The intramolecular metalation of a β-silyl methyl group in [U{N(CH2CH2NSiMe2But)3}(CH2Ph)] occurs rapidly, despite the conformational demands of the triamidoamine ligand, to produce a highly strained metallacycle (U–C ca. 2.75 Å); this complex reacts cleanly with a range of carbon and other acids to give, for example, an alkynyl with a bent (156°) U–CC unit.
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Boaretto et al. (1999) studied this question.
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