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tris(pentafluorophenyl)borane CAS NO.1109-15-5

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Min.Order Quantity:
5 Gram
Purity:
98%
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T/T

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Product Details

Keywords

  • 1109-15-5
  • battery electrolyte
  • catalyst

Quick Details

  • ProName: tris(pentafluorophenyl)borane
  • CasNo: 1109-15-5
  • Molecular Formula: C5H7N3
  • Appearance: white powder
  • Application: 1109-15-5 widely used in the prepara...
  • DeliveryTime: please inquire
  • PackAge: 5g, 10g, 100g, 500g, 1kg
  • ProductionCapacity: 10 Kilogram/Week
  • Purity: 98%
  • Storage: -5 degree,
  • LimitNum: 5 Gram
  • Grade: Reagent Grade
  • FNMR: FNMR

Superiority

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]

this is a star product which has mature synthesis route and process conditions. after 8 years product promation, we gained quality approval from customers both in domestic and overseas market.

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Details

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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