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New routes to Cu(I)/Cu rsanocatalysts for the multicomponent click synthesis of 1,2,3-triazoles

机译:到Cu(i)/Cu rsanocatalysts的新路线,用于多组件单击1,2,3-Triazoles的合成

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摘要

An array of copper and copper-zinc based nanoparticles (NPs) have been fabricated employing a variety of polymeric capping agents. Analysis by TEM, XRPD and XPS suggests that by manipulating reagent, reductant and solvent conditions it is possible to achieve materials that are mono-/narrow disperse with mean particle sizes in the =£10 nm regime. Oxidative stability in air is achieved for monometallic NPs using poly(methyl methacrylate) (PMMA) anti-agglomerant in conjunction with a variety of reducing conditions. In contrast, those encapsulated by either poly(1-vinylpyrrolidin-2-one) (PVP) or poly(4-vinylpyridine) (PVPy) rapidly show Cu2O formation, with all data suggesting progressive oxidation from Cu to Cu@Cu2O core-shell structure and finally Cu2O. Bimetallic copper-zinc systems, reveal metal segregation and the formation of Cu2O and ZnO. Catalysts have been screened in the synthesis of 1,2,3-triazoles through multicomponent azide-alkyne 1,3-dipolar cycloaddition. Whereas PMMA- and PVPy-coating results in reduced catalytic activity, those protected by PVP are highly active, with quantitative triazole syntheses achieved at room temperature and with catalyst loadings of 0.03 mol% metal for Cu and CuZn systems prepared using NaH2PO2, N2H4 or NaBH4 reductants.
机译:已经使用各种聚合物封盖剂制造了一系列铜和铜的纳米颗粒(NP)。 TEM,XRPD和XPS的分析表明,通过操纵试剂,还原性和溶剂条件,可以实现具有单个/狭窄分散的材料,其平均粒径在= £10 nm方向上。使用聚(甲基丙烯酸甲酯)(PMMA)抗凝集剂与多种还原条件结合使用聚(PMMA)抗凝集剂,可以实现空气中的氧化稳定性。相反,由聚(1-乙烯基吡咯烷-2-one)(PVP)或聚(4-乙烯基吡啶)(PVPY)封装的那些(PVPY)迅速显示Cu2O的形成,所有数据都表明从Cu@Cu@Cu2O Core-Shell-Shell Shell进行了渐进式氧化结构,最后是Cu2O。双金属铜锌系统,揭示了金属分离以及Cu2O和ZnO的形成。催化剂已通过多组分叠氮化物-alkyne 1,3-二极环加成的1,2,3-三唑进行筛选。而PMMA和PVPY涂层会导致催化活性降低,而受PVP保护的活性高度活跃,在室温下具有定量三唑合成,并且使用NAH2PO2,N2H4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NABH4或NAH2PO2,催化剂负载为0.03 mol%金属。还原剂。

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