659720-45-3

Upstream product

• 659720-39-5 [Cp(*)RuCl(CO)(PMe(i)Pr₂)] 
• 79060-88-1 sodium tetrakis[(3,5-di-trifluoromethyl)phenyl]borate 
• 67-64-1 acetone 

Downstream Products

• 659720-41-9 [((C5(CH3)5)Ru(CO)(P(CH3)(CH(CH3)2)2))2(μ-Cl)](tetrakis(3,5-bis(trifluoromethyl)phenyl)borate) 
• 766552-31-2 [Cp(*)Ru=C=CH₂(CO)(PMe(i)Pr₂)][B(3,5-C₆H₃(CF₃)2)4] 
• 766552-23-2 [Cp(*)Ru=C=CHCPh(CO)(PMe(i)Pr₂)][B(3,5-C₆H₃(CF₃)2)4] 

Relevant academic research and scientific papers

Preparation and reactivity of organometallic complexes bearing the fragment Cp*Ru(CO)(PR3) (PR3 = PMeiPr2, PEt3): (see abstract)

The reactions of [Cp*RuCl(CO)(PMeiPr2)] (1) and [Cp*RuCl(CO)(PEt3)] (2) with NaBAr′4 in fluorobenzene both under argon and under dinitrogen generate the binuclear compounds [{Cp*Ru(CO)(PMeiPr2)}2(μ-Cl)] [BAr′4] (3) and [{Cp*Ru(CO)(PEt3)}2(μ-CL)] [BAr′4] (4), respectively, which were fully characterized. The crystal structure of compound 4 is reported, showing for the first time two chiral Cp*Ru fragments bonded through only one bridging chloride ligand. No dinitrogen complexes or 16-electron species could be isolated. Halide abstraction from 1 using dry acetone as solvent yields the compound [Cp*Ru(CO){η1-OC-(CH3)2} (PMeiPr2)][BAr′4] (5). A range of olefins react with [Cp*RuCl(CO)(PMeiPr2)] and NaBAr′4 furnishing the corresponding cationic η2-alkene complexes [Cp*Ru(CO)(L)(PMei-Pr2)][BAr′4] (L = C2H4, 6; H2C=CHPh, 7; and H2C=CHCOOCH3, 8), which are stable under argon atmosphere in solution. The crystal structure of compound 6 is also reported. Both 1 and 2 react with SnCl2 in CH2Cl2 to yield the insertion derivatives [Cp*Ru(CO)(SnCl3)-(PR3)] (PR3 = PMeiPr2, 9; PEt3, 10), which have also been characterized.