Efficient Suzuki Coupling of Aryl Chlorides Catalyzed by Palladium(0) with a P,N Heteroligand and Isolation of Unsaturated Intermediates

A mixture of Pd2(dba)3/[η-C5H4CHN(C6H5)]Fe[η-C5H4P(t-Bu)2] (1) efficiently catalyzes the Suzuki
cross-couplings of a range of arylboronic acids and aryl
chlorides, affording the desired biaryl products in high
isolated yields. Two catalytically active Pd(0) intermediates, viz. 16-electron [η-C5H4CHN(C6H5)]Fe[η-C5H4P(t-Bu)2]Pd(dba) (2) and 14-electron linear Pd{[η-C5H4CHN(C6H5)]Fe[η-C5H4P(t-Bu)2]}2 (3) together with an
oxidative addition product are isolated and crystallographically established.