Highly Selective Hydrogenation of Nitriles to Primary Amines without an Additive Using Nanoscale Ni⁰-Ni^II/III-bTiO₂...

Despite significant progress in the catalytic hydrogenation of nitriles, the persistent challenge of requiring additives to prevent condensation byproducts and achieve selectivity toward primary amines demands urgent attention. In this work, we present an integrated approach utilizing a ligand-bridged Ni-Ti bimetallic complex as a precursor to tune Ni⁰-NiO-NiO(OH) heterojunctions and phases of black titania (bTiO₂) by controlling pyrolytic conditions. This tailored phase distribution and charge dynamics across heterojunctions create an effective balance of acidic and basic sites, enabling the direct hydrogenation of nitriles to primary amines without the need for additives. However, at elevated pyrolysis temperatures, this balanced composition begins to shift, with the loss of critical phases that alter the catalyst's structural and chemical properties. This shift reduces amphoteric behavior, resulting in decreased selectivity for primary amines and favoring the formation of condensation byproducts. The catalyst's structure, amphoteric nature, crystallinity, surface area, and active sites are comprehensively characterized using high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), powder X-ray diffraction (PXRD), Fourier-transform infrared spectroscopy (FT-IR), temperature programmed desorption of ammonia (NH₃-TPD), temperature programmed desorption of carbon dioxide (CO₂-TPD), and CO₂ adsorption techniques. The magnetically retrievable catalyst exhibited excellent functional group tolerance, high selectivity, multiple reusability, broad substrate scope, and high activity for nitrile hydrogenation to primary amines, with the potential for advanced catalytic hydrogenation of other functional groups.