Closed Synthetic Cycle for Nickel-Based Dihydrogen Formation.

Dihydrogen evolution was observed in a two-step protonation reaction starting from a Ni0 precursor with a tripodal N-heterocyclic carbene (NHC) ligand. Upon the first protonation, a NiII monohydride complex was formed, which was isolated and fully characterized. Subsequent protonation yields H2 via a transient intermediate (INT) and an isolable NiII acetonitrile complex. The latter can be reduced to regenerate its Ni0 precursor. The mechanism of H2 formation was investigated by using a deuterated acid and scrutinized by 1 H NMR spectroscopy and gas chromatography. Remarkably, the second protonation forms a rare nickel dihydrogen complex, which was detected and identified in solution and characterized by 1 H NMR spectroscopy. DFT-based computational analyses were employed to propose a reaction profile and a molecular structure of the Ni-H2 complex. Thus, a dihydrogen-evolving, closed-synthetic cycle is reported with a rare Ni-H2 species as a key intermediate.

(CAAC)Pd(py) Catalysts Disproportionate to Pd(CAAC)2.

Palladium complexes with one N-heterocyclic carbene (NHC) and a pyridine ancillary ligand are powerful cross-coupling precatalysts. Herein, we report such complexes with a cyclic (alkyl)(amino)carbene (CAAC) ligand replacing the NHC. We find that the alleged reduced form, (CAAC)Pd(py), disproportionates to the (CAAC)2Pd0 complex and palladium nanoparticles. This notwithstanding, they are potent catalysts in the Buchwald-Hartwig amination with aryl chlorides under mild conditions (60 °C). In the presence of dioxygen, these complexes catalyze the formation of diazenes from anilines. The catalytic activities of the NHC- and CAAC-supported palladium(0) and palladium(II) complexes are similar in the cross-coupling reaction, yet the CAAC complexes are superior for diazene formation.