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Structure and Reactivity of One- and Two-Electron Oxidized Manganese(V) Nitrido Complexes Bearing a Bulky Corrole Ligand. | LitMetric

AI Article Synopsis

  • Researchers have developed a stable yet highly reactive manganese(V) nitrido complex using a bulky corrole ligand, showing promising properties for N atom transfer reactions.
  • The synthesized manganese complexes can be oxidized to form neutral and cationic variants, which have been structurally analyzed using X-ray crystallography.
  • The key manganese(V) nitrido complex exhibits exceptional reactivity in N atom transfer reactions, significantly outpacing the reactivity of previously known nitrido complexes.

Article Abstract

As a strategy to design stable but highly reactive metal nitrido species, we have synthesized a manganese(V) nitrido complex bearing a bulky corrole ligand, [Mn(N)(TTPPC)] (, TTPPC is the trianion of 5,10,15-Tris(2,4,6-triphenylphenyl)corrole). Complex is readily oxidized by 1 equiv of CpFe to give the neutral complex , which can be further oxidized by 1 equiv of [(-Br-CH)N][B(CF)] to afford the cationic complex . All three complexes are stable in the solid state and in CHCl solution, and their molecular structures have been determined by X-ray crystallography. Spectroscopic and theoretical studies indicate that complexes and are best formulated as Mn(V) nitrido π-cation corrole [Mn(N)(TTPPC)] and Mn(V) nitrido π-dication corrole [Mn(N)(TTPPC)], respectively. Complex is the most reactive N atom transfer reagent among isolated nitrido complexes; it reacts with PPh and styrene with second-order rate constants of 2.12 × 10 and 1.95 × 10 M s, respectively, which are >10 faster than that of .

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Source
http://dx.doi.org/10.1021/jacs.2c02506DOI Listing

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