short-ranged repulsion interactions, we consider the example of a dimer of polarizable rare gas atoms, as presented by Jordan et al. In the absence of an external electric field, a PPD model predicts that no induced dipoles exist (see Eq. [12]). But the shell model correctly predicts that the rare gas atoms polarize each other when displaced away from the minimum-energy (force-free) configuration. The dimer will have a positive quadrupole moment at large separations, due to the attraction of each electron cloud for the opposite nucleus, and a negative quadrupole at small separations, due to the exchange-correlation repulsion of the electron clouds. This result is in accord with ab initio quantum calculations on the system, and these calculations can even be used to help parameterize the model. ... 

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