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Synthesis and Reactivity of Hybrid Phosphido- and Hydrosulfido-Bridged Diruthenium Complexes: Transformations into Diruthenium and Tetraruthenium Complexes Bridged by Phosphido and Sulfido Ligands
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文摘
The reaction of the monophosphido-bridged diruthenium(III) complex [Cp*RuCl(渭-PMe2)(渭-Cl)RuClCp*] with sodium hydrogen sulfide affords the hybrid phosphido- and hydrosulfido-bridged diruthenium(III) complex [Cp*RuCl(渭-PMe2)(渭-SH)RuClCp*]. The hydrosulfido-bridged diruthenium(III) complex can be further converted into the corresponding sulfido-bridged multinuclear ruthenium(III) complex via deprotonation of the hydrosulfido ligand. The hydrosulfido-bridged diruthenium(III) complex also reacts with bases to afford a coordinatively unsaturated diruthenium(III) complex, where insertion of terminal alkynes further occurs to form phosphido-bridged diruthenium(III) complexes bearing ruthenathiacyclobutene moieties.

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