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首页> 外文期刊>Catalysis science & technology >Efficient three-component coupling reactions catalyzed by Cu°-nanoparticles stabilized on modified montmorillonite
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Efficient three-component coupling reactions catalyzed by Cu°-nanoparticles stabilized on modified montmorillonite

机译:有效的三组分偶联反应由Cu° - 纳米颗粒催化的改良蒙脱石稳定

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摘要

The in situ generation of Cu°-nanoparticles into the nanopores of modified montmorillonite and their catalytic performance in the three component (A3) coupling reactions of aldehyde, amine and alkyne to synthesize propargylamines have been described here. The modification of montmorillonite was carried out with HCl under controlled conditions for generating nanopores into the matrix and these pores act as a "host" for the in situ generation of Cu°-nanoparticles, The Cu°-nanoparticles were generated in the nanopores of the acid activated clay mineral matrix by the successful loading of a Cu(CH3COO)2 metal precursor using an incipient wetness impregnation technique followed by reduction with NaBH4. The TEM study reveals that Cu°-nanoparticles of below 10 nm in size are evenly distributed on the support. The synthesized Cu°-nanoparticles exhibit a face centered cubic (fcc) lattice. The Cu°-nanoparticles serve as an efficient green and heterogeneous catalyst for three-component coupling via C-H alkyne-activation to synthesize propargylamines with excellent yields (82-94%) and 100% selectivity under mild reaction conditions without requiring any additives or an inert atmosphere. The nanocatalysts can be recycled and reused several times without significant loss of their catalytic activity.
机译:这里已经描述了甲醛,胺和碱在三个成分(A3)偶联反应中合成propargylamines的三个成分(A3)偶联反应中的cu° - 纳米颗粒及其在三个成分(A3)偶联反应中的催化性能。在受控条件下,用HCL对蒙脱石的修饰进行了修饰,以使纳米孔生成基质,这些孔充当了原位cu° - 纳米颗粒的“宿主”,Cu° - 纳米颗粒是在纳米粒子中产生的。酸通过使用初期湿度浸渍技术成功加载Cu(CH3COO)2金属前体激活粘土矿物基质,然后用​​NaBH4还原。 TEM研究表明,大小低于10 nm的Cu° - 纳米颗粒在支撑上均匀分布。合成的Cu° - 纳米颗粒表现出面部中心立方(FCC)晶格。 Cu° - 纳米颗粒用作有效的绿色和异质催化剂,可通过C-H炔烃激活进行三组分耦合,以使proparyamines具有出色的收益率(82-94%)(82-94%)和100%选择性,而无需任何添加剂或惰性反应条件下气氛。纳米催化剂可以回收并重复多次,而不会显着丧失其催化活性。

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