Electron density dictionary (rhoCIF) version 1.0.1
_atom_rho_multipole_coeff_
Names:'_atom_rho_multipole_coeff_Pc' '_atom_rho_multipole_coeff_Pv' '_atom_rho_multipole_coeff_P00' '_atom_rho_multipole_coeff_P10' '_atom_rho_multipole_coeff_P11' '_atom_rho_multipole_coeff_P1-1' '_atom_rho_multipole_coeff_P20' '_atom_rho_multipole_coeff_P21' '_atom_rho_multipole_coeff_P2-1' '_atom_rho_multipole_coeff_P22' '_atom_rho_multipole_coeff_P2-2' '_atom_rho_multipole_coeff_P30' '_atom_rho_multipole_coeff_P31' '_atom_rho_multipole_coeff_P3-1' '_atom_rho_multipole_coeff_P32' '_atom_rho_multipole_coeff_P3-2' '_atom_rho_multipole_coeff_P33' '_atom_rho_multipole_coeff_P3-3' '_atom_rho_multipole_coeff_P40' '_atom_rho_multipole_coeff_P41' '_atom_rho_multipole_coeff_P4-1' '_atom_rho_multipole_coeff_P42' '_atom_rho_multipole_coeff_P4-2' '_atom_rho_multipole_coeff_P43' '_atom_rho_multipole_coeff_P4-3' '_atom_rho_multipole_coeff_P44' '_atom_rho_multipole_coeff_P4-4'
Definition:
Specifies the multipole population coefficients P(l,m) for the atom identified in _atom_rho_multipole_atom_label. The multipoles are defined with respect to the local axes specified in the ATOM_LOCAL_AXES category. The coefficients refer to the multipole formalism described by Hansen & Coppens [1978, equation (2)] which gives the electron density at position vector r with respect to an atomic nucleus as rho(r) = Pc*rho_core(r) + Pv*k^3^*rho_valence(kappa*r) + sum{kappa'(l)^3^*R(kappa'(l),l,r)} *sum{P(l,m)*d(l,m,theta,phi)} where: Pc = _atom_rho_multipole_coeff_Pc Pv = _atom_rho_multipole_coeff_Pv P(0,0) = _atom_rho_multipole_coeff_P00 Pc + Pv + P(0,0) = Z (the atomic number) for a neutral atom kappa = _atom_rho_multipole_kappa, kappa'(l) = _atom_rho_multipole_kappa_prime[l], d(l,m,theta,phi) is the spherical harmonic of order l,m at the position (theta, phi) with respect to spherical coordinates centred on the atom. The summations are performed over the index ranges 0 <= l <= lmax, -l <= m <= l, respectively, where lmax is the highest order of multipole applied. The spherical coordinates are related to the local Cartesian axes defined in category ATOM_LOCAL_AXES, z is the polar axis from which the angle theta is measured, and the angle phi is measured from the x axis in the xy plane with the y axis having a value of phi = +90 degrees. R(kappa'(l),l,r) is defined in the _atom_rho_multipole_radial_* items. rho_core(r) and rho_valence(kappa*r) are the spherical core and valence densities, respectively. They are obtained from atomic orbital analytic wavefunctions such as those tabulated by Clementi & Roetti (1974). They are also the Fourier transforms of the X-ray scattering factors given in _atom_rho_multipole_scat_core and _atom_rho_multipole_scat_valence. Ref: Clementi, E. & Roetti, C. (1974). At. Data Nucl. Data Tables, 14, 177-478. Hansen, N. K. & Coppens, P. (1978). Acta Cryst. A34, 909-921.
Appears in list containing _atom_rho_multipole_atom_label
Type: numb
Category: atom_rho_multipole