Issue 9, 2011

Comment on “Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid” by R. Tonner, V. A. Soloshonok and P. Schwerdtfeger, Phys. Chem. Chem. Phys., 2011, 13, 811-817

Abstract

It is argued that differences between homo- and heterochiral dimers of the title compound in the gas phase cannot be responsible for the different sublimation behaviour of racemic and enantiomerically pure crystals near room temperature.

Graphical abstract: Comment on “Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid” by R. Tonner, V. A. Soloshonok and P. Schwerdtfeger, Phys. Chem. Chem. Phys., 2011, 13, 811-817

Article information

Article type
Comment
Submitted
08 Nov 2010
Accepted
10 Jan 2011
First published
24 Jan 2011

Phys. Chem. Chem. Phys., 2011,13, 4159-4160

Comment on “Theoretical investigations into the enantiomeric and racemic forms of α-(trifluoromethyl)lactic acid” by R. Tonner, V. A. Soloshonok and P. Schwerdtfeger, Phys. Chem. Chem. Phys., 2011, 13, 811-817

M. A. Suhm and M. Albrecht, Phys. Chem. Chem. Phys., 2011, 13, 4159 DOI: 10.1039/C0CP02455D

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