1109-15-5 battery electrolyte catalyst
tris(pentafluorophenyl)borane
1109-15-5
B(C6F5)3 is a Lewis acid, stronger than the inorganic parent molecule BF3. In contrast to the prominent Lewis acids, the pentafluorides of the heavier elements of group 15, B(C6F5)3 has no oxidizing properties. B(C6F5)3 forms adducts with neutral and weaker Lewis bases. B(C6F5)3 has the capability to easily accept anionic ligands bonded to metals.
A versatile reagent widely used in the preparation of d0 arene[2] and other organometallic complexes[1][3] useful as polymerization catalysts. Used with tri-tert-butylphosphine (570958) to study the heterolytic cleavage of dihydrogen at room temperature and one atmosphere pressure.[4]
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tris(pentafluorophenyl)borane
1109-15-5
B(C6F5)3 is a Lewis acid, stronger than the inorganic parent molecule BF3. In contrast to the prominent Lewis acids, the pentafluorides of the heavier elements of group 15, B(C6F5)3 has no oxidizing properties. B(C6F5)3 forms adducts with neutral and weaker Lewis bases. B(C6F5)3 has the capability to easily accept anionic ligands bonded to metals.
A versatile reagent widely used in the preparation of d0 arene[2] and other organometallic complexes[1][3] useful as polymerization catalysts. Used with tri-tert-butylphosphine (570958) to study the heterolytic cleavage of dihydrogen at room temperature and one atmosphere pressure.[4]
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