Breuer, W. published the artcileChemistry of bromine pentafluoride. 3. Reactions of bromine pentafluoride and arylbromine tetrafluoride with N-bases, of arylbromine tetrafluoride with fluoride ions, and the fluorine-aryl monosubstitution reactions on the hexafluorobromate(V) anion, Name: Trimethyl(perfluorophenyl)silane, the publication is Zeitschrift fuer Anorganische und Allgemeine Chemie (1992), 85-91, database is CAplus.
BrF5 forms 1:1 adducts with pyridines in organic solvents. In BrF5-N-base adducts the axial Br-F bond is activated for F-aryl substitution reactions. Arylbromine tetrafluorides resulting from F-aryl monosubstitutions also yield 1:1 adducts with pyridines; in contrast to BrF5 they react with F– under reductive elimination. F-aryl substitutions on [BrF6]– are presented and the influence of the Lewis-acidity of the aryl transfer reagent and its coproduct is discussed.
Zeitschrift fuer Anorganische und Allgemeine Chemie 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