P is a Lewis base, a Lewis acid, a transition metal, it’s red, it’s white, it’s the rainbow, call it a chameleon at this point. Beautiful work !!

I'm hopping back onto Xwitter real quick to share that we've published our paper on using Mie Resonant metal oxide catalytic supports to produce broadband rate enhancements for photocatalysis! Optical synergies lead to improved performance. pubs.acs.org/doi/10.1021/ac…

Ok delta 😂🫠

We're hiring! Together with Prof. Marcus Drover we are looking for a motivated candidate ready to embark on a 3-y doctorate between France and Canada. Topic: molecular hybrid metal/main group donor-acceptor systems for small molecule activation.

The Carsch Group at UT Austin is actively recruiting new postdoctoral researcher(s) for this winter! Applicants should send an email to [email protected] with a cover letter on research interests, a detailed CV, and statement of prior work.

🧪 Calling Exceptional Chemists! 🔬 Join our vibrant Process Chemistry team in Rahway, NJ. Drive innovative solutions for complex challenges - from drug candidate manufacturing routes to pioneering new methodologies.💫 #Merck #InventingForLife #Chemjobs jobs.merck.com/us/en/job/R310…

Excited to present the first paper from the Park group, published today in Science Magazine! We found a user-friendly, mild reaction conditions for exchanging an oxygen in heterocycles with nitrogen groups. Congrats Donghyeon, Jaehyun, and the team! science.org/doi/10.1126/sc…

Our first publication (!) detailing important advantages of voltage-controlled electrolysis through the development of a Shono-type amination reaction has now been published J. Am. Chem. Soc.! Congrats to Siyuan and the team 🥳 #chemtwitter pubs.acs.org/doi/10.1021/ja…

Our latest dinickel catalysis paper is out now in JACS ASAP! See Chris, Chengyi, and Perry’s work on hindered azoarene synthesis through N=N coupling below 🧪 pubs.acs.org/doi/10.1021/ja…

Fall vibes in all labs 👀

Our latest now on ChemRxiv – @aidanlooby28, Lalu, and Wenjun developed a slick entry to oxidative addition complexes that bypasses typical need for independent synthesis with every ligand iteration chemrxiv.org/engage/chemrxi…

Did you catch this months episode? We go with the FLOW with Kyle and Mike to talk about flow solid phase peptide synthesis. #MerckChemistry podcasts.apple.com/us/podcast/pha…

Electrifying synthetic community without electrifying a radical precursor

Finally, a radical–radical cross-coupling! After 180 years of generating C-radicals from carboxylic acids, we can now couple them with radicals from organoboron reagents. In our first ChemRxiv we introduce redox matched electrolysis to discover a “carboxylic acid–organoboron

Congrats Arnaud, Laboratoire LBPB, Bourissou , Rinoi ghenwa Bouhadir , Laboratoire Hétérochimie Fondamentale et Appliquée !! Really cool compounds :)

SNAr powers the engine of drug discovery and production, but electronic demands restrict access to important chemical space. We describe an e-SNAr strategy to bridge this gap that operates under air at RT with catalytic charge, simplifying scalability. chemrxiv.org/engage/chemrxi…

Check out our most recent publication in J. Am. Chem. Soc. 💥 "Planarity Is Not Plain: Closed- vs Open-Shell Reactivity of a Structurally Constrained, Doubly Reduced Arylborane toward Fluorobenzenes" pubs.acs.org/doi/10.1021/ja… Congrats! 🎊 Christoph Buch Felipe Fantuzzi

Another Organometallics Flash Communication! From Chirik Group's Cherish Nie on Ni-promoted ring opening of vinylcyclobutanes. pubs.acs.org/doi/10.1021/ac…