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Facile Synthesis of Hybrid Core-Shell Nanospheres for the Asymmetric Transfer Hydrogenation of Aromatic Ketones

机译:杂交核 - 壳纳米球的外壳合成,芳香族酮的不对称转移氢化

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摘要

The polymer-inorganic hybrid core-shell nanospheres with N-(para-toluenesulfonyl)-1,2-diphenylethylenediamine in the core and the poly(methyl acrylate) (PMA) polymer in the shell were prepared by using a sol-gel process. The surface properties of solid catalysts were modified by controlling PMA and the cetyltrimethylammonium bromide surfactant in the shell. The water contact angle results suggest that the presence of PMA and cetyltrimethylammonium bromide in the shell increases the surface hydrophobicity. In the Rh-catalyzed transfer hydrogenation of aromatic ketones in aqueous HCOONa, the solid catalyst with higher surface hydrophobicity demonstrates higher activity, which suggests that suitable surface properties increase the reaction rate by increasing the diffusion rates of hydrophobic substrates. Furthermore, this heterogeneous catalyst can be reused conveniently without loss of ee values.
机译:通过使用溶胶 - 凝胶法制备核心中具有N-(甲苯磺酰基)-1,2-二苯基乙二胺的聚合物 - 无机杂化核 - 壳纳米球和壳中的聚(丙烯酸甲酯)(PMA)聚合物。 通过控制壳中的PMA和甲基三甲基铵溴化物表面活性剂来改变固体催化剂的表面性质。 水接触角结果表明,壳中存在PMA和甲烷三甲基溴化铵的存在增加了表面疏水性。 在丙糖酮水溶液中芳香酮的Rh催化转移氢化中,具有较高表面疏水性的固体催化剂表明,通过增加疏水性衬底的扩散速率,提出了合适的表面性能提高了反应速率。 此外,该非均相催化剂可以方便地重复使用而不会损失EE值。

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