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      Pd nanoparticles immobilized on halloysite decorated with a cyclodextrin modified melamine-based polymer: a promising heterogeneous catalyst for hydrogenation of nitroarenes

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          Abstract

          For the first time, a hybrid system composed of halloysite (Hal) and a cyclodextrin modified melamine-based polymer is developed and employed for immobilization of Pd(0) nanoparticles.

          Abstract

          For the first time, a hybrid system composed of halloysite (Hal) and a cyclodextrin modified melamine-based polymer is developed and employed for immobilization of Pd(0) nanoparticles. The resulting catalytic hybrid system, Pd@HTMC, was then applied as a heterogeneous catalyst for hydrogenation of nitroarenes to the corresponding anilines. The results established that Pd@HTMC could promote hydrogenation under very mild reaction conditions and in a relatively short time. Moreover, investigation of a sterically demanding substrate, nitro-naphthalene, as well as a substrate with a competing functional group, 4-nitroacetophenone, confirmed that the catalyst is capable of hydrogenation of a sterically demanding substrate while selectively hydrogenating the nitro functional group over keto-functionality. The recyclability experiment proved that the catalyst was recyclable up to six reaction runs with a slight loss of the catalytic activity and Pd leaching. Moreover, a hot filtration test confirmed the heterogeneous nature of the catalyst. Finally, the contribution of the cyclodextrin modified melamine-based polymer to the catalysis was confirmed by comparison of the catalytic activity of Pd@HTMC with control catalysts.

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          Control of metal nanocrystal size reveals metal-support interface role for ceria catalysts.

          Interactions between ceria (CeO2) and supported metals greatly enhance rates for a number of important reactions. However, direct relationships between structure and function in these catalysts have been difficult to extract because the samples studied either were heterogeneous or were model systems dissimilar to working catalysts. We report rate measurements on samples in which the length of the ceria-metal interface was tailored by the use of monodisperse nickel, palladium, and platinum nanocrystals. We found that carbon monoxide oxidation in ceria-based catalysts is greatly enhanced at the ceria-metal interface sites for a range of group VIII metal catalysts, clarifying the pivotal role played by the support.
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            Selective Hydrogenation for Fine Chemicals: Recent Trends and New Developments

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              Recyclable Heterogeneous Palladium Catalysts in Pure Water: Sustainable Developments in Suzuki, Heck, Sonogashira and Tsuji-Trost Reactions

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                Author and article information

                Contributors
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                Journal
                NJCHE5
                New Journal of Chemistry
                New J. Chem.
                Royal Society of Chemistry (RSC)
                1144-0546
                1369-9261
                2018
                2018
                : 42
                : 19
                : 15733-15742
                Affiliations
                [1 ]Gas Conversion Department
                [2 ]Faculty of Petrochemicals
                [3 ]Iran Polymer and Petrochemicals Institute
                [4 ]Tehran
                [5 ]Iran
                [6 ]Department of Chemistry
                [7 ]School of Science
                [8 ]Alzahra University
                [9 ]Univ. Artois
                [10 ]CNRS
                [11 ]Centrale Lille
                [12 ]ENSCL
                [13 ]Univ. Lille
                Article
                10.1039/C8NJ03014F
                32d7aa49-88cc-4abe-95b1-6ce81d4b3cc6
                © 2018

                http://rsc.li/journals-terms-of-use

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