Mechanistic study on the coupling reaction of aryl bromides with arylboronic acids catalyzed by (iminophosphine)palladium(0) complexes. Detection of palladium(II) intermediate with a coordinated boron anion

摘要

The complexes [Pd(g2-dmfu)(P–N)] [P–N = 2-(PPh2)C6H4-1-CH=NR, R = C6H4OMe-4; CHMe2;udC6H3Me2-2,6; C6H3(CHMe2)-2,6] react with an excess of BrC6H4R1-4 (R1 = CF3; Me) yielding theudoxidative addition products [PdBr(C6H4R1-4)(P–N)] at different rates depending on R [C6H4OMe-4 >udC6H3(CHMe2)-2,6 > CHMe2 ≈ C6H3Me2-2,6] and R1 (CF3 Me). In the presence of K2CO3 andudactivated olefins (ol = dmfu, fn), the latter compounds react with an excess of 4-R2C6H4B(OH)2 (R2 =udH, Me, OMe, Cl) to give [Pd(g2-ol)(P–N)] and the corresponding biaryl through transmetallation andudfast reductive elimination. The transmetallation proceeds via a palladium(II) intermediate with anudO-bonded boron anion, the formation of which is markedly retarded by increasing the bulkiness ofudR. The intermediate was isolated for R = CHMe2, R1 = CF3 and R2 = H. The boron anion isudformulated as a diphenylborinate anion associated with phenylboronic acid and/or as audphenylboronate anion associated with diphenylborinic acid. In general, the oxidative addition proceedsudat a lower rate than transmetallation and represents the rate-determining-step in the coupling reactionudof aryl bromides with arylboronic acids catalyzed by [Pd(g2-dmfu)(P–N)].