PdCl2-2,6-bis(1,5-diphenyl-1H-pyrazol-3-yl)pyridine catalyzed Suzuki–Miyaura cross-coupling
作者:Qin Yang、Lei Wang、Lei Lei、Xue-Li Zheng、Hai-yan Fu、Mao-lin Yuan、Hua Chen、Rui-Xiang Li
DOI:10.1016/j.catcom.2012.10.009
日期:2012.12
Six multidentate nitrogen ligands, 2,6-bis(1,5-diphenyl-1H-pyrazol-3-yl)pyridine (L1), 2,6-bis(1-methyl-5-phenyl-1H-pyrazol-3-yl)pyridine (L2), 2,6-bis(1,5-dimethyl-1H-pyrazol-3-yl)pyridine (13), 2,6-bis(5-phenyl-1H-pyrazol-3-yl)pyridine (L4), 2,6-bis(1-p-triflurophenyl-5-phenyl-1H-pyrazol-3-yl)pyridine (L5), and 2,6-bis(1-m-methylphenyl-5-phenyl-1H-pyrazol-3-yl)pyridine (16) were synthesized and characterized. Their palladium complexes catalyzed Suzuki-Miyaura cross-coupling revealed that the catalytic activities of these complexes were in the order of PdCl2-L5>PdCl2-L1>PdCl2-L6>PdCl2-L2>PdCl2-L3>PdCl2-L4. With a low Pd loading of 10(-5) mol%, PdCl2-L1 showed a high activity. The turnover numbers (TONs) were up to 58,000,000 for 4-bromobenzotrifluoride. (C) 2012 Elsevier B.V. All rights reserved.