T-Bu₃P-Coordinated 2-Phenylaniline-Based Palladacycle Complex/ArBr as Robust Initiators for Controlled Pd(0)/t-Bu₃P-Catalyzed Suzuki Cross-Coupling Polymerization of AB-Type Monomers

t-Bu₃P-coordinated 2-phenylaniline-based palladacycle complex (1) as the unique source of Pd(0)/t-Bu₃P to form efficient initiators with ArBr for controlled Suzuki cross-coupling polymerizations of AB-type monomers was described. The in situ generated initiators were demonstrated to be robust initiator systems for controlled Suzuki cross-coupling polymerization, affording polymers with unprecedentedly narrow PDIs and well-controlled functional end groups. ³¹P NMR study suggested that the fast and efficient generation of ArPd(t-Bu₃P)Br complexes from precatalyst 1 and ArBr might be the reason for better control of polymerization with precatalyst 1/ArBr as initiators. Our study provided a family of unprecedented, highly efficient initiators for controlled Suzuki cross-coupling polymerizations and a direct route to access conjugated polymers with a variety of heterobisfunctional chain end groups.