12136-26-4Relevant articles and documents
Electron spin resonance matrix isolation studies of 27Al16,17O, 69,71Ga16,17O and 115In16,17O: Observed hyperfine interactions compared with ab initio theoretical results
Knight Jr., Lon B.,Kirk, Thomas J.,Herlong, John,Kaup, John G.,Davidson
, p. 7011 - 7019 (2007/10/03)
Electron spin resonance (ESR) studies are reported for Al16,17O, Ga16,17O, and In16,17O isolated in neon matrices at 4 K. Except for Al16O, no previous ESR measurements have been reported for these X 2Σ diatomic radicals. The pulsed laser vaporization of the metals in the presence of 16O2 and 17O2 produced high quality ESR spectra of these metal oxide radicals whose nuclear hyperfine interactions (A tensors) were fully resolved for both the metal and oxygen nuclei. An analysis of the experimental spin densities in combination with different types of theoretical calculations provided detailed information concerning the electronic structure trends going down this metal oxide group. Increased p-orbital spin density on oxygen was observed for the heavier metal oxide radicals. Nonrelativistic ab initio calculations with an extended basis set and the UB3LYP method reproduced the trends in the isotropic and dipolar hyperfine interactions. All-electron CI calculations, restricted open-shell Hartree-Fock (ROHF) wave functions, and unrestricted Hartree-Fock wave functions gave results very different from experiment and from each other for the isotropic interaction. All calculations were in fair agreement with each other for the dipolar interaction and provided an assignment of the sign for that term.
MATRIX-ISOLATION STUDIES BY ELECTRONIC SPECTROSCOPY OF GROUP IIIA METAL-WATER PHOTOCHEMISTRY
Douglas, Monte A.,Hauge, Robert H.,Margrave, John L.
, p. 1533 - 1554 (2007/10/02)
This paper reports an investigation of the electronic structures of the Group IIIA metal atom hydration reaction intermediates (MOH2 adducts) and their subsequent photolysis products (HMOH, MOH and MO) where M = Al, Ga and In.The metal-water interaction in the adduct is sufficiently strong to perturb the electronic structure of the metal atom; consequently, one observes a unique band structure for the adduct that is red shifted from the metal's atomic resonance transition.Molecular orbital and electronic state-to-state correlations are presented.
