These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Search MEDLINE/PubMed

  • Title: Ab initio calculations on low-lying electronic states of SnCl(2)- and Franck-Condon simulation of its photodetachment spectrum.
    Author: Lee EP, Dyke JM, Mok DK, Chow WK, Chau FT.
    Journal: Phys Chem Chem Phys; 2008 Feb 14; 10(6):834-43. PubMed ID: 18231686.
    Abstract:
    Geometry optimization and harmonic vibrational frequency calculations have been carried out on low-lying doublet and quartet electronic states of stannous (tin(II)) dichloride anion (SnCl(2)(-)) employing the CASSCF and RCCSD(T) methods. The small-core fully-relativistic effective core potential, ECP28MDF, was used for Sn in these calculations, together with valence basis sets of up to augmented correlation-consistent polarized-valence quintuple-zeta (aug-cc-pV5Z) quality. The ground electronic state of SnCl(2)(-) is determined to be the X(2)B(1) state, with the A(2)B(2) and ã(4)Sigma state, calculated to be ca. 1.50 and 2.72 eV higher in energy respectively. The electron affinities of the X(1)A(1) and ã(3)B(1) states of SnCl(2) have been computed to be 1.568+/-0.007 and 4.458+/-0.002 eV respectively, including contributions of core correlation and extrapolation to the complete basis set limit. The SnCl(2) (X(1)A(1)) + e <-- SnCl(2)(-) (X(2)B(1)) and SnCl(2) (ã(3)B(1)) + e <-- SnCl(2)(-) (X(2)B(1)) photodetachment bands have been simulated with computed Franck-Condon factors, which include an allowance for anharmonicity and Duschinsky rotation.
    [Abstract] [Full Text] [Related] [New Search]