Coulombic inter-ligand repulsion effects on the Pt(ii) coordination chemistry of oligocationic, ammonium-functionalized triarylphosphines

Abstract

The Pt(II) coordination chemistry of oligocationic ammoniomethyl- and neutral aminomethyl-substituted triarylphosphines (L) is described. Complexes of the type PtX(2)(L)(2) (X = Cl, I) have been isolated and characterized. For the hexa-meta-ammoniomethyl-substituted ligands [1](6+) and [2](6+), two ligands always occupy a trans-configuration with respect to each other in complexes of the type PtX(2)(L)(2), while for the tri-para-ammoniomethyl-substituted ligand [7](3+), the trans/cis ratio is dependent on the ionic strength of the solution. This behaviour was not observed for the neutral aminomethyl-substituted ligands. In the crystal structure of trans-[PtI(2)(1)(2)]I(12), the geometrical parameters of the phosphine ligand [1](6+) are very similar to those found in the analogous complex of the benchmark ligand PPh(3), i.e. trans-PtI(2)(PPh(3))(2), indicating that no significant increase in the steric congestion is present in the complex. Instead, the coordination chemistry of this class of phosphine ligands is dominated by repulsive Coulombic inter-ligand interactions.