Reported here are measurements of the rotational spectra of two isotopologues (35Cl and 37Cl) of one of the simplest chiral carboxylic acids, 2-chloro-propionic acid. The spectra have been obtained in a supersonic expansion, using free-jet millimeter-wave direct-absorption as well as pulsed-jet FT microwave Spectroscopies. A single conformer has been detected, characterized by a methyl group nearly cis with respect to the carbonylic oxygen. Within the realm of chiral recognition, the relative simplicity of the observed spectrum should allow for the detection of the microwave spectrum of the polar homo-dimer.
Conformation of chiral molecules: the rotational spectrum of 2-chloropropionic acid / A.Lesarri; J.-U.Grabow; W.Caminati. - In: CHEMICAL PHYSICS LETTERS. - ISSN 0009-2614. - STAMPA. - 468:(2009), pp. 18-22. [10.1016/j.cplett.2008.11.053]
Conformation of chiral molecules: the rotational spectrum of 2-chloropropionic acid
CAMINATI, WALTHER
2009
Abstract
Reported here are measurements of the rotational spectra of two isotopologues (35Cl and 37Cl) of one of the simplest chiral carboxylic acids, 2-chloro-propionic acid. The spectra have been obtained in a supersonic expansion, using free-jet millimeter-wave direct-absorption as well as pulsed-jet FT microwave Spectroscopies. A single conformer has been detected, characterized by a methyl group nearly cis with respect to the carbonylic oxygen. Within the realm of chiral recognition, the relative simplicity of the observed spectrum should allow for the detection of the microwave spectrum of the polar homo-dimer.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.