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Mild and Selective Catalytic Hydrogenation of the C=C Bond in a,b-Unsaturated Carbonyl Compounds Using Supported Palladium Nanoparticles

机译:使用负载的钯纳米粒子对a,b-不饱和羰基化合物中C = C键进行轻度和选择性催化加氢

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摘要

Chemoselective reduction of the C=C bond in a variety of α,β-unsaturated carbonyl compounds using supported palladium nanoparticles is reported. Three different heterogeneous catalysts were compared using 1 atm of H2: 1) nano-Pd on a metal–organic framework (MOF: Pd0-MIL-101-NH2(Cr)), 2) nano-Pd on a siliceous mesocellular foam (MCF: Pd0-AmP-MCF), and 3) commercially available palladium on carbon (Pd/C). Initial studies showed that the Pd@MOF and Pd@MCF nanocatalysts were superior in activity and selectivity compared to commercial Pd/C. Both Pd0-MIL-101-NH2(Cr) and Pd0-AmP-MCF were capable of delivering the desired products in very short reaction times (10–90 min) with low loadings of Pd (0.5–1 mol %). Additionally, the two catalytic systems exhibited high recyclability and very low levels of metal leaching.
机译:报道了使用负载的钯纳米颗粒化学选择性还原各种α,β-不饱和羰基化合物中的C = C键。使用1 atm的H2对三种不同的非均相催化剂进行了比较:1)在金属-有机骨架上的纳米钯(MOF:Pd0-MIL-101-NH2(Cr)),2)在硅质中孔泡沫(MCF)上的纳米钯:Pd0-AmP-MCF),和3)商用钯/碳(Pd / C)。初步研究表明,与商用Pd / C相比,Pd @ MOF和Pd @ MCF纳米催化剂的活性和选择性更高。 Pd0-MIL-101-NH2(Cr)和Pd0-AmP-MCF都能够在很短的反应时间内(10-90µmin)以较低的Pd含量(0.5-1%mol%)提供所需的产物。另外,这两种催化体系显示出高的可回收性和非常低的金属浸出率。

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