.It is shown via extended numerical tests that the ab initio calculation of a parity-violating energy term, at the random-phase approximation (or coupled Hartree-Fock perturbation theory) level of accuracy, gives results which are more than one order of magnitude larger than those usually obtained by means of less accurate methods employed so far. These findings make more plausible the hypothesis of electroweak selection of natural enantiomers.

On the Calculation of Parity-Violating Energies in Hydrogen Peroxide and Hydrogen Disulphide Molecules within the Random-Phase Approximation / Lazzeretti, Paolo; R., Zanasi. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - STAMPA. - 279:(1997), pp. 349-354. [10.1016/S0009-2614(97)01060-9]

On the Calculation of Parity-Violating Energies in Hydrogen Peroxide and Hydrogen Disulphide Molecules within the Random-Phase Approximation

LAZZERETTI, Paolo;
1997

Abstract

.It is shown via extended numerical tests that the ab initio calculation of a parity-violating energy term, at the random-phase approximation (or coupled Hartree-Fock perturbation theory) level of accuracy, gives results which are more than one order of magnitude larger than those usually obtained by means of less accurate methods employed so far. These findings make more plausible the hypothesis of electroweak selection of natural enantiomers.
279
349
354
On the Calculation of Parity-Violating Energies in Hydrogen Peroxide and Hydrogen Disulphide Molecules within the Random-Phase Approximation / Lazzeretti, Paolo; R., Zanasi. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - STAMPA. - 279:(1997), pp. 349-354. [10.1016/S0009-2614(97)01060-9]
Lazzeretti, Paolo; R., Zanasi
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11380/454433
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