Synthesis, characterization, and catalytic oxidation of ethylbenzene over host (zeolite-Y)/guest (copper(II) complexes of tetraaza macrocyclic ligands) nanocomposite materials

被引:10
作者
Salavati-Niasari, Masoud [1 ,2 ]
Davar, Fatemeh [1 ]
机构
[1] Univ Kashan, Inst Nano Sci & Nano Technol, Kashan, Iran
[2] Univ Kashan, Dept Inorgan Chem, Fac Chem, Kashan, Iran
关键词
Nanocomposite materials; Copper(II); Tetraaza; Zeolite encapsulation; Oxidation of ethylbenzene; NANOSCALE MICROREACTOR-ENCAPSULATION; CARBON ACIDS NITROETHANE; TEMPLATE SYNTHESIS IOPTS; CO/MN CLUSTER COMPLEXES; A-BOTTLE SYNTHESIS; NICKEL(II) COMPLEXES; ZEOLITE-Y; CU(II) COMPLEXES; BETA-ZEOLITE; FORMALDEHYDE;
D O I
10.1080/00958972.2010.510557
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Cu(II) complexes of 14- and 16-membered tetraaza macrocyclic ligands have been encapsulated in nanopores of zeolite-Y by a two-step process in the liquid phase: (1) adsorption of [bis(diamine)copper(II)] (diamine = 1,2-diaminoethane, 1,3-diaminopropane, 1,2-diaminobenzene, and 1,3-diaminobenzene); [Cu(N-N)2]2+-NaY; in the nanopores of the zeolite-Y and (2) in situ condensation of the copper(II) precursor complex with ethylcinnamate. The new host-guest nanocomposite materials were characterized by chemical analysis and spectroscopic methods. The oneato and encapsulated complexes exhibit good catalytic activity in the oxidation of ethylbenzene at 333 K, using tert-butyl hydroperoxide as the oxidant. Acetophenone was the major product though small amounts of o- and p-hydroxyacetophenones were also formed revealing that C-H bond activation takes place both at benzylic and aromatic ring carbon atoms.
引用
收藏
页码:3240 / 3255
页数:16
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