We focus on the coordination chemistry of unusual cyclic phosphorus-centered biradicaloids. Despite their exotic nature, these biradicaloids have some very appealing properties for the development of functional and cooperative ligands such as their strong binding to metal centers, their redox non-innocent behavior and the presence of Lewis-basic sites.
Our goal is to use these properties to develop more sustainable approaches in homogeneous catalysis, specifically by using biradicaloid ligands to enable first-row transition metals and main-group metals to mimic the behavior of noble metals in olefin functionalization.
Shown on the right below are two typical biradicaloids and representative complexes thereof which are used in our group:


Chemical laboratories have a significant carbon footprint. To tackle the climate crisis effectively, it is essential to conduct relevant research activities while ensuring they are carried out sustainably. By implementing sustainable practices, scientists can set an example and inspire positive change within the wider community. For more information, you can find an article detailing the principles of sustainable laboratory practices here.
In our own laboratoy, we try to implement as much of these concepts as possible. In particular, we aim to:
In the future, we also aim to use more ressource-friendly benchtop analytical devices (NMR, EPR etc.) for routine measurements.

A modular synthetic approach affords a series of cationic cobalt and manganese carbonyl half-sandwich complexes bearing onium-substituted diphosphacyclobutadienyl ligands. In this strategy, the onium substituents are readily varied, and the cyclobutadienyl ligand is assembled in situ within the metal coordination sphere. The resulting complexes provide a platform to systematically study the properties and reactivity of these unique ligands.

A series of cationic main-group complexes was obtained using the neutral, zwitterionic ligand IDP. The Lewis acidity of these complexes is explored by catalytic hydrophosphinations and halide addition reactions. The latter allow for the isolation of unusual π-complexes of tetryliumylidenes.

Reduction and oxidation of a phosphacyclic biradicaloid leads to reactive radical species which undergo selective dimerisation reactions.

A computational inspection of the bonding in clusters [Pn(Au·PMe3)4]+ (Pn = N–As) is presented. This ultimately finds that aurophilic interactions play a significant role in the switch from a tetrahedral to a square-pyramidal geometry for P and As, the closer Au···Au contacts in this conformer amounting to ≈15 kcal mol−1 stabilization energy, overcoming strong P/As3−–[Au4]4+ electrostatic interactions for the hypothetical tetrahedral form.

The synthesis of a phosphonium-substituted diphosphaindenylide, PPI, is reported. Introduction of two P atoms to the indenyl core results in considerable biradical character. Moreover, the ligand properties of PPI are investigated using a chromium tricarbonyl complex as model compound.

The reaction mechanisms for the reduction induced rearrangement of a series of pyramidanes into their cyclopentadienide derivatives were elucidated using density functional calculations. The calculations indicate that the reductions might proceed in a facile manner. However, the re-oxidation of the cyclopentadienide might yield meta-stable cyclic species. The latter represent intriguing synthetic targets.














Peter received his Master's degree from the University of Leipzig in 2015. He then conducted his PhD research with Prof. Evamarie Hey-Hawkins (2015 - 2019, University of Leipzig). The research focussed on utilizing carborane-substituted diphosphetanes as synthons for new phosphorus-based ligands. The PhD project was followed by a postdoctoral research project with Prof. Robert Wolf (2019 - 2020, University of Regensburg). This focussed on the computational exploration of unusual phosphorus ligands and their metal complexes. Then, following his passion for exotic phosphorus compounds, Peter relocated to the ETH Zurich to work as a postdoctoral research fellow in the group of Prof. Hansjörg Grützmacher (2020 - 2022). Here, he developed the coordination chemistry and redox chemistry of biradicaloid ligands. At the beginning of 2023, he started his independent research career at the TU Munich, initially supported by a Liebig Fellowship of the FCI and from 2024 onwards funded by the Emmy-Noether programme of the DFG.