2024-03-28T09:36:38Zhttp://digital.csic.es/dspace-oai/requestoai:digital.csic.es:10261/585642016-08-12T08:58:25Zcom_10261_14181com_10261_4col_10261_14182
Long-range interaction for dimers of atmospheric interest: Dispersion, induction and electrostatic contributions for O2 O2, N2N2 and O 2N2
Bartolomei, Massimiliano
Carmona-Novillo, Estela
Hernández, Marta I.
Campos-Martínez, José
Hernández Lamoneda, Ramón
Electric multipole moments, static dipole polarizabilities, and dynamic dipole, quadrupole, and mixed dipole-octupole polarizabilities of molecular oxygen and nitrogen in their ground electronic states have been obtained by means of high level multiconfigurational ab initio calculations. From these properties, we have obtained electrostatic, dispersion, and induction coefficients for the long-range interactions of the O 2O2, N 2N2, and O 2N2 dimers. Our data is a comprehensive and consistent set that for N2 N2 shows a very good agreement with previous accurate calculations, whereas for quantities involving open-shell O2 represents a considerable improvement over previous estimations. Moreover, the long-range interaction is analyzed and compared for the different interacting partners. It is found that the C8 dispersion interaction plays a nonnegligible role and that the induction component is only important for a detailed description of the highest order anisotropy terms in the spherical harmonics expansion of the long-range potential. It is also found that the total long-range interaction is quite similar in O2 O2 and O2N2, and that differences with N2N2 are mainly because of the important role of the electrostatic interaction in that dimer. Comparison with high level supermolecular calculations indicates that the present long-range potentials are accurate for intermolecular distances larger than about 15 bohr. © 2010 Wiley Periodicals, Inc.
2012-10-22T10:59:42Z
2012-10-22T10:59:42Z
2011
2012-10-22T10:59:43Z
artículo
Journal of Computational Chemistry 32: 279- 290 (2011)
http://hdl.handle.net/10261/58564
10.1002/jcc.21619
eng
closedAccess
John Wiley & Sons