Palladium complex supported on the surface of magnetic Fe(3)O(4) nanoparticles: an ecofriendly catalyst for carbonylative Suzuki-coupling reactions

Diaryl ketone derivatives include well-known compounds with important physiological and biological properties. In order to prepare diaryl ketone derivatives, we constructed a pallidum (0) complex immobilized on Fe(3)O(4) nanoparticles modified with aminobenzoic acid and phenanthroline [Fe(3)O(4)@ABA/Phen-DCA-Pd(0)], and evaluated its catalytic performance for carbonylative Suzuki-coupling reactions of aryl iodides with aryl boronic acid in the presence of Mo(CO)(6) as the CO source under mild conditions. FT-IR, SEM, TEM, EDX, VSM, TGA, XRD, ICP-OES and Elemental mapping techniques were employed to identify the structure of the Fe(3)O(4)@ABA/Phen-DCA-Pd(0) nanocatalyst. Different derivatives of aryl iodides and aryl boronic acids containing withdrawing and donating functional groups were studied for the preparation of diaryl ketones. Also, various derivatives of heteroaryl iodides and boronic acids were used and the desired products were prepared with high yields. The Fe(3)O(4)@ABA/Phen-DCA-Pd(0) nanocatalyst was separated magnetically and reused 7 consecutive times without reducing its catalytic activity. VSM, TEM and ICP-OES spectroscopic techniques confirmed that the synthesized Fe(3)O(4)@ABA/Phen-DCA-Pd(0) catalyst was still stable and maintained its structure despite repeated reuse.