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Spectroscopic study of the benchmark Mn+-H2 complex
Faculty of Science - Papers (Archive)
  • Viktoras Dryza, University Of Melbourne
  • Berwyck L. J Poad, University of Wollongong
  • Evan J Bieske, University Of Melbourne
RIS ID
72099
Publication Date
1-1-2009
Publication Details

Dryza, V., Poad, B. L. J. & Bieske, E. J. (2009). Spectroscopic study of the benchmark Mn+-H2 complex. Journal of Physical Chemistry A, 113 (21), 6044-6048.

Abstract
We have recorded the rotationally resolved infrared spectrum of the weakly bound Mn+-H2 complex in the H-H stretch region (4022-4078 cm(-1)) by monitoring Mn+ photodissociation products. The band center of Mn+-H2, the H-H stretch transition, is shifted by -111.8 cm(-1) from the transition of the free H2 molecule. The spectroscopic data suggest that the Mn+-H2 complex consists of a slightly perturbed H2 molecule attached to the Mn+ ion in a T-shaped configuration with a vibrationally averaged intermolecular separation of 2.73 A. Together with the measured Mn+...H2 binding energy of 7.9 kJ/mol (Weis, P.; et al. J. Phys. Chem. A 1997, 101, 2809.), the spectroscopic parameters establish Mn+-H2 as the most thoroughly characterized transition-metal cation-dihydrogen complex and a benchmark for calibrating quantum chemical calculations on noncovalent systems involving open d-shell configurations. Such systems are of possible importance for hydrogen storage applications.
Citation Information
Viktoras Dryza, Berwyck L. J Poad and Evan J Bieske. "Spectroscopic study of the benchmark Mn+-H2 complex" (2009) p. 6044 - 6048
Available at: http://works.bepress.com/berwyck_poad/1/