Panne, Patricia published the artcileCyanide initiated perfluoroorganylations with perfluoroorgano silicon compounds, Name: Trimethyl(perfluorophenyl)silane, the publication is Journal of Fluorine Chemistry (2001), 112(2), 283-286, database is CAplus.
Cyanophenylphosphines, Ph2PCN or PhP(CN)2, do not react with Me3SiCF3 or Me3SiC6F5 in the absence of cyanide ions. Catalytic amounts of ionic cyanides such as [NEt4]CN, [18-crown-6-K]CN or NaCN initiate perfluoroorganylation reactions. The trifluoromethylphosphines, Ph2PCF3 and PhP(CF3)2, as well as the pentafluorophenylphosphines, Ph2PC6F5 and PhP(C6F5)2, are isolated in 60-75% yield. In DMF or acetone solutions, side reactions are observed while reactions in CH2Cl2 and MeCN proceed selectively. Me3SiCF3 addition to the carbonyl groups of DMF and acetone occurs on treatment of Me3SiCF3 solutions of these solvents with catalytic amounts of cyanide, cyanate or thiocyanate salts even at low temperature The formation of the reactive silicate [Me3Si(CN)CF3]– in reactions with an excess of [18-crown-6-K]CN is proved by low temperature NMR studies.
Journal of Fluorine Chemistry 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 C9H9F5Si, Name: Trimethyl(perfluorophenyl)silane.
Referemce:
https://courses.lumenlearning.com/boundless-chemistry/chapter/catalysis/,
Catalysis – Wikipedia