Metastable BrO(2+) and NBr(2+) molecules in the gas phase


Autoria(s): AOTO, Yuri Alexandre; OLIVEIRA-FILHO, Antonio Gustavo S. de; FRANZREB, Klaus; ORNELLAS, Fernando R.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/04/2012

19/04/2012

2011

Resumo

The doubly positively charged gas-phase molecules BrO(2+) and NBr(2+) have been produced by prolonged high-current energetic oxygen (17 keV (16)O(-)) ion surface bombardment (ion beam sputtering) of rubidium bromide (RbBr) and of ammonium bromide (NH(4)Br) powdered ionic salt samples, respectively, pressed into indium foil. These novel species were observed at half-integer m/z values in positive ion mass spectra for ion flight times of roughly similar to 12 mu s through a magnetic-sector secondary ion mass spectrometer. Here we present these experimental results and combine them with a detailed theoretical investigation using high level ab initio calculations of the ground states of BrO(2+) and NBr(2+), and a manifold of excited electronic states. NBr(2+) and BrO(2+), in their ground states, are long-lived metastable gas-phase molecules with well depths of 2.73 x 10(4) cm(-1) (3.38 eV) and 1.62 x 10(4) cm(-1) (2.01 eV); their fragmentation channels into two monocations lie 2.31 x 10(3) cm(-1) (0.29 eV) and 2.14 x 10(4) cm(-1) (2.65 eV) below the ground state minimum. The calculated lifetimes for NBr(2+) (v '' < 35) and BrO(2+) (v '' < 18) are large enough to be considered stable against tunneling. For NBr(2+), we predicted R(e) = 3.051 a(0) and omega(e) = 984 cm(-1); for BrO(2+), we obtained 3.033 a(0) and 916 cm(-1), respectively. The adiabatic double ionization energies of BrO and NBr to form metastable BrO(2+) and NBr(2+) are calculated to be 30.73 and 29.08 eV, respectively. The effect of spin-orbit interactions on the low-lying (Lambda + S) states is also discussed. (C) 2011 American Institute of Physics. [doi:10.1063/1.3562121]

National Science Foundation (NSF) [CHE 0111 654]

National Science Foundation NSF[0622775]

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP)

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

Identificador

JOURNAL OF CHEMICAL PHYSICS, v.134, n.10, 2011

0021-9606

http://producao.usp.br/handle/BDPI/16765

10.1063/1.3562121

http://dx.doi.org/10.1063/1.3562121

Idioma(s)

eng

Publicador

AMER INST PHYSICS

Relação

Journal of Chemical Physics

Direitos

openAccess

Copyright AMER INST PHYSICS

Palavras-Chave #CONFIGURATION-INTERACTION CALCULATIONS #GAUSSIAN-BASIS SETS #WAVE-FUNCTIONS #DICATIONS #STATES #REACTIVITY #DYNAMICS #SPECTRUM #IONS #SPIN #Physics, Atomic, Molecular & Chemical
Tipo

article

original article

publishedVersion