Density functional theory study of the d(10) series (H3P)3M(eta 1-SO2) and (MenPh(3-n)P)3M(eta 1-SO2) (M = Ni, Pd, Pt; n = 0-3): SO2 pyramidality and M-S bond dissociation energies.

Abstract

Quantum mechanical density functional theory (DFT) and coupled DFT/molecular mechanics (QMMM) studies of the compounds (H(3)P)(3)M(eta(1)-SO(2)) and (Me(n)Ph(3-n)P)(3)M(eta(1)-SO(2)) (M = Ni, Pd, Pt; n = 0-3) model the experimental data well, particularly the planar/pyramidal geometries at sulfur. Bond dissociation energy (BDE) calculations confirm that Pd/Pt systems with pyramidal SO(2) ligands exhibit M-S BDEs smaller by 30-50% than Ni systems with planar SO(2). However, scans of the potential energy surfaces show that flexing the planar/pyramidal torsion angle within ranges of 20-30 degrees requires little energy. Bond energy decomposition calculations indicate that the electrostatic Delta E(elstat) term determines the BDE for Pd/Pt molecules where the sulfur is pyramidal, whereas all three terms matter when the sulfur is planar, as for Ni compounds. However, this accounts only for a fraction of the BDE differences; orbital energy matching accounts for the balance.