Abstract
Heats of formation have been determined for the tin−oxygen compounds SnO, SnO2, H2SnO, and H3SnOH by ab initio computations of reaction energies for isogyric reactions. The electronic structure methods employed include the coupled-cluster singles and doubles method with a perturbative correction for connected triple substitutions [CCSD(T)] and the Brueckner doubles method with analogous corrections for triple and quadruple substitutions [BD(TQ)]. Correlation-consistent triple- and quadruple-ζ basis sets were employed in conjunction with a large-core pseudopotential and a core polarization potential for Sn, and a basis set incompleteness correction was computed from extrapolations to the infinite basis set limit. Values of 9 ± 4, 10 ± 4, 34 ± 4, and −20 ± 4 kcal mol-1 are proposed for for SnO, SnO2, H2SnO, and H3SnOH, respectively. Polynomial fits were carried out for the heat capacity and the standard enthalpy and entropy over the 300−3100 K temperature range.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.