Classically a chiral molecule and its enantiomer have been considered energetically equivalent:<ΨDHpcΨD>=<ΨLP−1HpcPΨL>=<ΨLHpcΨL>as the parity-conserving hamiltonian Hpc does not change under the transformation P−1 HpcP, where P is the parity operator which transforms the wavefunction of one enantiomer into the other. However the parity-violating weak interactions ensure that this equivalence is no longer exact.

On the stabilization of natural L-alpha-amino acids and D-sugars via parity-violating effects / Lazzeretti, Paolo; Ligabue, Andrea; A., Soncini; R., Zanasi. - STAMPA. - (1999), pp. 377-386.

On the stabilization of natural L-alpha-amino acids and D-sugars via parity-violating effects.

LAZZERETTI, Paolo;LIGABUE, Andrea;
1999

Abstract

Classically a chiral molecule and its enantiomer have been considered energetically equivalent:<ΨDHpcΨD>=<ΨLP−1HpcPΨL>=<ΨLHpcΨL>as the parity-conserving hamiltonian Hpc does not change under the transformation P−1 HpcP, where P is the parity operator which transforms the wavefunction of one enantiomer into the other. However the parity-violating weak interactions ensure that this equivalence is no longer exact.
``ADVANCES IN BIOCHIRALITY''
9780080434049
Elsevier
PAESI BASSI
On the stabilization of natural L-alpha-amino acids and D-sugars via parity-violating effects / Lazzeretti, Paolo; Ligabue, Andrea; A., Soncini; R., Zanasi. - STAMPA. - (1999), pp. 377-386.
Lazzeretti, Paolo; Ligabue, Andrea; A., Soncini; R., Zanasi
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/11380/462014
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