New structures of hydronium cation clusters.

C R Chim

Hunter College & the Graduate Center, City University of New York, New York, NY 10065, USA.

Published: August 2012

Four new hydronium ion structures are investigated by means of quantum mechanical calculations at the DFT/B3LYP6-311+G(2d,2p) level of theory. There exist experimental crystallographic hydronium cations (HO ) of two different geometrical structures, one BEXFEQ (acyclic) and one IYEPEH (cyclic). Molecular calculations reveal their relative stability. Another hydronium cation NEBDII (HO ) when optimized reveals a totally new and unexpected structure. All three optimized structures are shown to be quite stable as judged by their binding energies, and therefore may possibly be found in solution. A main result of this article is the discovery of three new optimized structures of hydronium ions, all of which are preferentially ring structures. The optimized structure of HO is a cube lacking a vertex. Putting a water molecule at the "empty" vertex leads by energy optimization to a structure of HO which has the approximate symmetry of a cube. This cubic structure, as judged by its fragments, is one of the most interesting of the hydronium ions studied in this paper. The addition of HO to a group of seven neutral molecules in the hypothetical reaction HO + 7 HO → HO induces two water molecules to each capture a proton at the expense of two other water molecules (converting them into hydroxyl anions) leading to a cluster with the formula , where the superscripts are the integrated QTAIM atomic charges (in atomic units) on the respective species (inside the bracket) or on groups of a given species (outside the bracket). The cubic arrangement of 3HO.3HO.2OH is accompanied with a significant redistribution of charge: Each hydronium cation carries +0.7 au, the hydroxyl anions only around -0.6 au each, while the water molecules remain quasi-neutral with a slight positive charge.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6557462PMC
http://dx.doi.org/10.1016/j.crci.2012.04.010DOI Listing

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