N,N'-Diaryldihydrophenazines as Visible-Light Photocatalysts for Anilines' Arylation Using a Dual Photoredox/Ni(II) Cross-Coupling Strategy.

It has been shown that cheap and easily available N,N'-diaryldihydrophenazines can successfully replace Ir(III)- and Ru(II)-based photocatalysts in the dual photoredox/Ni(II) C-N coupling of aryl halides with a wide range of anilines (32 examples). The efficient, operationally simple approach to diarylamines has been elaborated, which is amenable to scaling up via a flow apparatus.

N,N'-Diaryldihydrophenazines as a Sustainable and Cost-Effective Alternative to Precious Metal Complexes in the Photoredox-Catalyzed Alkylation of Aryl Alkyl Ketones.

An inexpensive and highly efficient metal-free alternative to commonly used Ru- and Ir-based catalysts was proposed. It was shown that the new 2,7-di-tert-butyl-5,10-bis(4-trifluoromethylphenyl)-5,10-dihydrophenazine outcompeted the iridium phenylpyridyl complex in photoredox activity in the alkylation of silyl enol ethers yielding aryl alkyl ketones. The reaction occurred under visible light irradiation at room temperature and was also applicable to drug derivatives (ibuprofen and naproxen). In-depth photophysical, electrochemical, and quantum chemical studies showed that the aforementioned N,N-diaryldihydrophenazine exhibited enhanced properties that were essential for the photoredox catalysis (a long-lived triplet excited state, strong reducing ability, high stability of the radical cations formed in single-electron-transfer event, and chemical inertness of the catalyst with respect to reactants). Importantly, the substituted N,N'-diaryldihydrophenazines could be obtained directly from diaryl amines; a facile, easily handled and scaled-up one-pot synthetic procedure was elaborated.

Chameleonic Behavior of the α-Methylcyclopropyl Group and Its Through-Space Interactions: A Route to Stabilized Three Redox States in Diarylnitroxides.

The α-methylcyclopropyl (MCP) group with conformationally dependent electronic properties is suggested as an additional structural "instrument" for stabilization of both open-shell and ionic states of diarylnitroxides, to be used as "ambipolar" redox active materials. New MCP-substituted diphenylnitroxides (fully characterized by electrochemical, spectral, and X-ray data) are the most stable nitroxides of the diaryl type known to date [τ1/2 in benzene exceeds three months (2310 h)]. The radicals are capable to reversible oxidation and reduction, yielding stable oxoammonium cations and aminoxyl anions. DFT investigation of the electronic structure and geometry of the compounds confirmed the conformational switching of the cyclopropyl orientation relative to the adjacent aromatic π system is dependent on the nitroxide's redox state. Additional through-space stabilizing interaction between the π-acceptor orbital of the NO+ moiety and the cyclopropyl "banana" bond orbital was also detected, highlighting its good hyperconjugative ability. The estimated σ(para)MCP value (-0.32) confirms its strong electron-donating properties.