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Dynamic Processes of H-Atom Site Exchange In Trans Dihydrogen Hydride Complex of Ruthenium

Sivakumar, V and Jagirdar, Balaji R (2005) Dynamic Processes of H-Atom Site Exchange In Trans Dihydrogen Hydride Complex of Ruthenium. In: Indian Journal of Chemistry Section A- Inorganic Bio-Inorganic Physical, 44 (1). pp. 27-33.

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Official URL: http://cat.inist.fr/?aModele=afficheN&cpsidt=16408...

Abstract

A new dihydrogen hydride complex of ruthenium of the type trans-$[(dppm)Ru(H)(h^2-H_2)(PPh_3)_2][BF_4] (l) (dppm = Ph_2PCH_2PPh_2)$ has been prepared by protonating the precursor dihydride complex cis-$[(dppm)Ru(H)_2(PPh_3)_2]$ using $HBF_4.Et2O$. The formulation of (l) as a dihydrogen complex has been based upon the variable temperature $T_1$ measurements $(T_1(min) = 12.4 ms at 273 K, ClCD_2CD_2Cl, 400 MHz)$ and the observation of a substantial H-D coupling constant $(J(H,D) = 32 Hz, 243 K, ClCD_2CD_2Cl)$ for the corresponding HD isotopomer trans-$[(dppm)Ru(H)(h^2-HD)(PPh_3)_2][BF_4]$. The T1 and the H-D coupling constant measurements have been carried out in the temperature range 243 – 283 K. The dihydrogen and the hydride ligands of (l) show dynamic behavior and undergo rapid H-atom site exchange at 343 K. At 273 K (l) shows a static structure. The dynamics of (l) involving a trihydride intermediate has been studied by variable temperature NMR spectroscopy. The barrier to site exchange of the H-atom between the dihydrogen with the hydride (DG‡) has been determined to be 14.4 kcal/mol at 303 K. Compound (l) has been found to be stable up to 343 K in solution and no loss of the $H_2$ ligand has been observed at that temperature; in addition, the compound is stable in solution at room temperature for a period of two days.

Item Type: Journal Article
Additional Information: The copyright for this article belongs to National Institite for Science Communication.
Department/Centre: Division of Chemical Sciences > Inorganic & Physical Chemistry
Date Deposited: 01 Mar 2005
Last Modified: 20 Jan 2012 05:58
URI: http://eprints.iisc.ernet.in/id/eprint/2834

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