Váňa Jiří, Lang Jan, Šoltésová Mária, Hanusek Jiří, Růžička Aleš, Sedlák Miloš, Roithová Jana
Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 53210 Pardubice, Czech Republic.
Dalton Trans. 2017 Nov 28;46(46):16269-16275. doi: 10.1039/c7dt03832a.
Reactions catalyzed by palladium(ii) acetate and trifluoroacetic acid (TFA) have a clear preactivation phase. However, the structure of real catalytic species remains unclear. We show that the key species are cyclic trinuclear complexes of composition [Pd(OAc)(OTFA)] (x = 1-6) formed by a sequential ligand exchange from [Pd(OAc)]. Furthermore, we prove that the trinuclear palladium backbone of the precatalyst remains preserved during the first phase of the C-H activation reaction of acetanilides. In other words, the reaction pathway including the trinuclear species should be taken into account in discussion about mechanisms of the reactions catalyzed by palladium acetates.
由醋酸钯(II)和三氟乙酸(TFA)催化的反应具有明显的预活化阶段。然而,实际催化物种的结构仍不清楚。我们表明,关键物种是由[Pd(OAc)]通过连续配体交换形成的组成[Pd(OAc)(OTFA)](x = 1 - 6)的环状三核配合物。此外,我们证明了预催化剂的三核钯骨架在乙酰苯胺的C-H活化反应的第一阶段得以保留。换句话说,在讨论醋酸钯催化反应的机理时,应考虑包括三核物种在内的反应途径。