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tris(pentafluorophenyl)borane

National Institutes of Health

Papers overview

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Review
2017
Review
2017
As main-group chemistry, in particular boron chemistry, has expanded and developed over the past 20 years, one reagent has risen… 
Highly Cited
2017
Highly Cited
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… 
Highly Cited
2016
Highly Cited
2016
Catalytic acceptorless dehydrogenation is an environmentally benign way to desaturate organic compounds. This process is… 
2013
2013
We report a kinetic and mechanistic study into the one-electron reduction of the archetypal Lewis acid tris(pentafluorophenyl… 
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… 
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… 
Highly Cited
2010
Highly Cited
2010
Two new frustrated Lewis acid—base catalyst systems with high reactivity are used in catalytic metal-free hydrogenations. 
Highly Cited
2006
Highly Cited
2006
A mixture of a zirconium benzyl phenoxide complex and tris(pentafluorophenyl)borane is reported that catalyzes the hydrosilation… 
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… 
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…