Stepanov, A. A. published the artcileElectrochemical silylation of unsaturated organofluoric compounds, Related Products of catalysis-chemistry, the publication is Russian Journal of Electrochemistry (Translation of Elektrokhimiya) (2000), 36(2), 190-192, database is CAplus.
Organofluoric compounds are electrolyzed in a diaphragm-less cell filled with aprotic solvent containing trimethylchlorosilane. The following substances are trimethylsilylated in the electrolysis: C6F6, C6F5Cl, C6F5H, C6F5CF3, C5F5N, CFCl:CFCl, and CF2:CFBr, with the introduction of one trimethylsilyl group. The silylation mechanism is established. In some cases, the silylation product yield is increased on a Cu cathode.
Russian Journal of Electrochemistry (Translation of Elektrokhimiya) published new progress about 1206-46-8. 1206-46-8 belongs to catalysis-chemistry, auxiliary class Organic Silicones, name is Trimethyl(perfluorophenyl)silane, and the molecular formula is C17H18N3NaO3S, Related Products of catalysis-chemistry.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia