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

2010 | journal article. A publication with affiliation to the University of Göttingen.

Jump to: Cite & Linked | Documents & Media | Details | Version history

Cite this publication

​The benefits of alternation and alkylation: large amplitude hydrogen bond librational modes of alcohol trimers and tetramers​
Larsen, R. W. & Suhm, M. A. ​ (2010) 
Physical Chemistry Chemical Physics12(29) pp. 8152​-8157​.​ DOI: https://doi.org/10.1039/b925578h 

Documents & Media

License

GRO License GRO License

Details

Authors
Larsen, Rene Wugt; Suhm, Martin A. 
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.
Issue Date
2010
Status
published
Publisher
Royal Soc Chemistry
Journal
Physical Chemistry Chemical Physics 
Organization
Institut für Physikalische Chemie 
ISSN
1463-9076

Reference

Citations


Social Media