This idea was especially inspired by the really cool work on halogen transfer done by fellow @CSBSJU alumnus Jeff Bandar, who’s research I’ve always thought was really exciting and creative! I was hyped to apply that work in the continuing Roberts group arynes lineage.
Really hyped to share my latest work in grad school focusing on a fun difunctionalization of arynes! @robertsgroupumn we show halogen transfer can install halogens competitive to protons! Thanks to the team @CortnieRoberts and our awesome undergrad Lars!
https://t.co/8cCewPDocj
@NMRspectroscopy Legitimate question: don’t atoms in identical environments not couple with each other? Those fluorine atoms look identical by a symmetry plane parallel to the arene, so I wouldn’t have thought they would couple with each other.
I found out the other day that there are multiple ways people pronounce “ORCID” and 1) I am shook, but 2) what does #ChemTwitter do?? Asking for science.
(Thread) In the first What If? book, I answered a question about cooking a steak by dropping it from space. At one point, I commented—jokingly!—that if anyone put a steak in a hypersonic wind tunnel to gather better data, I’d love to see the video.
Well, I have good news.
@hotbrother3 Kügelrohr was not something that came to mind but is worth trying!
I like the other suggestions too, I hadn’t thought of it in the frame of removing product instead. Some products might be trace, but I’ll explore that all the same. Thanks!
Q for #ChemTwitter, any magic advice out there on removing PhCN from a reaction? Trying to see if it’s my magic solvent, and it’s not making it easy. Maybe the DMF tricks with LiCl or #TeamHeptane azeotrope can help? #RealTimeChem
@ndchiappini That CCHF seminar from Du Bois was actually what inspired me to try PhCN and tBuCN in the first place!
tBuCN has solubility issues with some reaction components, although I plan to try optimizing those so maybe it’ll improve. Otherwise, xylenes azeotrope? I’ll give it a go 😅