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Covalent bonds in positron dihalides

Abstract

We report a computational study on homo- and heteronuclear e+[X-Y-] compounds formed by two halide anions (X-,Y-= F-,Cl-,Br-) and one positron. Our results indicate the formation of energetically stable positronic molecules in all cases. Analysis of the electron and positron densities points out that the formation of positron covalent bonds underlies the stabilization of the otherwise repelling dihalides, revealing that positronic bonding can reach far beyond the previously addressed e+[H-H-] molecule [Angew. Chem. Int. Ed., 2018,57, 8859-8864.].To a significant extent, the properties of the positron dihalides are similar to those of the purely electronic analogs, e-[A+B+], molecular cations with isoelectronic atomic cores (A+,B+ = Na+, K+, Rb+) bound by one electron. The positron bonds in the e+[X-Y-] complexes are however stronger than those in the isoelectronic e-[A+B+] counterparts, as the former have shorter bond lengths and higher bond energies. While an energy decomposition analysis points out that both electronic and positronic bonds essentially arise from electrostatic interactions, the more stable positron bonds are partly due to the higher polarizabilities of the dihalide anions, and partly to more significant contributions from correlation and relaxation effects.

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Publication details

The article was received on 03 Sep 2019, accepted on 24 Oct 2019 and first published on 29 Oct 2019


Article type: Edge Article
DOI: 10.1039/C9SC04433G
Chem. Sci., 2019, Accepted Manuscript
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    Covalent bonds in positron dihalides

    F. Moncada, L. Pedraza-González, J. A. Charry Martínez, M. T. Varella and A. Reyes, Chem. Sci., 2019, Accepted Manuscript , DOI: 10.1039/C9SC04433G

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