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The surprising metastability of TeH2+.
de Oliveira-Filho, Antonio G S; Ornellas, Fernando R.
Afiliação
  • de Oliveira-Filho AG; Departamento de Química Fundamental, Instituto de Química, Universidade de São Paulo, Av. Prof. Lineu Prestes, 748, São Paulo, São Paulo 05508-000, Brazil.
J Chem Phys ; 138(22): 224309, 2013 Jun 14.
Article em En | MEDLINE | ID: mdl-23781797
A high-level ab initio investigation of a manifold of electronic states of the diatomic dication TeH(2+) is presented. Potential energy curves for both Λ + S and relativistic (Ω) states are constructed not only making evident the metastability of this system, but also the large energy splitting due to spin-orbit interactions. This effect is also very significant in the region close to the crossing of the (2)Π and (4)Σ(-) states, where avoided crossings between the Ω states have a relatively large impact on the height of the energy barriers. In contrast to TeH, with only two bound states (X1 (2)Π3∕2 and X2 (2)Π1∕2) below about 25,000 cm(-1), in the case of TeH(2+) a much richer energy profile is obtained indicating various possibilities of electronic transitions. Guided by the results of this study, the experimental characterization of these states is now a challenge to spectroscopists. Since close to the equilibrium region the double positive charge is centered on the tellurium atom, the binding in this system can be rationalized as a simple covalent bond between the pz and s orbitals of Te(2+) and H, respectively. As the internuclear distance increases, the electron affinity of Te(2+) overcomes that of H(+) and the system dissociates into two singly charged fragments. A simulation of the double ionization spectra complements the characterization of the electronic states, and results of a mass spectrometric investigation corroborates the predicted transient existence of this metastable species.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Chem Phys Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Brasil País de publicação: Estados Unidos