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Cage Rearrangements in Dodecanuclear Co–Pt Dicarbido Clusters Promoted by Redox Reactions

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Abstract

The chemical reduction of [Co8Pt4C2(CO)24]2– ([1]2–) with Na/naphthalene results, after workup, in the isolation of either [Co10Pt2C2(CO)22]4– ([2]4–) or [Co8Pt4C2(CO)20]4– ([3]4–), depending on the experimental conditions. All these species undergo several chemical and/or electrochemical redox reactions, disclosing the existence of structurally related dodecanuclear clusters [1]n (n = 0–4), [2]n (n = 2–6) and [3]n(n = 1–7). In the attempt to isolate more reduced species,[1]n, [2]n and [3]n undergo structural rearrangements resulting, among others, in the formation of the new species [Co10–xPt2+xC2(CO)24]2– ([4]2–) (x = 0–2) structurally related to [1]2–. These dodecanuclear M12C2 dicarbido clusters are not isostructural and differ in the metal composition and/or the number of CO ligands. Nevertheless, they can be readily interconverted even if the interconversion reactions are not straightforward.

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