Palladium(II) Complexes with N-Phosphanyl- N-heterocyclic Carbenes as Catalysts for Intermolecular Alkyne Hydroaminations

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Abstract

The catalytic potential of palladium(II) complexes with chelating N-phosphanyl-N-heterocyclic carbenes featuring a saturated imidazolin-2-ylidene or tetrahydropyrimid-2-ylidene ring has been investigated in intermolecular alkyne hydroamination reactions. The complexes were found to be among the most active Pd-based catalysts for these processes and to enable the use of low reaction temperatures (40 °C) and of solventless conditions. The Pd complexes require activation by 2 equiv of a silver salt to remove chlorido ligands from the metal coordination sphere; they can however also be presynthesized in active form, which allows their use under silver-free conditions. The hydroamination reaction was found to efficiently proceed with terminal alkynes and different ring-substituted, primary arylamine substrates.

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Franco, D., Marchenko, A., Koidan, G., Hurieva, A. N., Kostyuk, A., & Biffis, A. (2018). Palladium(II) Complexes with N-Phosphanyl- N-heterocyclic Carbenes as Catalysts for Intermolecular Alkyne Hydroaminations. ACS Omega, 3(12), 17888–17894. https://doi.org/10.1021/acsomega.8b02619

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