Özdemir, IGök, YGürbüz, NÇetinkaya, EÇetinkaya, B2024-08-042024-08-0420040039-79111532-2432https://doi.org/10.1081/SCC-200036594https://hdl.handle.net/11616/102133Four functionalized bis(benzimidazolium) salts (2a-d) have been prepared and characterized by conventional spectroscopic methods and elemental analyses. A highly effective, easy to handle, and environmentally bengin process for palladium-mediated Suzuki cross-coupling was developed. The in situ prepared three-component system Pd(OAc)(2)/bis(benzimidazolium) bromides (2a-d) and Cs2CO3 catalyzes quantitatively the Suzuki cross-coupling of deactivated aryl chloride in aqueous media.eninfo:eu-repo/semantics/closedAccessSuzukicarbenepalladiumbenz imidazol-2-ylidenearyl chloridesphenylboronic acidSuzuki-Miyaura reaction of unactivated aryl chlorides using benzimidazol-2-ylidene ligandsArticle34224135414410.1081/SCC-2000365942-s2.0-8644290061Q3WOS:000225241500011Q3