Nagendiran Anuja, Pascanu Vlad, Bermejo Gómez Antonio, González Miera Greco, Tai Cheuk-Wai, Verho Oscar, Martín-Matute Belén, Bäckvall Jan-E
Department of Organic Chemistry and, Berzelii Centre EXSELENT on Porous Materials, Arrhenius Laboratory, Stockholm University, 106 91, Stockholm, Sweden.
AstraZeneca Translational Science Center at Karolinska Institute, 171 65, Stockholm, Sweden.
Chemistry. 2016 May 17;22(21):7184-9. doi: 10.1002/chem.201600878. Epub 2016 Apr 25.
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: Pd(0) -MIL-101-NH2 (Cr)), 2) nano-Pd on a siliceous mesocellular foam (MCF: Pd(0) -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 Pd(0) -MIL-101-NH2 (Cr) and Pd(0) -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.
据报道,使用负载型钯纳米颗粒可对多种α,β-不饱和羰基化合物中的C=C键进行化学选择性还原。使用1个大气压的氢气对三种不同的多相催化剂进行了比较:1) 金属有机框架上的纳米钯(MOF:Pd(0)-MIL-101-NH2(Cr)),2) 硅质介孔泡沫上的纳米钯(MCF:Pd(0)-AmP-MCF),以及3) 市售的钯碳(Pd/C)。初步研究表明,与市售的Pd/C相比,Pd@MOF和Pd@MCF纳米催化剂在活性和选择性方面更具优势。Pd(0)-MIL-101-NH2(Cr)和Pd(0)-AmP-MCF都能够在非常短的反应时间(10 - 90分钟)内,以低负载量的Pd(0.5 - 1摩尔%)得到所需产物。此外,这两种催化体系表现出高可回收性和极低水平的金属浸出。