Different reaction products as a function of solvent: NMR spectroscopic and crystallographic characterization of the products of the reaction of gold(III) with 2-(aminomethyl)pyridine

Abstract

© 2015 Elsevier Ltd. All rights reserved. The reaction between equimolar amounts of hydrogen tetrachloridoaurate(III) trihydrate (H[AuCl4]·3H2O) and 2-(aminomethyl)pyridine (AMP) has been investigated under different reaction conditions. When these reactants were mixed in ethanol with an equimolar amount of HCl and at room temperature, the reaction yielded a gold(III) complex having bidentate coordinated AMP ligand, [Au(AMP)Cl2]Cl·H2O (1). However, in the aqueous solution of HCl (pH ≤ 1.00) at 50 °C no coordination of AMP ligand to Au(III) ion was observed and only H2AMP2+Cl-[AuCl4]-·0.5H2O (2) was obtained as the final product. While chelation by AMP ligand in ethanol has stabilized the Au(III) oxidation state, dominant reaction process occurring in water solvent at pH range 1.00-5.00 was reduction of Au(III) to the elemental gold, Au(0), which was rapidly accelerated by increasing pH. Both products 1 and 2 have been characterized by NMR spectroscopic and X-ray diffraction techniques. In crystals, the square-planar coordination around the Au(III) centers is supplemented to elongated square pyramidal (1) or octahedral (2) by means of Au...Cl interactions. This is achieved by either arranging the neighboring Au-Cl dipoles in antiparallel (1) or herring-bone (2) mode and additionally engaging in these interactions of the uncoordinated chloride ion (2).