Issue 38, 2016

Structures and spectroscopy of protonated ammonia clusters at different temperatures

Abstract

The accurate determination of the solvation energies of a proton in ammonia is based on the precise knowledge of the structures of neutral and protonated ammonia clusters. In this work, we have investigated all the possible and stable structures of protonated ammonia clusters H+(NH3)n=2–9, along with their isomeric distribution at a specific temperature. New significant isomers are reported here for the first time and show that the structures of protonated ammonia clusters are not only branched linear as assumed by all previous authors. Branched linear structures are the only ones responsible for the population of protonated ammonia clusters for n = 4–6 at any temperature. However, for larger cluster sizes, these types of structures compete with branched cyclic, double cyclic, branched double cyclic and triple cyclic structures depending on the temperature. In addition, we have shown that protonated ammonia clusters are all Eigen structures and the first solvation shell of the related ammonium ion core is saturated by four ammonia molecules. We have also carried out a study of the hydrogen bond network of protonated ammonia clusters establishing the stability rule governing the various isomers of each cluster from estimated energies of the hydrogen bond types in H+(NH3)n=2–9. With all these results, a route for the accurate determination of the solvation energies of a proton in ammonia at a given temperature could be conceivable.

Graphical abstract: Structures and spectroscopy of protonated ammonia clusters at different temperatures

Supplementary files

Article information

Article type
Paper
Submitted
12 May 2016
Accepted
05 Sep 2016
First published
06 Sep 2016

Phys. Chem. Chem. Phys., 2016,18, 26827-26843

Structures and spectroscopy of protonated ammonia clusters at different temperatures

A. Malloum, J. J. Fifen, Z. Dhaouadi, S. G. Nana Engo and N. Jaidane, Phys. Chem. Chem. Phys., 2016, 18, 26827 DOI: 10.1039/C6CP03240K

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