Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/164248
Title: Theoretical investigation of the eight low-lying electronic states of the cis- and trans-nitric oxide dimers and its isomerization using multiconfigurational second-order perturbation theory (CASPT2)
Author: Sayós Ortega, Ramón
Valero Montero, Rosendo
Anglada, J. M.
González Pérez, Miguel
Keywords: Radicals (Química)
Isomerització
Teoria del funcional de densitat
Geometria diferencial
Radicals (Chemistry)
Isomerization
Density functionals
Differential geometry
Issue Date: 5-Apr-2000
Publisher: American Institute of Physics
Abstract: In this work we have carried out ab initio electronic structure calculations, CASSCF/CASPT2 and CASSCF/MRCI-SD+Q with several Pople's and correlation-consistent Dunning's basis sets, of the planar cis- and trans-NO dimers for the lowest eight electronic (singlet and triplet) states. The geometry, frequencies, dipole moment, binding energy, and vertical excitation energies are predicted with an accuracy close to or even better than the best reported ab initio previous results for some of these properties, and in very good agreement with the available experimental data. CASPT2 optimized geometries show the existence of at least four shallow NO-dimers (i.e., two cis-(NO)2 (1A1 and 3B2) and two trans-(NO)2 (1Ag and 3Au)), although CASSCF optimization with CASPT2 pointwise calculations indicate the existence of other less stable dimers, on the excited states. Vertical excitation energies were calculated for these four dimers. For the cis-NO dimer, the ordering and the energy spacings between the excited states (i.e., 1A1, 3B2, 1B2, 2nd 1A1, 1A2, 3A2, 3B1, 2nd 3B1) are very similar to those found in a recent MRCI-SD study. The singlet cis-NO dimer (1A1) is the most stable one in almost quantitative accord with the experimental data, and in disagreement with previous density functional theory studies. A nonplanar transition state for the singlet trans ↔ cis isomerization has also been fully characterized. This leads to an almost negligible energy barrier which would originate a rapid isomerization to the most stable cis-NO dimer at low temperatures, in accord with the experimental difficulties to measure the properties of the trans-NO dimer. Not only are basis set superposition error corrections necessary to evaluate accurately the binding energies, but also to determine the NN distance of these symmetrical dimers. Some problems regarding the symmetry of the wave function were found for the symmetrical NO dimers and for the NO+NO asymptote, and several approximate solutions were proposed.
Note: Reproducció del document publicat a: https://doi.org/10.1063/1.481234
It is part of: Journal of Chemical Physics, 2000, vol. 112, p. 6608-6624
URI: http://hdl.handle.net/2445/164248
Related resource: https://doi.org/10.1063/1.481234
ISSN: 0021-9606
Appears in Collections:Articles publicats en revistes (Ciència dels Materials i Química Física)

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