Ph.D., 2013, University of New South Wales
Research in the McSkimming group is focused on synthetic inorganic chemistry. Drawing inspiration from the active sites of metalloenzymes, our primary goal is to design and prepare precise ligand frameworks that support unusual and highly reactive metal complexes. Ultimately, we aim to develop creative and effective catalysts for the conversion of industrially important substrates such as CO and N2.
Inorganic chemistry, Organometallic chemistry
McSkimming, A.; Cheisson, T.; Carrol, P. J.; Schelter, E. J., Functional Synthetic Model for the Lanthanide-Dependent Quinoid Alcohol Dehydrogenase Active Site, J. Am. Chem. Soc., 2018, 140(4), 1223–1226.
McSkimming, A.; Harman, W. H., A Terminal N2 Complex of High-Spin Iron(I) in a Weak, Trigonal Ligand Field, J. Am. Chem. Soc., 2015, 137, 8940–8943.
McSkimming, A.; Bhadbhade, M. M.; Colbran, S. B., Bio‐Inspired Catalytic Imine Reduction by Rhodium Complexes with Tethered Hantzsch Pyridinium Groups: Evidence for Direct Hydride Transfer from Dihydropyridine to Metal‐Activated Substrate, Angew. Chem. Int. Ed. 2013, 52, 3411–3416.
McSkimming, A.; Colbran S. B., The coordination chemistry of organo-hydride donors: new prospects for efficient multi-electron reduction, Chem. Soc. Rev., 2013, 42, 5439–5488.
