Reaction of PdCl2 with N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine (bdppmapy) afforded a mononuclear complex [(bdppmapy)PdCl2] (1). Compound 1 was characterized by elemental analysis, IR, 1H, 13C and 31P NMR, electrospray ion mass spectra (ESI-MS) and X-ray single crystal crystallography. The Pd(II) center in 1 is chelated by bdppmapy, showing a cis-square planar geometry. With the assistance of additive Cu2O, complex 1 exhibited good catalytic activity toward the decarboxylative cross-coupling reactions between 4-picolinic acid and aryl bromides. In the presence of only 2 mol% catalyst, a family of 4-aryl-pyridines could be isolated in up to 83% yield.
PdCl2与N,N-bis-(diphenylphosphanylmethyl)-2-aminopyridine (bdppmapy)反应生成单核配合物[(bdppmapy)PdCl2] (1)。化合物1通过元素分析、红外光谱、1H、13C和31P NMR、电喷雾离子质谱(ESI-MS)以及X射线单晶晶体学进行了表征。1中Pd(II)中心被bdppmapy咬合,显示出顺式正方平面几何结构。在添加剂
Cu2O的辅助下,配合物1在4-
吡啶酸与芳基
溴化物之间的去羧交叉偶联反应中表现出良好的催化活性。在仅使用2摩尔%的催化剂的情况下,能够分离出一系列4-芳基
吡啶,产率高达83%。