Prof. Dr. John F. Hartwig
The first awardee in 2011 is the American chemist Prof. John F. Hartwig. He made his debut as recipient of the Einstein Foundation Award in the German Cluster of Excellence “Unifying Concepts in Catalysis” (UniCat) on 29th June 2011. Following the official presentation of his letter of appointment as “Einstein Visiting Fellow”, he gave his inaugural lecture on the site-selective functionalization of carbon-hydrogen bonds for the more efficient use of hydrocarbons in the supply chain.
“John Hartwig is a major star in the organometallic catalysis field. His creative approaches will generate new, unforeseen interdisciplinary synergies in our Cluster of Excellence. It feels like we are a Premier League football team when a new top player joins the team,” enthuses Prof. Matthias Driess, chair of UniCat, who is very pleased with this boost to the homogeneous catalysis field.
The scientist is to visit Berlin several times a year, where he initiates research projects with his Berlin colleagues and spends some time teaching. The Einstein Foundation Berlin provides €150,000 per fellow per year, which affords the means to set up a Berlin working group.
First Einstein Awardee: John Hartwig
John Hartwig (46) has written over 250 publications and is one of the 50 most-quoted chemists in any area of study. Until recently he was Professor of Chemistry at the University of Illinois, USA, changing a few weeks ago to the renowned University of California, Berkeley. Even at the very start of his scientific career he was already making a series of spectacular discoveries thanks to which the catalytic transformation of hydrocarbons into functionalized reusable materials was possible for the first time.
|1540 Iridium-Catalyzed Regioselective Silylation of Aromatic and Benzylic CH Bonds Directed by a Secondary Amine Q. Li, M. Driess, J. F. Hartwig Angewandte Chemie International Edition 2014, 32, 8471–8474, 10.1002/anie.201404620 |
|1536 Iridium-Catalyzed Regioselective Silylation of Secondary Alkyl C–H Bonds for the Synthesis of 1,3-Diols B. Li, M. Driess, J. F. Hartwig Journal of the American Chemical Society 2014, 18, 6586–6589, 10.1021/ja5026479 |
|1533 Copper-Catalyzed Oxidative Dehydrogenative Carboxylation of Unactivated Alkanes to Allylic Esters via Alkenes B. L. Tran, M. Driess, J. F. Hartwig Journal of the American Chemical Society 2014, 49, 17292–17301, 10.1021/ja510093x |
|1386 Copper-Catalyzed Intermolecular Amidation and Imidation of Unactivated Alkanes B. L. Tran, B. Li, M. Driess, J. F. Hartwig Journal of the American Chemical Society 2014, 6, 2555–2563, 10.1021/ja411912p |
|1288 From Bis(silylene) and Bis(germylene) Pincer-Type Nickel(II) Complexes to Isolable Intermediates of the Nickel-Catalyzed Sonogashira Cross-Coupling Reaction D. Gallego, A. Brück, E. Irran, F. Meier, M. Kaupp, M. Driess, J. F. Hartwig Journal of the American Chemical Society 2013, 41, 15617–15626, 10.1021/ja408137t |
|986 Pushing the σ-Donor Strength in Iridium Pincer Complexes: Bis(silylene) and Bis(germylene) Ligands Are Stronger Donors than Bis(phosphorus(III)) Ligands A. Brück, D. Gallego, W. Wang, E. Irran, M. Driess, J. F. Hartwig Angewandte Chemie International Edition 2012, 46, 11478–11482, 10.1002/anie.201205570 |