2025-06-132025-06-132025Molinillo, P., Gálvez Del Postigo, A., Puyo, M., Vattier Lagarrigue, M.F., Beltrán, A.M., Rendón Márquez, N.,...,Suárez, A. (2025). Selective H/D Exchange in E–H (E = Si, Ge, Sn) Bonds Catalyzed by 1,2,3-Triazolylidene-Stabilized Nickel Nanoparticles. Inorganic Chemistry, 64 (16), 8125-8134. https://doi.org/10.1021/acs.inorgchem.5c00216.0020-16691520-510Xhttps://hdl.handle.net/11441/174316Nickel nanoparticles (Ni·MIC) stabilized with mesoionic 1,2,3-triazolylidene (MIC) ligands were prepared via decomposition of the [Ni(COD)2] (COD = 1,5-cyclooctadiene) complex with H2 (3 bar) in the presence of 0.2 or 0.5 equiv of ligand. The obtained monodisperse and small-sized (3.2–3.8 nm) nanoparticles were characterized by high-resolution transmission electron microscopy (TEM, HRTEM) and inductively coupled plasma (ICP) analysis. Further analysis of the nickel nanoparticles by X-ray photoelectron spectroscopy (XPS) demonstrated the coordination of the MIC ligands to the metal surface. Finally, the Ni·MIC nanoparticles were applied in the isotopic H/D exchange in hydrides of group 14 elements (Si, Ge, Sn) using D2 gas under relatively mild conditions (1.0–1.8 mol % Ni, 1 bar D2, 55 °C). High and chemoselective deuterium incorporation at the E–H (E = Si, Ge, Sn) bond in these derivatives was observed.application/pdf10 p.engAttribution 4.0 Internationalhttp://creativecommons.org/licenses/by/4.0/Hydrogen isotopesLigandsNanoparticlesTransmission electron microscopyX-ray photoelectron spectroscopyinfo:eu-repo/semantics/articleinfo:eu-repo/semantics/embargoedAccess10.1021/acs.inorgchem.5c00216