A tetranuclear nickel hydride cluster capable of reversible activation of aromatic and aliphatic C–H bonds
Artikel i vetenskaplig tidskrift, 2026

Metal cluster complexes supported by multiple hydrides are useful for activating inert bonds and molecules, while nickel-based variants capable of activating external substrates remain scarce. Here, we report a tetranuclear Ni-hydride-phosphine cluster, [Ni4H4(PtBu3)4] (1), which we synthesize by reacting [Li(THF)x][Ni{N(SiMe3)2}3] (x ≈ 4.5 − 5) with pinacolborane (HBpin) in the presence of tri-tert-butylphosphine (PtBu3). Its molecular structure features a tetrahedral Ni4 core, with four face-capping μ3-hydrides and four terminally bound PtBu3 ligands. Cluster 1 is capable of reversible C–H and C–D bond cleavage of benzene-d6, toluene-d8, n-octane-d18, and its own PtBu3 ligands at 50 °C, leading to H/D exchange between the deuterated solvents and the ligands in 1. This reactivity is further utilized in the catalytic hydrogen isotope exchange reaction between benzene-d6 and toluene. The reversible dissociation of one PtBu3 ligand in 1 is proposed as the key step to trigger the C–H and C–D bond activation. Quantum chemical computations propose the reversible displacement of one of the PtBu3 ligands in 1 as the key step in triggering C–H and C–D bond activation.

Författare

Kohei Sunami

Kyoto University

Tatsuya Higaki

Kyoto University

Tokyo Metropolitan University

Kanata Tanaka

Kyoto University

Ryotaro Yamanashi

Kyoto University

Chamil Sameera Wickramarachchi Millawalage

Chalmers, Rymd-, geo- och miljövetenskap, Astronomi och plasmafysik

Ryo Takahata

Kyoto University

Toshiharu Teranishi

Kyoto University

Soichi Kikkawa

Tokyo Metropolitan University

Seiji Yamazoe

Tokyo Metropolitan University

Takuya Shiga

University of Tsukuba

Masayuki Nihei

University of Tsukuba

Tatsuhisa Kato

Kyoto University

Hitoshi Izu

Kyoto University

Yasuhiro Ohki

Kyoto University

Nature Communications

2041-1723 (ISSN) 20411723 (eISSN)

Vol. 17 1 7259

Ämneskategorier (SSIF 2025)

Teoretisk kemi

DOI

10.1038/s41467-026-76006-4

Mer information

Senast uppdaterat

2026-08-14