Phenylacetylene as a gas phase sliding balance for solvating alcohols
Author:
Affiliation:
1. Institut für Physikalische Chemie
2. Georg-August-Universität Göttingen
3. 37077 Göttingen
4. Germany
Abstract
The preferred OH docking site in phenylacetylene can be controlled by chemical tuning between phenyl and acetylenic OH⋯π
Funder
Deutsche Forschungsgemeinschaft
Georg-August-Universität Göttingen
Publisher
Royal Society of Chemistry (RSC)
Subject
Physical and Theoretical Chemistry,General Physics and Astronomy
Link
http://pubs.rsc.org/en/content/articlepdf/2019/CP/C9CP00435A
Reference40 articles.
1. Structure of the Phenylacetylene−Water Complex as Revealed by Infrared-Ultraviolet Double Resonance Spectroscopy
2. IR−UV Double Resonance Spectroscopic Investigation of Phenylacetylene−Alcohol Complexes. Alkyl Group Induced Hydrogen Bond Switching
3. Hydrogen-Bonded Complexes of Phenylacetylene with Water, Methanol, Ammonia, and Methylamine. The Origin of Methyl Group-Induced Hydrogen Bond Switching
4. Phenylacetylene: A Hydrogen Bonding Chameleon
5. A π-stacked phenylacetylene dimer
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