首页> 外文期刊>Journal of the Chemical Society, Dalton Transactions. Inorganic Chemistry >Ligand-assisted O-dealkylation of bis(bipyridyl) ruthenium(II) phosphine-ether complexes
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Ligand-assisted O-dealkylation of bis(bipyridyl) ruthenium(II) phosphine-ether complexes

机译:双(联吡啶)钌(II)膦-醚配合物的配体辅助O-脱烷基

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The preparation and characterization of three [Ru(bpy)(2)(POR-P,O)](PF6)(2) complexes are reported where POR = 2-methoxyphenyldiphenylphosphine in 1, 2-ethoxyphenyldiphenylphosphine in 2 and 2-methoxyethyldiphenylphosphine in 3. Complexes 1 and 2 undergo ligand-assisted O-dealkylation by the same weakly basic phosphines, a reaction typically observed for complexes containing highly basic phosphines with multiple ether substituents. The electron deficiency of the Ru(II) centre in these complexes is likely responsible for how readily they are dealkylated to yield the aryloxide complexes. Complex 3 is not susceptible to ligand-assisted dealkylation, primarily because the lower steric demand of its phosphine-ether ligand permits the thermodynamically favoured direct attack of phosphines at the Ru centre. [References: 33]
机译:报道了三种[Ru(bpy)(2)(POR-P,O)](PF6)(2)配合物的制备和表征,其中POR = 1中的2-甲氧基苯基二苯基膦,2中的2-乙氧基苯基二苯基膦,以及2中的2-甲氧基乙基二苯基膦。 3.配合物1和2通过相同的弱碱性膦经历配体辅助的O-脱烷基化,对于包含具有多个醚取代基的高度碱性膦的配合物,通常观察到该反应。这些络合物中Ru(II)中心的电子缺乏可能是导致它们脱烷基化以生成芳基氧化物络合物的难易程度的原因。配合物3不易受配体辅助的脱烷基作用,主要是因为其膦-醚配体的较低空间需求允许膦在Ru中心受到热力学上的直接攻击。 [参考:33]

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