posted on 2016-11-17, 10:29authored byAhmed M. Sadoon, Gautam Sarma, Ethan M. Cunningham, Jon Tandy, M. W. Hanson-Heine, N. A. Besley, Shengfu Yang, Andrew M. Ellis
Infrared (IR) spectra of complexes between NaCl and methanol have been recorded for the first time. These complexes were formed in liquid helium nanodroplets by consecutive pick-up of NaCl and CH3OH molecules. For the smallest NaCl(CH3OH)n, complexes where n = 1-3, the IR data suggest that the lowest-energy isomer is the primary product in each case. The predominant contribution to the binding comes from ionic hydrogen bonds between the OH in each methanol molecule and the chloride ion in the NaCl, as established by the large red shift of the OH stretching bands compared with the isolated CH3OH molecule. For n ≥ 4, there is a dramatic shift from discrete vibrational bands to very broad absorption envelopes, suggesting a profound change in the structural landscape and, in particular, access to multiple low-energy isomers.
Funding
The authors are grateful to the Leverhulme Trust (RPG-2012-
740) and the UK Engineering and Physical Sciences Research
Council (EP/L50502X/1) for grants in aid of this work.
Support from the University of Nottingham for access to its
High-Performance Computing facility and the Ministry of
Higher Education and Scientific Research in Iraq for a Ph.D.
studentship for A.M.S. are also gratefully acknowledged.
History
Citation
Journal of Physical Chemistry A. 2016, 120 (41), pp 8085–8092
Author affiliation
/Organisation/COLLEGE OF SCIENCE AND ENGINEERING/Department of Chemistry
The Supporting Information is available free of charge on the
ACS Publications website at DOI: 10.1021/acs.jpca.6b06227.
Calculated vibrational frequencies and IR absorption line
strengths and the IR spectrum recorded in the m/z 23
mass channel (PDF)