Density functional theory study on structural isomers and bonding of model complexes M(CO)5(BH3·PH3) (M = Cr, Mo, W) and W(CO)5(BH3·AH3) (A = N, P, As, Sb)

Ariafard, AlirezaAmini, Mostafa M.Azadmehr, Amirreza2026-01-012026-01-010022-328XORCID:/0000-0003-2383-6380/work/163628706https://hdl.handle.net/1885/733800797The influence of group 15 various substituents and effect of metal centers on metal-borane interactions and structural isomers of transition metal-borane complexes W(CO)5(BH3·AH3) and M(CO) 5(BH3·PH3) (A = N, P, As, and Sb; M = Cr, Mo, and W), were investigated by pure density functional theory at BP86 level. The following results were observed: (a) the ground state is monodentate, η1, with C1 point group; (b) in all complexes, the η1 isomer with CS symmetry on potential energy surface is the transition state for oscillating borane; (c) the η2 isomer is the transition state for the hydrogens interchange mechanism; (d) in W(CO)5(BH3·AH3), the degree of pyramidalization at boron, interaction energy as well as charge transfer between metal and boron moieties, energy barrier for interchanging hydrogens, and diffuseness of A increase along the series A = Sb < As Cr > Mo, while energy barrier for interchanging hydrogens decreases in the order of M = Cr > W > Mo.10enBorane complexesCharge transferDensity functional calculationsDensity functional theory study on structural isomers and bonding of model complexes M(CO)5(BH3·PH3) (M = Cr, Mo, W) and W(CO)5(BH3·AH3) (A = N, P, As, Sb)2005-03-0110.1016/j.jorganchem.2004.11.02114144252349