化学
钯
碘化物
溴化物
离子液体
芳基
催化作用
离子键合
反应性(心理学)
赫克反应
三氟甲磺酸
药物化学
晶体结构
无机化学
高分子化学
结晶学
有机化学
离子
烷基
替代医学
病理
医学
作者
Francisco R. Fortea-Pérez,Isabel Schlegel,Miguel Julve,Donatella Armentano,Giovanni De Munno,Salah‐Eddine Stiriba
标识
DOI:10.1016/j.jorganchem.2013.06.041
摘要
New and versatile bis(oxamato)palladate(II) complexes of formula (n-Bu4N)2[Pd(2-Mepma)2]·4H2O (1a) and (n-Bu4N)2[Pd(4-Mepma)2]·2H2O·MeCN (1b) (n-Bu4N+ = tetra-n-buthylammonium, 2-Mepma = N-2-methylphenyloxamate and 4-Mepma = N-4-methylphenyloxamate) have been synthesized and characterized by spectroscopic methods and single crystal X-ray diffraction. Each palladium(II) ion in 1a and 1b is four-coordinate with two oxygen and two nitrogen atoms from two fully deprotonated oxamate ligands building a centrosymmetric square planar surrounding. Their catalytic role has been investigated for both Heck and Suzuki coupling reactions using a series of aryl iodide/bromide derivatives in tetra-n-butylammonium bromide (n-Bu4NBr) as ionic liquid, i.e. molten salt. These precatalysts appear as highly efficient, easily recovered and reused at least eight times without any drastic loss of their exceptional reactivity or leaching from the ionic liquid medium.
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