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首页> 外文期刊>New Journal of Chemistry >Nickel(II) complex covalently anchored on core shell structured SiO2@Fe3O4 nanoparticles: a robust and magnetically retrievable catalyst for direct one-pot reductive amination of ketones
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Nickel(II) complex covalently anchored on core shell structured SiO2@Fe3O4 nanoparticles: a robust and magnetically retrievable catalyst for direct one-pot reductive amination of ketones

机译:共价锚固在核壳结构的SiO2 @ Fe3O4纳米颗粒上的镍(II)配合物:一种健壮且可磁性回收的催化剂,用于酮的一锅直接还原胺化

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摘要

A robust and efficient core shell structured magnetically retrievable nickel nanocatalytic system was fabricated via the covalent immobilization of 2-acetyl furan on the surface of an amine functionalized silica coated magnetic nanosupport followed by its metallation with nickel acetate. The newly synthesized magnetic silica based organic-inorganic hybrid nanocatalyst (Ni-ACF@Am-SiO2@Fe3O4) was systematically affirmed using several physico-chemical characterization tools such as FT-IR, XRD, VSM, SEM, TEM, EDS, ED-XRF and AAS. Thereafter, the catalytic performance of this Ni-ACF@Am-SiO2@Fe3O4 nanocatalyst was investigated in the one-pot reductive amination of ketones using NaBH4 as the reductant under neat conditions. The developed core shell magnetic silica based nickel nanocatalyst successfully afforded a structurally diverse range of secondary amines with high turnover frequency (TOF) and excellent conversion percentage. Additionally, it was found that this catalyst could not only be retrieved from the reaction vessel within a fraction of seconds using an external magnet but also be recycled for multiple runs without any discernible loss in its activity that rendered this protocol superior to all the previously established methodologies for the one-pot synthesis of substituted amines. Besides, some of the other fascinating features of this methodology that made it a potential candidate for addressing various economic and environmental concerns were ambient reaction conditions, broad substrate scope, simple workup procedure, shorter reaction time and cost effectiveness.
机译:通过将2-乙酰基呋喃共价固定在胺官能化的二氧化硅包覆的磁性纳米载体表面,然后用乙酸镍进行金属化,制得了坚固而有效的核壳结构磁性可回收镍纳米催化系统。使用多种物理化学表征工具,如FT-IR,XRD,VSM,SEM,TEM,EDS,ED-ED,系统地确认了新合成的磁性二氧化硅基有机-无机杂化纳米催化剂(Ni-ACF @ Am-SiO2 @ Fe3O4)。 XRF和AAS。此后,在纯净条件下,使用NaBH4作为还原剂,在酮的一锅还原胺化反应中研究了该Ni-ACF @ Am-SiO2 @ Fe3O4纳米催化剂的催化性能。开发的核壳磁性二氧化硅基镍纳米催化剂成功提供了结构多样的仲胺,具有高周转频率(TOF)和出色的转化率。另外,发现该催化剂不仅可以使用外部磁体在几秒钟之内从反应容器中回收,而且可以循环多次运行而没有任何明显的活性损失,从而使该方案优于以前建立的所有方案一锅合成取代胺的方法学此外,该方法的其他一些引人入胜的特征使它成为解决各种经济和环境问题的潜在候选者,包括环境反应条件,广泛的底物范围,简单的后处理程序,较短的反应时间和成本效益。

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