A simple coordination complex of uranium(III), a uranium tris(amide), can selectively couple gaseous CO to the linear ynediolate [OCCO]2− dianion, at room temperature and pressure, regardless of the reagent stoichiometry. This product exhibits further reactivity upon warming in the form of the addition of a C–H bond of a methyl group across the CC triple bond, this second carbon–carbon bond forming reaction generating a functionalised enediolate dianion.
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Arnold et al. (2010) studied this question.
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