Grupo de Química Organometálica, Departamento de Química Inorgánica, Facultad de Química, Universidad de Murcia, Murcia, 30071 Spain.
Chemistry. 2012 Jun 18;18(25):7780-6. doi: 10.1002/chem.201103679. Epub 2012 May 8.
The complex [Pd(O,N,C-L)(OAc)], in which L is a monoanionic pincer ligand derived from 2,6-diacetylpyridine, reacts with 2-iodobenzoic acid at room temperature to afford the very stable pair of Pd(IV) complexes (OC-6-54)- and (OC-6-26)-[Pd(O,N,C-L)(O,C-C(6)H(4)CO(2)-2)I] (1.5:1 molar ratio, at -55 °C). These complexes and the Pd(II) species [Pd(O,N,C-L)(OX)] and [Pd(O,N,C-L')(NCMe)]ClO(4), (X = MeC(O) or ClO(3), L' = another monoanionic pincer ligand derived from 2,6-diacetylpyridine), are precatalysts for the arylation of CH(2)=CHR (R = CO(2)Me, CO(2)Et, Ph) using IC(6)H(4)CO(2)H-2 and AgClO(4). These catalytic reactions have been studied and a tentative mechanism is proposed. The presence of two Pd(IV) complexes was detected by ESI(+)-MS during the catalytic process. All the data obtained strongly support a Pd(II)/Pd(IV) catalytic cycle.
该复合物 [Pd(O,N,C-L)(OAc)] 中,L 是由 2,6-二乙酰基吡啶衍生而来的单阴离子夹持配体,与 2-碘苯甲酸在室温下反应,得到非常稳定的一对 Pd(IV) 配合物 (OC-6-54)- 和 (OC-6-26)-[Pd(O,N,C-L)(O,C-C(6)H(4)CO(2)-2)I](摩尔比为 1.5:1,在-55°C)。这些配合物以及 Pd(II)物种 [Pd(O,N,C-L)(OX)] 和 [Pd(O,N,C-L')(NCMe)]ClO(4)(X = MeC(O) 或 ClO(3),L' = 另一种由 2,6-二乙酰基吡啶衍生而来的单阴离子夹持配体),是使用 IC(6)H(4)CO(2)H-2 和 AgClO(4)对 CH(2)=CHR(R = CO(2)Me、CO(2)Et、Ph)进行芳基化反应的前催化剂。已经研究了这些催化反应,并提出了一个暂定的机制。在催化过程中,通过 ESI(+)-MS 检测到存在两种 Pd(IV) 配合物。所有获得的数据强烈支持 Pd(II)/Pd(IV) 催化循环。