Chiral recognition between 1-(4-fluorophenyl)ethanol and 2-butanol: higher binding energy of homochiral complexes in the gas phase

Literature Information

Publication Date 2010-12-06
DOI 10.1039/C0CP01401J
Impact Factor 3.676
Authors

Alessandra Paladini, Alessandra Ciavardini, Annarita Casavola, Daniele Catone, Mauro Satta, Hans Dieter Barth, Anna Giardini, Maurizio Speranza, Susanna Piccirillo


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Abstract

Diastereomeric adducts between (S)-1-(4-fluorophenyl)-ethanol and R and S 2-butanol, formed by supersonic expansion, have been investigated by means of a combination of mass selected resonant two-photon ionization-spectroscopy and infrared depletion spectroscopy. Chiral recognition is evidenced by the specific spectroscopic signatures of the S1 ← S0 electronic transition as well as different frequencies and intensities of the OH stretch vibrational mode in the ground state. D-DFT calculations have been performed to assist in the analysis of the spectra and the determination of the structures. The homochiral and heterochiral complexes show slight structural differences, in particular in the interaction of the alkyl groups of 2-butanol with the aromatic ring. The experimental results show that the homochiral [FES·BS] complex is more stable than the heterochiral [FES·BR] diastereomer in both the ground and excited states. The binding energy difference has been evaluated to be greater than 0.60 kcal mol−1.

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Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics
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