Density functional calculations (B3LYP) on IrXH(2)(eta(2)-H(2))(PR(3))(2) for X = Cl, Br, I and R = H, Me and inelastic neutron scattering studies for X = Cl, Br, I and R = Pr(i) are used to elucidate the mechanisms for the intramolecular dihydrogen/hydride exchange. The two lowest energy processes are rotation of the dihydrogen ligand and oxidative addition of the dihydrogen to form an intermediate Ir(V) tetrahydride, which undergoes rapid reductive elimination to interchange the dihydrides and the dihydrogen. The use of PMe(3) as a model phosphine is essential to bring the calculated barriers for the dihydrogen/hydride interchange into agreement with the experimental observations. The activation energy for site exchange (1.9 kcal/mol) is found to be in excellent agreement with the experimental result obtained for X = Cl (1.5(2) kcal/mol), and the calculations show a slight decrease in this value from X = C1 to I. Comparison between calculated rotational barriers (0.3 to 0.7 kcal/mol) and experimental values obtained for IrXH(2)(eta(2)-H(2))(PR(3))(2) (X = Cl, Br, I; R = Pr(i)) (0.5 to 1.0 kcal/mol) also demonstrates that the quantitative estimate of the barrier to rotation requires PMe(3) as the minimal model ligand.

Transition metal polyhydride complexes. 10. Intramolecular hydrogen exchange in the octahedral iridium(III) dihydrogen dihydride complexes IrXH(2)(eta(2)-H(2))(PR(3))(2) (X = Cl, Br, I) / S. Li, M. Hall, J. Eckert, C. Jensen, A. Albinati. - In: JOURNAL OF THE AMERICAN CHEMICAL SOCIETY. - ISSN 0002-7863. - 122:12(2000 Mar 29), pp. 2903-2910.

Transition metal polyhydride complexes. 10. Intramolecular hydrogen exchange in the octahedral iridium(III) dihydrogen dihydride complexes IrXH(2)(eta(2)-H(2))(PR(3))(2) (X = Cl, Br, I)

A. Albinati
Ultimo
2000-03-29

Abstract

Density functional calculations (B3LYP) on IrXH(2)(eta(2)-H(2))(PR(3))(2) for X = Cl, Br, I and R = H, Me and inelastic neutron scattering studies for X = Cl, Br, I and R = Pr(i) are used to elucidate the mechanisms for the intramolecular dihydrogen/hydride exchange. The two lowest energy processes are rotation of the dihydrogen ligand and oxidative addition of the dihydrogen to form an intermediate Ir(V) tetrahydride, which undergoes rapid reductive elimination to interchange the dihydrides and the dihydrogen. The use of PMe(3) as a model phosphine is essential to bring the calculated barriers for the dihydrogen/hydride interchange into agreement with the experimental observations. The activation energy for site exchange (1.9 kcal/mol) is found to be in excellent agreement with the experimental result obtained for X = Cl (1.5(2) kcal/mol), and the calculations show a slight decrease in this value from X = C1 to I. Comparison between calculated rotational barriers (0.3 to 0.7 kcal/mol) and experimental values obtained for IrXH(2)(eta(2)-H(2))(PR(3))(2) (X = Cl, Br, I; R = Pr(i)) (0.5 to 1.0 kcal/mol) also demonstrates that the quantitative estimate of the barrier to rotation requires PMe(3) as the minimal model ligand.
inelastic neutron-scattering; potential basis-sets; molecular-hydrogen; hydride ligands; polarization functions; solution equilibrium; perturbation-theory; coupled-cluster; hartree-fock; solid-state
Settore CHIM/03 - Chimica Generale e Inorganica
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/2434/256878
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