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Hydride-bridged transition metal complexes have been found to serve as suitable precursors for the activation of small molecules without the use of reducing agents. In this study, we synthesized a dinuclear Mo2H8 complex supported by bulky C5H2tBu3 (Cp) ligands, Cp2Mo2H8 (1), from the reaction of CpMoCl4 with KC8 under H2. The hydrides of complex 1 can be replaced with benzene at 60 °C to afford a μ-benzene complex Cp2Mo2H2(μ-C6H6) (2).

Graphical abstract: A dinuclear Mo2H8 complex supported by bulky C5H2tBu3 ligands

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