Andryj Borys

@andryjborys.bsky.social

Assistant Editor at the Royal Society of Chemistry | Main-Group and Organometallic Chemist | Schlenk Line Enthusiast | #CASFutureLeaders '23

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I've got a fully funded PhD position in my group at Greenwich, doing some fun ligand design and main group (aluminium) catalysis with phosphazenes and ylids - please, share widely and drop me an email at e.clark@gre.ac.uk if you're interested. www.findaphd.com/phds/project...

Fully Funded Phosphazene Stabilised Ylids as Ligands for Aluminium Catalysis at University of Greenwich on FindAPhD.com

PhD Project - Fully Funded Phosphazene Stabilised Ylids as Ligands for Aluminium Catalysis at University of Greenwich, listed on FindAPhD.com

findaphd.com

Continuing our campaign to study all the alkali metals in organometallic chemistry. Why don't you try this in your own studies? Our friends in Bern @evaheviagroup.bsky.social are! Comparisons and Contrasts in a Complete Set of Alkali Metal Cumyl Structures | Inorg Chem pubs.acs.org/doi/10.1021/...

Comparisons and Contrasts in a Complete Set of Alkali Metal Cumyl Structures

Alkali-metal benzyl complexes derived from toluene are known to vary their metal–ligand coordination mode as a function of the alkali-metal, with the metal transitioning from a typical σ bond to the anionic CH2 for lithium toward an interaction with the delocalized pi system of the aromatic ring as the metal gets larger and softer. Here, by switching to cumene, we report the charge-localizing effect of replacing the hydrogen atoms at the formally carbanionic carbon CH2 with electron-donating methyl groups in C(Me)2. NMR spectroscopic studies reveal competitive ring-metalation occurs, at the meta and para positions, alongside α-metalation on using an alkyl lithium base, with the meta- and α-isomers crystallographically characterized as a solvated dimer and monomer, respectively. Using Lochmann-Schlosser type base pairs to access the heavier alkali-metal complexes unveils only α-metalation. The presence of the methyl groups limits the variation in metal–ligand bonding, their electron-donating properties forcing the delocalization of the negative charge into the ring resulting in M-Ph interactions and sp2 hybridization at the formally deprotonated α-carbon regardless of the metal used. Considerable variation in aggregation state is observed with monomeric (Na), polymeric (K, Cs) and tetrameric (Rb) motifs identified in the solid-state.

pubs.acs.org

Very proud of Luca and all his hard work on this challenging paper! I'll always remember my last few weeks in the @evaheviagroup.bsky.social which were spent preparing Li dendrites and Cs ampoules for this project!

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Eva Hevia@evaheviagroup.bsky.social · 8mo ago

Excited to share #LucaVedani and @andryjborys.bsky.social work on highly reduced #alkalimetal #nickelate complexes! A collaborative effort with #DietmarStalke to try to understand their structure and applications in #catalysis @pubs.acs.org #JACS @unibe.ch #TeamNi pubs.acs.org/doi/full/10....

🚨 PhD Opportunity 🚨 🔁 Reposts appreciated! My group at @manchester.ac.uk is recruiting a 3.5-year PhD student to explore Sb & Bi pincer complexes for metallomimetic chemistry. 🔬 Fully funded (UK only) 📍 Manchester 🧪 Synthetic inorganic chemistry Apply 👉 tinyurl.com/yrjkvha9

Sustainable Catalysis with Sb and Bi Pincer Complexes at The University of Manchester on FindAPhD.com

PhD Project - Sustainable Catalysis with Sb and Bi Pincer Complexes at The University of Manchester, listed on FindAPhD.com

tinyurl.com