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tris(pentafluorophenyl)borane

 
National Institutes of Health

Papers overview

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2017
2017
In this work, well-soluble tris(pentafluorophenyl)borane (BCF) is introduced for the first time into 2,2',7,7'-tetrakis(N,N'-di-p… Expand
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Highly Cited
2016
Highly Cited
2016
Catalytic acceptorless dehydrogenation is an environmentally benign way to desaturate organic compounds. This process is… Expand
2013
2013
We report a kinetic and mechanistic study into the one-electron reduction of the archetypal Lewis acid tris(pentafluorophenyl… Expand
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Highly Cited
2012
Highly Cited
2012
We have increased organic field-effect transistor (OFET) NH(3) response using tris(pentafluorophenyl)borane (TPFB) as a receptor… Expand
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Highly Cited
2010
Highly Cited
2010
The frustrated Lewis pair system consisting of 2 equiv of 2,2,6,6-tetramethylpiperidine (TMP) and tris(pentafluorophenyl)borane… Expand
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Highly Cited
2006
Highly Cited
2006
A mixture of a zirconium benzyl phenoxide complex and tris(pentafluorophenyl)borane is reported that catalyzes the hydrosilation… Expand
Highly Cited
2005
Highly Cited
2005
  • G. Erker
  • Dalton transactions
  • 2005
  • Corpus ID: 45309079
Tris(pentafluorophenyl)borane is best known for its role as an excellent activator component in homogeneous Ziegler-Natta… Expand
Highly Cited
2005
Highly Cited
2005
The previously known anion [(C6F5)3B(mu-OH)B(C6F5)3]- (2) has been prepared by a two-step procedure, involving deprotonation of… Expand
Highly Cited
2003
Highly Cited
2003
The ring-opening reactions of nonactivated aziridines with amine nucleophiles are efficiently catalyzed by tris(pentafluorophenyl… Expand
Highly Cited
1999
Highly Cited
1999
The commercially available borane tris(pentafluorophenyl)borane, B(C(6)F(5))(3), is an effective catalyst for the dehydrogenative… Expand