this post was submitted on 20 Oct 2024
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is that even stable? been too long since organic chemistry class
Dicarbon monoxide. Wikipedia is shockingly poor in information about it, but "stable" is certainly not the first word I'd use to describe it.
You could also do something like a cross between https://en.m.wikipedia.org/wiki/Ethylene_oxide and https://en.m.wikipedia.org/wiki/Acetylene (the fuel responsible for the hottest welding flames) but remove the hydrogens and then have the carbons do a triple bond to make https://pubchem.ncbi.nlm.nih.gov/compound/Epoxy-acetylene
Considering ethylene oxide is already so unstable as fuck though due to its strained structure that it's used as the main component in thermobaric weapons and this would be even more strained with a very unstable triple carbon bond, I don't know if that would be an improvement. This ring would also likely cause mega cancer when it's not exploding, pretty much all the https://en.m.wikipedia.org/wiki/Epoxide rings cause cancer and this one is particularly unstable (though I don't really know if this one would because its not an alkening agent, which is why the other ones are so hostile, this one would be so reactive that it likely would immediately create some cancer causing compounds as soon as it met biological tissue).
Not that I know that is really possible to make. Chatgpt hallucinates a pathway and I never took organic chemistry so I can't really criticize it. Google doesn't really present with any answers. I'd imagine you'd need very low temperatures and an esoteric pathway.