Some scientific research about Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II)

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Synthetic Route of 32993-05-8, An article , which mentions 32993-05-8, molecular formula is C41H35ClP2Ru. The compound – Chlorocyclopentadienylbis(triphenylphosphine)ruthenium(II) played an important role in people’s production and life.

The complex [CpRu(eta6-naphthalene)]PF6 (2) is a readily accessible and air-stable source of the CpRu+ fragment (Cp = eta5C5H5) for applications in complex synthesis and catalysis. The utility of this precursor complex is demonstrated in a number of experiments: The counterion of 2 is exchanged by reaction with cinchonidinium A-TRISPHAT to give [CpRu(eta6-naphthalene)]A- TRISPHAT (4; with X-ray crystal structure). Ligand exchange of 2 in acetonitrile with (Z,Z)- 1,5-cyclooctadiene (COD) produces [CpRu(eta2: eta2-COD)(MeCN)]PF6 (5; with X-ray crystal structure); with chelating phosphanes (P-P), complexes [CpRu(P-P)(MeCN)]PF6 are selectively generated, and starting with a 1,4-diazadiene, a solvento complex [CpRu(diazadiene-N,N?)(MeCN)]PF6 is obtained. Stepwise reaction of 2 (or 4) in acetonitrile with different monodentate phosphanes PR3 and PR’3 first gives [CpRu(PR 3)(MeCN)2]+ (I), then the chiral-at-metal cation [CpRu(PR3)(PR’3)(MeCN)]+ (II), which was resolved spectroscopically (31P NMR) when combined with the enantiopure Delta-TRISPHAT counterion. Complex cations of type I or II incorporating 2-diphenylphosphinopyridines as ligands display either the eta1-p or the chelating eta2-P,N coordination mode, depending on the size of the ligand and, in solution, the solvent. Reaction of 2 with 3 equiv of triarylphosphanes (PR3) in hot acetone gives rise to [CpRu(PR3)3]+, including the previously unknown cation [CpRu(PPh3)3]+. The in situ combination of 2 and 2 equiv of bulky 6-substituted 2-pyridylphosphanes catalyzes the anti-Markovnikov hydration of terminal alkynes to aldehydes. Either complex 2 or 5 catalyzes the [2+2+2]-cycloaddition of COD with alkynes. Complex 5 is a catalyst for the coupling of allyl alcohols with terminal alkynes to give 4-alkenones.

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Reference:
Highly efficient and robust molecular ruthenium catalysts for water oxidation,
Catalysts | Special Issue : Ruthenium Catalysts – MDPI