Determination of the Temperature Dependence of the H--D Spin--Spin Coupling Constant and the Isotope Effect on the Proton Chemical Shift for the Compressed Dihydride Complex [Cp★Ir(P- P)H].

Complex [Cp*lr(dmpm)H] (dmpm = bis(dimethylphosphino)methane) has been reported to display temperature-dependent spin-spin coupling constant (1 ) and isotope effect on the H NMR chemical shift (Δ&delta). A combined electronic structure density functional theory + quantum nuclear dynamics study is us...

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Detalles Bibliográficos
Publicado en:	Journal of the American Chemical Society Vol. 127; no. 15; pp. 5632 - 5641
Autores principales:	Gelabert, Ricard, Moreno, Miquel, Liuch, José M., Liedos, Agusti, Heinekey, D. Michael
Formato:	Artículo
Publicado:	American Chemical Society 4/20/2005
Materias:	Particles (Nuclear physics) Electronic structure Density functionals Potential energy surfaces Quantum chemistry Line geometry
Acceso en línea:	Ver este registro en EBSCOhost

Descripción
Sumario:	Complex [Cp*lr(dmpm)H] (dmpm = bis(dimethylphosphino)methane) has been reported to display temperature-dependent spin-spin coupling constant (1 ) and isotope effect on the H NMR chemical shift (Δ&delta). A combined electronic structure density functional theory + quantum nuclear dynamics study is used to determine from first-principles the unusual temperature dependence of the spin-spin coupling constant. It is found that the potential energy surface describing the motion of the lr-H2 unit has a deeper minimum in the dihydride region and is characterized by important anharmonicities. These anomalies affect the nature of the vibrational states of the unit and are the main reason for the unusual temperature dependence of 1 and Δ&delta. These results suggest experimental tests to identify compressed dihydride transition metal complexes.