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Mizoroki-Heck reactions catalyzed by palladium dichloro-bis(aminophosphine) complexes under mild reaction conditions. The importance of ligand composition on the catalytic activity

机译:钯二氯-双(氨基膦)配合物在温和的反应条件下催化的Mizoroki-Heck反应。配体组成对催化活性的重要性

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摘要

Dichloro-bis(aminophosphine) complexes of palladium with the general formula [(P{(NC5H_(10))_(3-n)(C6H_(11))_n})2Pcl(CI)2] (where n = 0-2) are easily accessible, cheap and air stable, highly active and universally applicable C-C cross-coupling catalysts, which exhibit an excellent functional group tolerance. The ligand composition of amine-substituted phosphines (controlled by the number of P-N bonds) was found to effectively determine their catalytic activity in the Heck reaction, for which nanoparticles were demonstrated to be their catalytically active form. While dichloro{bis[1,1',1"-(phosphinetriyl)tripiperi-dine]}palladium (1), the least stable complex (towards protons) within the series of [(P{(NC5H_(10))_(3-n)-(C6H_(11))_n})2Pd(CI)2] (where n = 0-3), is a highly active Heck catalyst at 100 °C and, hence, a rare example of an effective and versatile Heck catalyst that efficiently operates under mild reaction conditions (100 °C or below), a significant successive drop in activity was noticed for dichloro-bis(1,1'-(cyclohexylphosphine-diyl)dipiperidine)palladium (2, with n = 1), dichloro-bis(1-(dicyclohexylphosphinyl)piperidine)palladium (3, with n = 2) and dichioro-bis(tricyclohexylphosphine)palladium (4, with n = 3), of which the latter is essentially inactive (at least under the reaction conditions applied). This trend was explained by the successively increasing complex stability and its ensuing retarding effect on the (water-induced) generation of palladium nanoparticles thereof. This interpretation was experimentally confirmed (initial reductions of 1-4 into palladium(O) complexes of the type [Pd(P{(NC5H_(10))_(3-n)(C6H_(11))_n})2] (where n = 0-3) were excluded to be the reason for the activity difference observed as well as molecular (Pd~0/Pd~(II)) mechanisms were excluded to be operative) and thus demonstrates that the catalytic activity of dichloro-bis(amino-phosphine) complexes of palladium can - in reactions where nanoparticles are involved - effectively be controlled by the number of P-N bonds in the ligand system.
机译:通式为[[P {(NC5H_(10))_(3-n)(C6H_(11)_n})2Pcl(CI)2的钯的二氯双(氨基膦)配合物(其中n = 0- 2)易于获得,价格便宜且空气稳定,高活性且通用的CC交叉偶联催化剂,具有出色的官能团耐受性。发现胺取代的膦的配体组成(受P-N键的数量控制)可有效地确定其在Heck反应中的催化活性,对此证明纳米颗粒为其催化活性形式。而二氯{bis [bis [1,1',1“-(膦三基)三哌啶-二胺]}钯(1),在[[P {(NC5H_(10))_( 3-n)-(C6H_(11)_n})2Pd(CI)2](其中n = 0-3)是在100°C时具有高活性的Heck催化剂,因此,这是一个有效且有效的稀有例子多功能Heck催化剂可在温和的反应条件下(100°C或更低)有效运行,对于二氯-双(1,1'-(环己基膦-二基)二哌啶)钯(2,n = 1),二氯双(1-(二环己基膦基)哌啶)钯(3,n = 2)和dichioro-双(三环己基膦)钯(4,n = 3),后者基本上是无活性的(至少这种趋势可以通过复合物稳定性的不断提高及其对钯纳米颗粒(水诱导的)生成的阻滞作用来解释。 1-4还原成[Pd(P {(NC5H_(10))_(3-n)(C6H_(11))_ n})2]类型的钯(O)络合物](其中n = 0-3 )排除了观察到活性差异的原因,同时排除了分子(Pd〜0 / Pd〜(II))的作用机理),从而证明了二氯双(氨基膦)的催化活性在涉及纳米粒子的反应中,钯的配合物可以有效地由配体系统中PN键的数量控制。

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