Synthesis and characterization of nano-cellulose immobilized phenanthroline-copper (I) complex as a recyclable and efficient catalyst for preparation of diaryl ethers, N-aryl amides and N-aryl heterocycles

被引:8
作者
Hosseinzadeh, Rahman [1 ]
Aghili, Nora [1 ]
Mavvaji, Mohammad [1 ]
机构
[1] Univ Mazandaran, Fac Chem, Dept Organ Chem, Babolsar, Iran
关键词
Copper nanocatalyst; Functionalized nanocellulose; Diaryl ethers; N-arylation reaction; Coupling reaction; CROSS-COUPLING REACTIONS; HIGHLY EFFICIENT; C-N; ARYLBORONIC ACIDS; NITROGEN-HETEROCYCLES; CUO NANOPARTICLES; H HETEROCYCLES; BENZYL AMINES; O-ARYLATION; HALIDES;
D O I
10.1016/j.poly.2021.115631
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Functionalized nanocellulose was prepared and employed for immobilization of phenanthroline-copper(I) complex to afford cellulose nanofibril grafted heterogeneous copper catalyst [CNF-phen-Cu(I)]. This nano-catalyst was well characterized using FT-IR, NMR, XRD, CHNS, AAS, TGA, EDX and SEM. The activities of the synthesized catalyst were examined in the synthesis of diaryl ethers via C-O cross-coupling of phenols and aryl iodides, as well as, the preparation of N-aryl amides and N-aryl heterocycles through C-N cross-coupling of amides and N-H heterocycle compounds with aryl halides. In this trend, various substrates containing electron-donating and electron-withdrawing groups were exploited to evaluate the generality of this catalytic protocol. Accordingly, the catalyst demonstrated remarkable catalytic efficiency for both C-N and C-O cross-coupling reactions, thereby resulting in good to excellent yields of the desired products. Furthermore, the recover-ability experiments of the catalyst showed that it can be readily retrieved by simple filtration and successfully reused several times with negligible loss of its catalytic activity.
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页数:11
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