| Texto completo | |
| Autor(es): |
Moncada, Felix
[1]
;
Pedraza-Gonzalez, Laura
[1]
;
Charry, Jorge
[1]
;
Varella, Marcio T. do N.
[2]
;
Reyes, Andres
[1]
Número total de Autores: 5
|
| Afiliação do(s) autor(es): | [1] Univ Nacl Colombia, Dept Chem, Av Cra 30 45-03, Bogota - Colombia
[2] Univ Sao Paulo, Inst Fis, Rua Matao 1731, BR-05508090 Sao Paulo, SP - Brazil
Número total de Afiliações: 2
|
| Tipo de documento: | Artigo Científico |
| Fonte: | CHEMICAL SCIENCE; v. 11, n. 1, p. 44-52, JAN 7 2020. |
| Citações Web of Science: | 0 |
| Resumo | |
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 {[}J. Charry, M. T. do N. Varella and A. Reyes, 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. (AU) | |
| Processo FAPESP: | 17/24145-9 - Transientes moleculares aniônicos e positrônicos |
| Beneficiário: | Andre de Pinho Vieira |
| Modalidade de apoio: | Auxílio à Pesquisa - Regular |