Cyclopentadienyl Ruthenium(II) Complexes with Bridging Alkynylphosphine Ligands: Synthesis and Electrochemical Studies

The reaction of CpRuCl(PPh₃)₂] (Cp=cyclopentadienyl) and CpRuCl(dppe)] (dppe=Ph₂PCH₂CH₂PPh₂) with bis‐ and tris‐phosphine ligands 1,4‐(Ph₂PC≡C)₂C₆H₄ ( 1 ) and 1,3,5‐(Ph₂PC≡C)₃C₆H₃ ( 2 ), prepared by Ni‐catalysed cross‐coupling reactions between terminal alkynes and diphenylchlorophosphine, has been investigated. Using metal‐directed self‐assembly methodologies, two linear bimetallic complexes, {CpRuCl(PPh₃)}₂(μ‐dppab)] ( 3 ) and {CpRu(dppe)}₂(μ‐dppab)](PF₆)₂ ( 4 ), and the mononuclear complex CpRuCl(PPh₃)(η¹‐dppab)] ( 6 ), which contains a “dangling arm” ligand, were prepared (dppab=1,4‐bis(diphenylphosphino)ethynyl]benzene). Moreover, by using the triphosphine 1,3,5‐tris(diphenylphosphino)ethynyl]benzene (tppab), the trimetallic {CpRuCl(PPh₃)}₃(μ₃‐tppab)] ( 5 ) species was synthesised, which is the first example of a chiral‐at‐ruthenium complex containing three different stereogenic centres. Besides these open‐chain complexes, the neutral cyclic species {CpRuCl(μ‐dppab)}₂] ( 7 ) was also obtained under different experimental conditions. The coordination chemistry of such systems towards supramolecular assemblies was tested by reaction of the bimetallic precursor 3 with additional equivalents of ligand 2 . Two rigid macrocycles based on cis coordination of dppab to CpRu(PPh₃)] were obtained, that is, the dinuclear complex {CpRu(PPh₃)(μ‐dppab)}₂](PF₆)₂ ( 8 ) and the tetranuclear square {CpRu(PPh₃)(μ‐dppab)}₄](PF₆)₄ ( 9 ). The solid‐state structures of 7 and 8 have been determined by X‐ray diffraction analysis and show a different arrangement of the two parallel dppab ligands. All compounds were characterised by various methods including ESIMS, electrochemistry and by X‐band ESR spectroscopy in the case of the electrogenerated paramagnetic species.