Abstract

Several cobalt-containing bulky monodentate phosphines (μ-PPh 2CH 2PPh 2)Co 2(CO) 4(μ,η-( t Bu) 2PC C(C 6H 4R)) ( 4a: R=H; 4b: R= p-F; 4cp: R= p-CF 3; 4cm: R= m-CF 3; 4d: R= p-OMe) were prepared from the reactions of ( t Bu) 2PC C(R–C 6H 4) ( 2a: R=H; 2b: R= p-F; 2cp: R= p-CF 3; 2cm: R= m-CF 3; 2d: R= p-OMe) with Co 2(CO) 6(μ-PPh 2CH 2PPh 2) 3. Further reactions of 4a, 4b, 4cp, 4cm, and 4d with Pd(OAc) 2 yielded unique palladium complexes (μ-PPh 2CH 2PPh 2)Co 2(CO) 4(μ,η-( t Bu) 2PC C(C 6H 3R)-κC 1)Pd(μ-OAc) ( 5a: R=H; 5b: R= p-F; 5cp: R= p-CF 3; 5cm: R= m-CF 3; 5d: R= p-OMe, respectively). The strong electron-withdrawing substituents, –F and –CF 3, assist the ortho-metalation process during the formation of 5b, 5cp, and 5cm. The more positively charged palladium center in 5b (or 5cp, 5cm) enhances the probability for PhB(OH) 3 − to attack the metal center and the rate of reduction thereafter. DFT studies on the charges of these palladium centers support this assumption. The enhancement of the reaction rates of the Suzuki–Miyaura cross-coupling reactions using 5b, 5cp, and 5cm is thereby attributed to this effect.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call