Ceria-supported copper nanoparticles: A highly efficient and recyclable catalyst for N-arylation of indole

被引:26
|
作者
Amadine, Othmane [1 ,2 ]
Maati, Houda [1 ,2 ]
Abdelouhadi, Karima [3 ]
Fihri, Aziz [1 ]
El Kazzouli, Said [1 ]
Len, Christophe [4 ,5 ]
El Bouari, Abdeslam [6 ]
Solhy, Abderrahim [1 ,7 ]
机构
[1] MASCIR Fdn, Rabat Design, Rabat 10100, Morocco
[2] Univ Hassan II Mohammedia, FST, Mohammadia 20650, Morocco
[3] Allal Fassi FAR, Div UATRS, CNRST, Rabat 10000, Morocco
[4] Ctr Rech Royallieu, UTC ESCOM, F-60205 Compiegne, France
[5] Univ Hull, Dept Chem, Kingston Upon Hull HU6 7RX, N Humberside, England
[6] Univ Hassan II Mohammedia, Fac Sci Ben MSik, Lab Physicochim Mat Appl, Casablanca, Morocco
[7] Mohammed VI Polytech Univ, Ben Guerir 43150, Morocco
关键词
Nanocatalysis; Ceria; Cu-catalyzed; N-arylation; Indole; GAS SHIFT REACTION; C-N; ARYLBORONIC ACIDS; ARYL HALIDES; IN-SITU; NITROGEN-HETEROCYCLES; NANOCRYSTALLINE CEO2; COUPLING REACTIONS; AEROBIC OXIDATION; BOND FORMATION;
D O I
10.1016/j.molcata.2014.08.009
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Cu@CeO2 catalytic nanomaterials have been synthesized by impregnation of ceria by copper acetate, followed by reduction and calcination under nitrogen. The components of these nanomaterials were characterized by means of XRD, XPS, N-2 adsorption/desorption, TGA, SEM, and TEM microscopy techniques. The XRD spectra of ceria and Cu@CeO(2-)1 (3.4 wt% copper loading) revealed a slight shift of the position of the planes with a small increase of the crystal lattice parameters, which can be explained by an eventual insertion of Cu-0 in interstitial sites and/or a partial substitution of Ce4+ by Cu2+center dot Cu@CeO2 nanomaterials were found to be efficient catalysts for the N-arylation of indole with various aryl bromides to produce good yields of the desired products. The decrease in the catalytic activity of the catalyst during the reuse was probably due to oxidation of Cu-0 to Cu2+ and its poisoning of KBr that was formed in situ. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:409 / 419
页数:11
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