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Issue 32, 2007
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A peptide co-solvent under scrutiny: self-aggregation of 2,2,2-trifluoroethanol

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Abstract

Trifluoroethanol (TFE) and its aggregates are studied via supersonic jet FTIR and Raman spectroscopy as well as by quantum chemistry and simple force field approaches. A multi-slit nozzle is introduced to study collisionally excited clusters. Efforts are made to extract harmonic frequencies from experiment for better comparison to theory. Based on deuteration, the OH stretching anharmonicity changes weakly upon dimerization, but increases for trimers. Among the possible dimer conformations, only an all-gauche, homoconfigurational, compact, OH–F connected structure is observed in an extreme case of chiral discrimination. Quantum tunneling assisted pathways for this surprising helicity synchronization are postulated. The oscillator coupling in hydrogen-bonded trimers is analyzed. Trans conformations of TFE start to become important for trimers and probably persist in the liquid state. Simple force fields can be refined to capture some molecular recognition features of TFE dimer, but their limitations are emphasized.

Graphical abstract: A peptide co-solvent under scrutiny: self-aggregation of 2,2,2-trifluoroethanol

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Article information


Submitted
11 Apr 2007
Accepted
17 May 2007
First published
18 Jun 2007

Phys. Chem. Chem. Phys., 2007,9, 4472-4490
Article type
Paper

A peptide co-solvent under scrutiny: self-aggregation of 2,2,2-trifluoroethanol

T. Scharge, C. Cézard, P. Zielke, A. Schütz, C. Emmeluth and M. A. Suhm, Phys. Chem. Chem. Phys., 2007, 9, 4472
DOI: 10.1039/B705498J

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