Organometallic chemistry combines the classical disciplines of Inorganic and Organic chemistry.
It deals with compounds in which a metal atom (half-metals and non-metals are included) is linked to a carbon atom of
an organic ligand. These products fullfill a variety of important functions as catalysts in modern industrial
processes, synthetic polymers with a large scope of applications, as precursors for high-tech materials and as
reagents in organic synthesis.
In our group the focus lies on the synthesis of new compounds where the aspects of basic and applied research
play an important role. The following topics are currently (2010) under investigation.
"Dynamic Covalent Chemistry" relates to chemical reactions carried out reversibly under conditions of equilibrium control.
In our group, this concept is applied in organogallium chemistry for the synthesis of compounds with novel structural features.
As an example, the reversible reactions of 1,1`-bis(dimethylgallyl)ferrocene to the two- and threefold 1,1´-ferrocenediyl
substituted gallium compounds are presented:
As part of the DFG-Research Group FOR 945 ("Nanomagnete: von der Synthese über die Wechselwirkung mit Oberflächen zur Funktion")
and in collaboration with the group of Prof. Dr. A. Hütten (Department of Physics) we investigate the synthesis and
characterization of ligand stabilized magnetic nanoparticles (Fe, Co, Fe/Co, Fe3O4) suitable for a further functionalization
with biomolecules [1] and of ligand stabilized core-shell particles (Co@Ru) suitable to study the GMR effect.
In the context with the experimental control of nanoparticle morphology, we are studying modifications of the
generally accepted "LaMer model" for the nucleation and growth step during particle formation from precursor
decomposition in solution, and we introduce the "droplet model".
The following topics are currently under research:
π-Complexation with cyclopentadienyl (Cp) ligands allows the isolation of sandwich- and half-sandwich
compounds with divalent silicon as central atom. Such complexes are regarded as the resting state of
highly reactive (η1-Cp)2Si-, (η1-Cp)RSi- and (η1-Cp)Si+ fragments, due to the electronic flexibility of the
respective Cp ligand (η2,3,5 - η1-rearrangment).
Actually, we investigate the chemistry of the (Me5C5)2Si and of
the Me5C5Si+ cation.
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