There was a meme going around Twitter recently, based on sharing ‘cool chemistry’ – according to the writer’s own definition. The premise is that for each user who clicks the ‘like’ button on the original post, the writer will share one, sub-140-character snippet about something that is both cool and chemistry-related. It looks something like this:
But here is my contribution. Some of them are frivolous, some of them are complex, all of them are chemistry.
I did not completely stick to the rule of omitting context from the commentary:
(No offence to aluminium chemists.)
Check out p. S-3 of the Supporting Info here for one method of short-chain silica modification.
I expect this one is due to solvate isomerism:
Yes, I know this is a nickel paper. He’s versatile on transition metals (£):
Just to reiterate from Point 32, Amanda is a genius.
The link is to What’s Cooking in Chemistry?: How Leading Chemists Succeed in the Kitchen – a series of recipes prepared by well-known chemists.
Dodecahedrane synthesis is brilliantly summarized by BRSM.
Movassaghi and coworker’s report on Robinson’s synthesis, 96 years later (£).
Here’s a Noah Burns total synthesis paper proving that polychlorosulfolipids are, indeed, cool (£).
I’m referring to this conformational change.
Here’s a great paper from the Nakajima group of lithium acetylide addition to ketones and aldehydes in up to 98.5:1.5 er.
As retired chemist John Campbell pointed out, that is a typo for 15N labelling – 14N wouldn’t be much use!
18F is important as a positron source for PET scanning. It requires special modes of synthesis due to its short half life of 110 minutes.
This is actually the sulfate, but it’s visually similar:
With apologies to Nicki Minaj.
Betaine with his brother Ylid:
As always, e-EROS has a useful summary of nickel boride’s use as a reagent (£). If you can’t access that, Wikipedia offers a non-subscription alternative.
There were a lot more likes than I expected! Hope you learned something from the list. I found it instructive to write!