Silica-supported silver nanoparticles as an efficient catalyst for aromatic C-H alkylation and fluoroalkylation

被引:30
作者
Khrizanforov, Mikhail N. [1 ]
Fedorenko, Svetlana V. [1 ]
Mustafina, Asiya R. [1 ]
Kholin, Kirill V. [1 ]
Nizameev, Irek R. [1 ]
Strekalova, Sofia O. [1 ]
Grinenko, Valeriya V. [1 ]
Gryaznova, Tatiana V. [1 ]
Zairov, Rustem R. [1 ]
Mazzaro, Raffaello [2 ,3 ]
Morandi, Vittorio [3 ]
Vomiero, Alberto [2 ]
Budnikova, Yulia H. [1 ]
机构
[1] RAS, FRC Kazan Sci Ctr, Arbuzov Inst Organ & Phys Chem, 8 Arbuzov Str, Kazan 420088, Russia
[2] Lulea Univ Technol, Dept Engn Sci & Math, S-97187 Lulea, Sweden
[3] CNR, IMM, Bologna Sect, Via Piero Gobetti 101, I-40139 Bologna, Italy
基金
俄罗斯科学基金会; 欧盟地平线“2020”;
关键词
ORGANIC HALIDES; FLUORINE; TRIFLUOROMETHYLATION; PERFLUOROALKYLATION; AG; FUNCTIONALIZATION; HETEROARENES; ACYLATION; ARYLATION; ALCOHOLS;
D O I
10.1039/c8dt01090k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The efficient catalysis of oxidative alkylation and fluoroalkylation of aromatic C-H bonds is of paramount importance in the pharmaceutical and agrochemical industries, and requires the development of convenient Ag-0-based nano-architectures with high catalytic activity and recyclability. We prepared Ag-doped silica nanoparticles (Ag0/+@SiO2) with a specific nano-architecture, where ultra-small sized silver cores are immersed in silica spheres, 40 nm in size. The nano-architecture provides an efficient electrochemical oxidation of Ag+@SiO2 without any external oxidant. In turn, Ag+@SiO2 5 mol% results in 100% conversion of arenes into their alkylated and fluoroalkylated derivatives in a single step at room temperature under nanoheterogeneous electrochemical conditions. Negligible oxidative leaching of silver from Ag0/+@SiO2 is recorded during the catalytic coupling of arenes with acetic, difluoroacetic and trifluoroacetic acids, which enables the good recyclability of the catalytic function of the Ag0/+@SiO2 nanostructure. The catalyst can be easily separated from the reaction mixture and reused a minimum of five times upon electrochemical regeneration. The use of the developed Ag-0@SiO2 nano-architecture as a heterogeneous catalyst facilitates aromatic C-H bond substitution by alkyl and fluoroalkyl groups, which are privileged structural motifs in pharmaceuticals and agrochemicals.
引用
收藏
页码:9608 / 9616
页数:9
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