Tris(pentafluorophenyl)borane

Tris(pentafluorophenyl)borane, sometimes referred to as "BCF", is the chemical compound (C6F5)3B. It is a white, volatile solid. The molecule consists of three pentafluorophenyl groups attached in a "paddle-wheel" manner to a central boron atom; the BC3 core is planar. It has been described as the “ideal Lewis acid” because of its high thermal stability and the relative inertness of the B-C bonds. Related fluoro-substituted boron compounds, such as those containing B\sCF3 groups, decompose with formation of B-F bonds. Tris(pentafluorophenyl)borane is thermally stable at temperatures well over 200 °C, resistant to oxygen, and water-tolerant.

Preparation
Tris(pentafluorophenyl)borane is prepared using a Grignard reagent derived from bromopentafluorobenzene:
 * 3C6F5MgBr + BCl3 → (C6F5)3B + 3MgBrCl

The synthesis originally employed C6F5Li, but this reagent can detonate with elimination of LiF.

Structure
The structure of tris(pentafluorophenyl)borane (BCF) was determined by gas electron diffraction. It has a propeller-like arrangement of its three pentafluorophenyl groups with a torsional angle of 40.6(3)° for the deviation of these groups from a hypothetically planar arrangement. Compared with a torsional angle of 56.8(4)° for, which is a stronger Lewis acid than BCF, this shows that there is some delocalization of electron density from the para-fluorine atoms to the boron atom that reduces its acidity.

Lewis acidity
The most noteworthy property of this molecule is its strong Lewis acidity. Its Lewis acid strength, as quantified by experimental equilibrium constants, is by 7 orders of magnitude higher than the one of structurally analogous triphenylborane. Experimental equilibrium measurements, its AN value (Gutmann-Beckett method) as well as quantum-chemical calculations all indicate that the Lewis acidity of B(C6F5)3 is slightly lower than that of BF3 and significantly reduced compared to BCl3. B(C6F5)3 forms a strong Lewis adduct with water, which was shown to be a strong Brønsted acid having an acidity comparable to hydrochloric acid (in acetonitrile). In consequence, even traces of moisture are able to deactivate B(C6F5)3 and remaining catalytic activity might only be due to the Brønsted acidity of the water adduct.

Applications in catalysis
In one application (C6F5)3B forms noncoordinating anions by removing anionic ligands from metal centers. Illustrative is a reaction that give rise to alkene polymerization catalysts where tris(pentafluorophenyl)boron is used as an activator or cocatalyst:
 * (C6F5)3B + (C5H5)2Zr(CH3)2 → [(C5H5)2ZrCH3]^{+}[(C6F5)3BCH3](−)

In this process, the strongly coordinating methyl group transfers to the boron to expose a reactive site on zirconium. The resulting cationic zirconocene species is stabilised by the non coordinating borane anion. The exposed site on the zirconium allows for coordination of alkenes, whereupon migratory insertion into the remaining carbon-methyl ligand gives rise to a propyl ligand this process continues resulting in the growth of a polymer chain. This reagent has led to the development of immobilised catalyst/activator species; where the catalyst/activator is immobilised on an inert inorganic support such as silica.

is also capable of abstracting hydride to give [(C6F5)3BH](−), and it catalyzes hydrosilylation of aldehydes. Otherwise (C6F5)3B binds to a wide range of Lewis bases, even weak ones. The compound is hygroscopic, forming the trihydrate [(C6F5)3BOH2](H2O)2, wherein one water in coordinated to boron and the other two waters are hydrogen-bonded to the coordinated water.

Related compounds are halides.

Frustrated Lewis pair
Tris(pentafluorophenyl)borane is a key reagent leading to the concept of frustrated Lewis pairs. The combination of BCF and bulky basic phosphines, such as tricyclohexylphosphine (PCy3) cleaves H2:
 * (C6F5)3B + PCy3 + H2 → (C6F5)3BH(−) + HPCy3^{+}

Many related phosphines, boranes, and substrates participate in related reactions.

Other reactions
(C6F5)3B was used to prepare a compound containing a Xe-C bond:
 * (C6F5)3B + XeF2 → [C6F5Xe]^{+}[(C6F5)2BF2](−)

Upon reaction with, the salt of the noncoordinating anion lithium tetrakis(pentafluorophenyl)borate is formed.
 * (C6F5)3B + C6F5Li → Li[(C6F5)4B]

B(C6F5)3 reacts with to give the zwitterionic phosphonic-boronate (mes = C6H2Me3):
 * (C6F5)3B + mes2PH → (C6F5)2B(F)\sC6F4\sP(H)mes2

This zwitterionic salt can be converted to a system that reversibly binds molecular H2:
 * (C6F5)2B(F)\sC6F4\sP(H)mes2 + Me2SiHCl → (C6F5)2B(H)\sC6F4\sP(H)mes2 + Me2SiFCl
 * (C6F5)2B(H)\sC6F4\sP(H)mes2 → (C6F5)2B\sC6F4\sPmes2 + H2