coburgerpeter.bsky.social

@coburgerpeter.bsky.social

https://www.coburger-lab.de We are a research group @ TUM, focussing on the reactivity of biradicaloid complexes.

Christian's in depth study on small molecule diffusion theory for DOSY NMR analysis is out now in Chem. Eur. J.: doi.org/10.1002/chem.... He developed a new semi-empirical model based on the molecular volume which describes diffusion of molecules and complexes with the lowest error so far. #chemsky

Accurate Molecular Size Determination by Diffusion Ordered NMR Spectroscopy Based on an Improved Diffusion Model

A semi-empirical Stokes-Einstein-based model for describing the diffusion of organic, organometallic and coordination compounds is developed for the interpretation of diffusion constants obtained by ....

doi.org

They did it! @rsc.org has successfully “optimized” their journal websites to a new and improved 1998 state - extra clicks, slow server response, and TOC figures hidden so deeply in the weeds that it’s impossible to scan the latest papers. It feels like no scientists were involved in the process…

I’m delighted to share that I have been awarded the Sir Edward Frankland Prize by the Royal Society of Chemistry. This recognition reflects the awesome work of my research group members, whose dedication and creativity make everything possible. www.rsc.org/standards-an...

Dr Josh Abbenseth

For advancing the chemistry of geometrically constrained heavy pnictogen pincer compounds to access exotic radical states and unique transition metal mimetic reaction pathways.

rsc.org

New paper online 🥳 In Franka‘s 2nd paper she successfully synthesized 2 new isolable phosphonioacetylides 🤩 Check out pubs.acs.org/doi/10.1021/... for more details on the design principles and the resulting properties! Special thanks to @caputogroup.bsky.social for their supporting contribution 🤝

Isolable Phosphonioacetylides as Strong Neutral Carbon Donors with Variable Steric Demand and Tunable Donor Properties

Phosphonioacetylides are rod-shaped, neutral carbon donors with ambiphilic character at the terminal carbon. Despite their analogy to CO and isocyanides, they remain underexplored due to their high reactivity, and only one isolable free phosphonioacetylide has been reported. Here, we describe two new isolable, room-temperature-persistent examples stabilized either by two N-heterocyclic imines (NHIs) bearing bulky, flexible tert-octyl groups or by a single dipp-substituted NHI combined with alkyl substituents. Comprehensive characterization (SCXRD, NMR, IR, MS, DFT) confirms their strong donor properties and the accessibility of the reactive C2 unit. DFT analysis quantify how the substituents at phosphorus modulate the frontier molecular orbital energies, spanning a wide range of σ and π-donor strengths and π-acceptor abilities, with trends that mirror those of the corresponding phosphines. Both phosphonioacetylides readily form AuI complexes, whereas the less electron-rich compound shows the tendency to eliminate its C2 moiety thermally or upon hydrolysis. These results establish design principles for stabilizing and tuning phosphonioacetylides and open avenues for their use in coordination chemistry and catalysis.

pubs.acs.org

Nice to see our latest work in the ChemistryViews news section - thanks for the coverage! Check it out, if you wanna know more about our approach of stabilising unusual P-heterocycles in the coordination sphere of transition metals! www.chemistryviews.org/building-sta...

Building Stable Phosphorus Ligands - ChemistryViews

Researchers embed unstable phosphorus ligands directly in manganese and cobalt complexes, creating strong π‑donors with tunable reactivity

chemistryviews.org

💬🧪 Behind the Science Interview: P. Coburger & S. Frei discuss a method to build highly tunable strongly π-donating zwitterionic diphosphacyclobutadienyl ligands directly in Mn & Co complexes-enabling exploration of transitionmetal chemistry without isolating unstable ligands doi.org/10.1002/chem...

Building Zwitterionic Phosphorus Analogues of Cyclobutadienyl Ligands within the Metal Coordination Sphere - ChemistryViews

Peter Coburger and Stefan Frei, Germany, discusses assembling highly tunable, strongly π-donating zwitterionic diphosphacyclobutadienyl ligands directly within Mn and Co complexes

doi.org

Five years in the making, now finally published: Targeted synthesis of an inorganic sandwich complex. Congratulations to all co-authors and thanks to our collaborators: Eduardo García Padilla, Kai Schwedtmann, Demi Snabilie, Prof. Dr. Jan J. Weigand and Bas de Bruin! tinyurl.com/2v3xnwby

Inorganic Cobalt Sandwich Complex [(η5-P5)Co(η3-P3)]−

Sandwich compounds are foundational to organometallic chemistry, yet carbon-free analogs remain exceptionally rare. We report the all-phosphorus heteroleptic cobalt sandwich anion [(η5-P5)Co(η3-P3)]− ...

pubs.acs.org

Our 1st paper of '26 is out in @chemicalscience.rsc.org, led by PhD student Jonas 🥳 BIG congrats on your 1st paper! We find new cooperative OA/RE mechanisms at the Sn-Ni interface. This opens new perspectives in multi-metallic catalysis, coming soon..🧪 Also, cool compounds 🔥 tinyurl.com/2kx5z6pc

Cooperative metathesis of H–H/Sn–CAr bonds in stannylene-Ni0 systems

The reaction of phosphine-appended (amido)(aryl)stannylenes (1) with Ni0 synthons leads to the facile formation of chelating-stannylene Ni0 complexes (2–4). Utilising the carbene-stabilised synthon IP...

tinyurl.com