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Veni grant for Dr Edwin Otten

31 July 2011

The Netherlands Organisation for Scientific Research has awarded Dr Edwin Otten of the Stratingh Institute for Chemistry a EUR 250,000 Veni grant within the framework of the Innovational Research Incentives Scheme. Veni grants are intended for young researchers who have recently gained a PhD and have significant and original talent for innovative research. Otten’s research is entitled ‘Direct Activation of Oxygen by Early Transition Metal Complexes: From Fundamental Science to Application in Oxidation Catalysis’.

Veni grants give young researchers a financial incentive (up to a maximum of EUR 250,000) for a period of three years to further develop their ideas. In addition to the Veni grant, the Innovational Research Incentives Scheme includes two other grant types as well: Vidi grants for experienced postdocs and Vici grants for senior researchers, both of which are also awarded annually.


Direct Activation of Oxygen by Early Transition Metal Complexes: From Fundamental Science to Application in Oxidation Catalysis’

The direct use of dioxygen (O2) in catalytic oxidation processes is a major challenge and is of substantial economic importance in bulk and fine chemical production, e.g. adipic acid. I propose to develop a new class of compounds that will activate dioxygen and mediate O-transfer to (organic) substrates. The compounds to be studied will be based on early transition metals, which normally do not interact readily with O2 in a controllable fashion. The fundamental problem is the strong tendency for early transition metals to form complexes in high oxidation states that lack the electrons required for O2 activation. The approach taken in this project will utilize redox-active ligands to overcome this problem. Redox-active ligands can facilitate unusual oxidation/reduction events at metal centers that are otherwise reluctant to participate in redox reactions. The interaction between early transition metal complexes bearing new redox-active ligands and dioxygen is largely unexplored. This project will focus on the chemistry of formally low-valent early transition metal complexes in which the metal d-electrons are (partially) delocalized into the ligand framework. These electrons are available for interaction with dioxygen, which will allow for its activation to give metal-peroxo species. The subsequent selective O-atom transfer to (organic) substrates will be investigated and form the basis for the development of a new paradigm in oxidation catalysis, in which dioxygen is the terminal oxidant.

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Dr. E. Otten, Molecular Inorganic Chemistry, Strating Institute for Chemistry

Last modified:10 February 2017 3.10 p.m.
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