Research Interests
Research in the Neidig group spans synthetic and mechanistic organometallic chemistry, catalysis and physical-inorganic chemistry. One major area of interest focuses on elucidating active catalyst structure and mechanism in Earth-abundant metal catalysed transformations for organic synthesis to foster and facilitate sustainable catalyst and methodology development. Additional areas of interest include synthetic, spectroscopic and reactivity studies in molecular f-element chemistry as well as spectroscopic and electronic structure studies in support of broader research efforts across a range of inorganic, bioinorganic and materials chemistry systems. Some examples of specific areas of research interest are given below.

Iron-Catalysed Transformations for Sustainable Catalysis in Organic Synthesis and Beyond
A major research focus of the Neidig group is the development of fundamental knowledge of active catalyst structure and mechanism in earth abundant metal catalysis in order to foster and facilitate new catalyst and methodology development. Of particular interest are iron-catalysed transformations which offer tremendous potential for sustainable, low-cost methodologies for the selective formation of C-C, C-N and other carbon-heteroatom bonds. Unfortunately, a detailed understanding of in situ speciation and mechanism in such iron-catalysed transformations has remained largely elusive, reflecting both the broad range of plausible reaction mechanisms for paramagnetic iron complexes in catalysis (including both one and two electron pathways) and the experimental challenges associated with characterizing paramagnetic iron complexes. These challenges have historically presented a barrier to understanding the basic science that governs iron catalysed processes in organic chemistry, generally precluding the rational, mechanistic driven catalyst development that has proven widely successful in palladium chemistry. To address this significant limitation, our group has pioneered a distinct technical approach for studies of open-shell iron catalysts in organic transformations, utilizing a combination of inert atmosphere synthesis, advanced inorganic spectroscopic methods (e.g. Mössbauer spectroscopy, EPR, etc.) and DFT methods in order to obtain detailed information on the electronic structure of iron catalysts involved in organic transformations, including molecular-level insight into in situ generated and transient iron species. In parallel, we utilize this insight for new ligand and reaction development in iron catalysis. Example reactions of interest include iron-catalysed cross-couplings, C-H activation/functionalisations and olefin functionalisations, amongst others.