Nitrogen Atom Transfer Catalysis by Metallonitrene C−H Insertion: Photocatalytic Amidation of Aldehydes

Abstract

C−H amination and amidation by catalytic nitrene transfer are well‐established and typically proceed via electrophilic attack of nitrenoid intermediates. In contrast, the insertion of (formal) terminal nitride ligands into C−H bonds is much less developed and catalytic nitrogen atom transfer remains unknown. We here report the synthesis of a formal terminal nitride complex of palladium. Photocrystallographic, magnetic, and computational characterization support the assignment as an authentic metallonitrene (Pd−N) with a diradical nitrogen ligand that is singly bonded to PdII. Despite the subvalent nitrene character, selective C−H insertion with aldehydes follows nucleophilic selectivity. Transamidation of the benzamide product is enabled by reaction with N3SiMe3. Based on these results, a photocatalytic protocol for aldehyde C−H trimethylsilylamidation was developed that exhibits inverted, nucleophilic selectivity as compared to typical nitrene transfer catalysis. This first example of catalytic C−H nitrogen atom transfer offers facile access to primary amides after deprotection.

Square-planar imido complexes of cobalt: synthesis, reactivity and computational study

“…Encouraged by the precedent of cobalt compounds in nitrene chemistry [21][22][23][24][25][26][27][28][29][30][31][32] and the demonstrated ability of pincer ligands to support novel metal imido species, [33][34][35][36][37][38] we turned our focus to the chemistry of the Co(I) compound featuring the pyrrole-based pincer ligand (Scheme 1). 39,40 We have already established the propensity for this species to carry out twoelectron oxidative addition reactions with concomitant bond activation.…”