Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of RAS, 8 Arbuzov str., Kazan 420088, Russian Federation.
Dalton Trans. 2018 Jul 24;47(29):9608-9616. doi: 10.1039/c8dt01090k.
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 Ag0-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 Ag0@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.
高效催化芳香族 C-H 键的氧化烷基化和氟烷基化在医药和农化行业中至关重要,需要开发具有高催化活性和可回收性的方便的基于 Ag0 的纳米结构。我们制备了具有特定纳米结构的 Ag 掺杂二氧化硅纳米粒子(Ag0/+@SiO2),其中超小尺寸的银核浸入 40nm 大小的二氧化硅球中。纳米结构提供了一种有效的电化学氧化 Ag+@SiO2 的方法,而无需任何外部氧化剂。反过来,Ag+@SiO2 5mol%在纳米异相电化学条件下,在室温下可一步将芳烃完全转化为其烷基化和氟烷基化衍生物。在芳烃与乙酸、二氟乙酸和三氟乙酸的催化偶联过程中,Ag0/+@SiO2 中银的氧化浸出可以忽略不计,这使得 Ag0/+@SiO2 纳米结构的催化功能具有良好的可回收性。催化剂可以通过电化学再生很容易地从反应混合物中分离出来,并至少重复使用五次。所开发的 Ag0@SiO2 纳米结构用作多相催化剂,可促进芳烃 C-H 键被烷基和氟烷基取代,这些是药物和农化产品中的重要结构基序。