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An ab initio study of the HNCN radical.
- Source :
-
Journal of Chemical Physics . 3/1/1994, Vol. 100 Issue 5, p3691. 4p. 1 Diagram, 3 Charts. - Publication Year :
- 1994
-
Abstract
- The equilibrium structure for the ground state of the HNCN radical is calculated at the levels of the self-consistent field theory (SCF), the second-order Mo\ller–Plesset perturbation approximation (MP2), and the full single and double excitation coupled cluster theory including all connected triples in a noniterative manner [CCSD(T)], using various extended basis sets starting from 6–311 G(d,p). At the CCSD(T) level, the outer C–N bond is more than 0.1 Å shorter than the inner one and the N–C–N group departs from linearity by 6°. The total N–C–N length is in good agreement with the experimental value [Herzberg and Warsop, Can. J. Phys. 41, 286 (1963)], however, the H–N–C angle is about 6° smaller. The N–H bond is very close to a normal N–H bond but is about 0.2 Å smaller than the experimental estimate. Except for the smaller H–N–C angle, the geometrical parameters for HNCN closely parallel those for the triplet HCCN molecule. The dipole moment, harmonic frequencies, electric quadrupole, and Fermi contact coupling constants of HNCN are also calculated. The calculated harmonic frequencies confirm the preliminary assignments of Wu, Hall, and Sears [J. Chem. Soc. Faraday Trans. 89, 615 (1993)]. The quadrupole coupling constants for the inner and outer N atoms are comparable, implying a complex pattern of hyperfine split components in the lowest rotational transitions. The present calculation may thus serve as a useful guide for the interpretation of the rotational spectrum. [ABSTRACT FROM AUTHOR]
- Subjects :
- *RADICALS (Chemistry)
*EQUILIBRIUM
*SELF-consistent field theory
Subjects
Details
- Language :
- English
- ISSN :
- 00219606
- Volume :
- 100
- Issue :
- 5
- Database :
- Academic Search Index
- Journal :
- Journal of Chemical Physics
- Publication Type :
- Academic Journal
- Accession number :
- 7618012
- Full Text :
- https://doi.org/10.1063/1.466357