Issue 40, 2006

Quantitative chirality synchronization in trifluoroethanol dimers

Abstract

2,2,2-Trifluoroethanol molecules synchronize their transiently chiral gauche configurations upon dimerization in supersonic jet expansions, while they avoid an energetically competitive heteroconfigurational hydrogen bonded dimer topology predicted by extensive quantum chemical calculations.

Graphical abstract: Quantitative chirality synchronization in trifluoroethanol dimers

Article information

Article type
Communication
Submitted
12 Jul 2006
Accepted
05 Sep 2006
First published
21 Sep 2006

Phys. Chem. Chem. Phys., 2006,8, 4664-4667

Quantitative chirality synchronization in trifluoroethanol dimers

T. Scharge, T. Häber and M. A. Suhm, Phys. Chem. Chem. Phys., 2006, 8, 4664 DOI: 10.1039/B609868A

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