[en] The calculation of the electric dipole moment of diatomic molecules by the Variational Cellular Method is presented, discussed and compared with the semiempirical CNDO/2 method. The molecule HF is taken as example. It is also shown that the value of the electric dipole moment by the VCM improves considerably when the electronegativity of the atoms of the molecule is taken into account. (Author)

[en] The electric dipole moment of some diatomic molecules is calculated using the Variational Cellular Method. The results obtained for the molecules CO, HB, HF and LiH are compared with other calculations and with experimental data. It is shown that there is strong dependence of the electric dipole moment with respect to the geometry of the cells. It is discussed the possibility of fixing the geometry of the problem by giving the experimental value of the dipole moment. (Author)

[en] A study for main aspects of fast neutron scattering is presented and, a semiclassical approximation applying to several pratic cases is described. The obtained results are compared with experimental data for deformed nuclei, and, with theoretical data based on optical model without treatment of deformations. (M.C.K.)

[en] The process to determine the potential energy curve for diatomic molecules by the Variational Cellular Method is discussed. An analysis of the determination of the electronic eigenenergies and the electrostatic energy of these molecules is made. An explanation of the input data and their meaning is also presented. (Author)

[en] The behavior of the variational celular method with respect to the variation of some input parameters is analysed. The molecules LiH and HF are taken as example in all cases. (author)

[en] Measurements to observe the change in the transmission of nematic liquid crystal with respect to the applied voltage were performed. A theoretical model to explain the oscillatory behavior of the transmission for voltages between 2 and 5 volts and for a cell of 20 μm thick is presented

[en] The one dimensional periodic potential problem is solved using the Laplace transform method and a condensed expression for the relation E x k and effective mass for one electron in a polyatomic structure is determined. Applications related to the effect of the asymmetry of the potential upon the one dimensional band structure are discussed

[en] The results of the calculation, using the Variational Cellular Method (VCM), of the electric dipole moment of several diatomic molecules are improved. In previous calculations, the electronic charge density was treated like a spherically symmetric function in the inscribed sphere within each cell and as being the same constant value for all intercellular regions. Since the results obtained with such an approximation have not been satisfactory, an improved approximation for the charge density in the intercellular regions is needed. It is considered that the charge density is still constant outside the inscribed sphere but with different values in each intercellular region. A new expression for the dipole moment is obtained, and applied to the diatomic molecules HF, CO, BF and CS. In addition, the corresponding dipole moment curves, potential energy curves and spectroscopic constants are calculated taking into consideration our approximation and the traditional approximation for the charge density. The results of the two models are compared with each other and with experimental results for all the molecules considered. (Author)

[en] The electric dipole moment of some diatomic molecules is calculated using the Variational Cellular Method. The results obtained for the CO, HB, HF and LiH molecules are compared with other calculations and with experimental data. It is shown that there is strong dependence of the electric dipole moment with respect to the geometry of the cells. The possibility of fixing the geometry of the problem by giving the experimental value of the dipole moment is discussed. (Author)

[en] A self-consistent calculation based on the Variational Cellular Method is performed on the Cl₂ molecule. The results obtained for the ground state potential curve and the first excited state, the dissociation energy, the molecular orbital energies and other related parameters are compared with other methods of calculations and with available data and the agreement is satisfatory. (Author)