First Principle Attempt towards the Thermodynamic Stability of Telluroformaldehyde and its Heavier Analogs: H(2-n)X(n)A=Te (X=H, F, Cl and Br; A=C, Si and Ge; n=0-2)

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Abstract

H(2-n)X(n)A=Te (X=H, F, Cl and Br; A=C, Si and Ge; n=0-2), the novel heavy congeners of formaldehyde, have been studied in the gas phase using MP2/def2-TVZP and BP86/def2-TVZP methods. Emphasis has been laid on the bond strengths and the standard heats of formation (ΔHf°) of the mentioned telluro-ketones to reveal their thermodynamic stabilities and further assist in their isolations. The bond strengths have been evaluated in terms of the σ-bond energy, π-bond energy and the bond dissociation enthalpy, D°, using isodesmic reaction schemes. The methodology employed has satisfactorily reproduced the bond strengths and the ΔHf° of formaldehyde and silanone. The findings from this work indicate that the D° of the F2A=Te (A=C, Si and Ge) molecules are comparable to that of H2C=O and thus their respective stabilities are expected to be equivalent to that of formaldehyde. Besides, the fluorinated telluro-ketones are predicted to possess a unique thermodynamic stability since they have the most exothermic ΔHf° in their respective series while the H2A=Te ketones have the most endothermic ΔHf°. In addition, the silanetellones are found to be thermodynamically more stable than their corresponding telluroformaldehyde and germanetellone analogs. Since reported data for H(2-n)X(n)A=Te (X=H, F, Cl and Br; A=C, Si and Ge; n=0-2) is non-existent in terms of the thermodynamic data, the findings of this work should supplement the literature with reliable information.

Keywords

Telluro-ketones
Formaldehyde
Silanone
Germanone
Molecular structure
Bond-strength
Bond-dissociation enthalpy
NBO analysis
Standard heat of formation

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Selection and peer review under responsibility of the organizers of the 2013 International Conference on Computational Science.