Issue 29, 2010

The benefits of alternation and alkylation: large amplitude hydrogen bond librational modes of alcohol trimers and tetramers

Abstract

Intermolecular hydrogen bond librational modes in cyclic trimers and tetramers of methanol and t-butyl alcohol isolated at low temperature in pulsed supersonic jet expansions are observed by direct absorption spectroscopy in the far-infrared region. The large amplitude librational modes probe the strength and directionality of the intermolecular hydrogen bonds. In addition, their frequency and intensity is very sensitive to the angle which the alkyl groups form with the hydrogen bonded ring. Theoretical predictions which fail to describe the trends in cluster size, alkylation and symmetry splitting reported in this work are likely to miss important ingredients of the underlying intermolecular interaction. Analysis of the vibrational correlation diagram between planar and puckered tetramer structures circumvents some deficiencies of approximate treatments.

Graphical abstract: The benefits of alternation and alkylation: large amplitude hydrogen bond librational modes of alcohol trimers and tetramers

Supplementary files

Article information

Article type
Paper
Submitted
04 Dec 2009
Accepted
21 Jan 2010
First published
16 Feb 2010

Phys. Chem. Chem. Phys., 2010,12, 8152-8157

The benefits of alternation and alkylation: large amplitude hydrogen bond librational modes of alcohol trimers and tetramers

R. Wugt Larsen and M. A. Suhm, Phys. Chem. Chem. Phys., 2010, 12, 8152 DOI: 10.1039/B925578H

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