Metal-Metal Redox Exchange to Produce Heterometallic Manga-nese-Cobalt Oxo Cubanes via a “Dangler” Intermediate

18 April 2024, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Pendent metals bound to heterocubanes are key components of well-known active sites in enzymes that mediate difficult chemical transformations. Investigations into the specific role of these metal ions, sometimes referred to as "danglers," have been hindered by a paucity of rational synthetic routes to appropriate model structures. To generate pendent metal ions bonded to an oxo cubane through a carboxylate bridge, the cubane Co4(μ3-O)4(OAc)4(t-Bupy)4 (OAc = acetate, t-Bupy = 4-tert-butylpyridine) was exposed to various metal acetate complexes. Reaction with Cu(OAc)2 gave the structur-ally characterized (by X-ray diffraction) dicopper dangler Cu2Co4(μ4-O)2(μ3-O)2(OAc)6(Cl)2(t-Bupy)4. In contrast, the anal-ogous reaction with Mn(OAc)2 produced the MnIV-containing cubane cation [MnCo3(μ3-O)4(OAc)4(t-Bupy)4]+ by way of a metal-metal exchange that gives Co(OAc)2 and [CoIII(μ-OH)(OAc)]n oligomers as byproducts. Additionally, reaction of the formally CoIV cubane complex [Co4(μ3-O)4(OAc)4(t-Bupy)4][PF6] with Mn(OAc)2 gave the corresponding Mn-containing cubane in 80% yield. A kinetic and mechanistic examination of the related metal-metal exchange reaction between Co4(μ3-O)4(OBz)4(py)4 (OBz = benzoate) and [Mn(acac)2(py)2][PF6] by UV-vis spectroscopy provided support for a pro-cess involving rate-determining association of the reactants and electron transfer through a μ-oxo bridge in the adduct intermediate. The rates of exchange correlate with the donor strength of the cubane pyridine and benzoate ligand sub-stituents; more electron-donating pyridine ligands accelerate metal-metal exchange, while both electron donating and withdrawing benzoate ligands can accelerate exchange. These experiments suggest that the basicity of the cubane oxo ligands promotes metal-metal exchange reactivity. The redox potentials of the Mn and cubane starting materials, and isotopic labeling studies, suggest an inner-sphere electron transfer mechanism in a dangler intermediate.

Supplementary materials

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Description
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Supporting Information
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Experimental procedures, characterization data, spectra, electrochemical characterization, and crystallographic tables.
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MnCo3 cif
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Crystallographic details for MnCo3
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Cu2Co4 cif
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Crystallographic details for Cu2Co4
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