Document Type

Article

Original Publication Date

2009

Journal/Book/Conference Title

The Journal of Chemical Physics

Volume

131

Issue

12

DOI of Original Publication

10.1063/1.3234363

Comments

Originally published at http://dx.doi.org/10.1063/1.3234363

Date of Submission

October 2015

Abstract

Using a combination of anion photoelectron spectroscopy and density functional theory calculations, we explored the influence of the shell model on H atom site selectivity in Al13H−. Photoelectron spectra revealed that Al13H− has two anionic isomers and for both of them provided vertical detachment energies (VDEs). Theoretical calculations found that the structures of these anionic isomers differ by the position of the hydrogen atom. In one, the hydrogen atom is radially bonded, while in the other, hydrogen caps a triangular face. VDEs for both anionic isomers as well as other energetic relationships were also calculated. Comparison of the measured versus calculated VDE values permitted the structure of each isomer to be confirmed and correlated with its observed photoelectron spectrum. Shell model, electron-counting considerations correctly predicted the relative stabilities of the anionic isomers and identified the stable structure of neutral Al13H.

Rights

Grubisic, A., Li, X., Stokes, S. T., et al. Al13H−: Hydrogen atom site selectivity and the shell model. The Journal of Chemical Physics 131, 121103 (2009). Copyright © 2009 AIP Publishing LLC.

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