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Redox Non-Innocence and Isomer-Specific Oxidative Functionalization of Ruthenium-Coordinated β-Ketoiminate

Sudip Kumar Bera, Sanjib Panda, Sourajit Dey Baksi, Goutam Kumar Lahiri

Chem Asian J. 2019 Dec 2;14(23):4236-4245.

PMID: 31568672

Abstract:

This article deals with isomeric ruthenium complexes [RuIII (LR )2 (acac)] (S=1/2) involving unsymmetric β-ketoiminates (AcNac) (LR =R-AcNac, R=H (1), Cl (2), OMe (3); acac=acetylacetonate) [R=para-substituents (H, Cl, OMe) of N-bearing aryl group]. The isomeric identities of the complexes, cct (cis-cis-trans, blue, a), ctc (cis-trans-cis, green, b) and ccc (cis-cis-cis, pink, c) with respect to oxygen (acac), oxygen (L) and nitrogen (L) donors, respectively, were authenticated by their single-crystal X-ray structures and spectroscopic/electrochemical features. One-electron reversible oxidation and reduction processes of 1-3 led to the electronic formulations of [RuIII (L)(L⋅ )(acac)]+ and [RuII (L)2 (acac)]- for 1+ -3+ (S=1) and 1- -3- (S=0), respectively. The triplet state of 1+ -3+ was corroborated by its forbidden weak half-field signal near g≈4.0 at 4 K, revealing the non-innocent feature of L. Interestingly, among the three isomeric forms (a-c in 1-3), the ctc (b in 2 b or 3 b) isomer selectively underwent oxidative functionalization at the central β-carbon (C-H→C=O) of one of the L ligands in air, leading to the formation of diamagnetic [RuII (L)(L')(acac)] (L'=diketoimine) in 4/4'. Mechanistic aspects of the oxygenation process of AcNac in 2 b were also explored via kinetic and theoretical studies.

Chemicals Related in the Paper:

Catalog Number Product Name Structure CAS Number Price
AP14284936 Ruthenium(III) acetylacetonate Ruthenium(III) acetylacetonate 14284-93-6 Price
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