We present four proton-responsive palladium and platinum complexes, [MCl ( PONNHO)] (M=Pd, Pt; R= Pr, Bu) synthesised by complexation of PdCl or PtCl (COD) with the 1,8-naphthyridine ligand PONNHO. Deprotonation of [MCl ( PONNHO)] switches ligand coordination from mono- to dinucleating, offering a synthetic pathway to bimetallic Pd and Pt complexes [M Cl ( PONNO) ]. Two-electron reduction gives planar M -M complexes [M ( PONNO) ] (M=Pd, Pt) containing a metal-metal bond.
View Article and Find Full Text PDFMetal hydride complexes are essential intermediates in hydrogenation reactions. The hydride-donor ability determines the scope of use of these complexes. We present a new, simple mass-spectrometry method to study the hydride-donor ability of metal hydrides using a series of 18 iron, cobalt, and nickel complexes with and based ligands (L).
View Article and Find Full Text PDF