A Dimeric Chromium(II) Pincer as an Electron Shuttle for N=N Bond Scission

Abstract

Reduction of the bis-pyrazolyl pyridine complex [CrL]₂ with 4 KC₈ , followed by addition of one azobenzene (overall mole ratio 1:4:1), PhNNPh, transfers reducing equivalents to three azobenzenes, to form [K₃ Cr(PhNNPh)₃ ]. This has three κ² PhNNPh^2- ligands and K⁺ bound to nitrogen atoms of azobenzene. When the stoichiometry is modified to 1:4:3, the product is changed to [K₂ CrL(PhNNPh)₂ ], which has C₂ symmetry except for the intimate ion pairing of two K⁺ ions to reduced azobenzene nitrogen atoms, and to pyrazolate and phenyl rings. The origin of the observed delivery of reducing equivalents to several, not to a single N=N bond, is traced to the resistance of the one-electron-reduced substrate to receiving a second electron, and is thus a general phenomenon. [CrL]₂ alone is shown to be a two-electron reductant towards benzo[c]cinnoline (BCC) resulting in a product of formula [Cr₂ L₂ (BCC)], in which the reducing equivalents originate purely from Cr^II . An analogous study of the reaction of [CrL]₂ with azobenzene yields [Cr₂ L₂ (PhNNPh)(THF)], an adduct in which one THF has displaced one of four hydrazide nitrogen/Cr bonds. Together these illustrate different modes for the Cr₂ L₂ unit to bind and reduce the N=N bond. Collectively, these results show that two divalent Cr, without added K⁰ , have the ability to reduce the N=N bond. Further KC₈ reduction of preformed Cr₂ L₂ (RNNR) inevitably gives products in which K⁺ stabilizes the charge in the increasingly electron-rich nitrogen atoms, in a phenomenon which mimics proton coupled electron transfer: K⁺ performs the role of H⁺ . A least-squares fit of the two singly reduced DFT structures shows that the only major change is a re-orientation of one of the two phenyl rings in order to avoid repulsion with potassium but to still allow interaction of that phenyl π system with K⁺ . This shows both the impact of K⁺ , being modest to nitrogen/chromium interactions, but nevertheless accommodating some π donation of phenyl to potassium. Finally, delivering increasing equivalents of KC₈ leads to complete cleavage of the N=N bond, and both N bind to three Cr^II . The varied impacts of the K⁺ electrophile on NN multiple bond reduction is discussed.

Keywords: CrII; K/arene interaction; N=N cleavage; azobenzene; pincer.