Research

Page

Overview

Our lab investigates the effect coordination environment has on the reduction and oxidation properties of transition metals. This research has applications in the field of organometallic chemistry for the rational synthesis of transition-metal catalysts that perform desired chemical reactions.

The synthesis, structure and coordination chemistry of chelating ligands bearing sulfur-containing pendant groups.

We are currently interested in synthesizing new ligands with sulfur-containing pendant groups and investigating the structures that can be formed upon coordination to transition metals. Phosphadiazanes are a class of bidentate ligands that provide two phosphorus donors to a transition metal. Phosphadizanes are generated by the reaction between a primary amine and a phosphine chloride. By altering the identity of either component, a variety of ligands can be synthesized bearing varying steric and electronic properties. Recently, we have been using novel Schiff-base ligands derived from salicylaldehyde bearing a mercaptoimidazole pendant group (Below, Right). X-ray diffraction data has allowed us to investigate the coordination chemistry of these new ligands with a variety of transition metals. The hope is that these ligands can be used as scaffolds for interesting 2D and 3D structures in the solid-state.