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The structure of the tetrafluoroborate anion, BF

Tetrafluoroborate is the anion BF
. This tetrahedral species is isoelectronic with tetrafluoromethane, CF4 and tetrafluoroammonium NF+
, and is valence isoelectronic with many stable and important species including the perchlorate anion, ClO
, which is used in similar ways in the laboratory. It arises by the reaction of fluoride salts with the Lewis acid BF3, treatment of tetrafluoroboric acid with base, or by treatment of boric acid with hydrofluoric acid.

As an anion in inorganic and organic chemistry[edit]

The popularization of BF
has led to decreased use of ClO
in the laboratory. With organic compounds, especially amine derivatives, ClO
forms potentially explosive derivatives. One disadvantage to BF
is its slight sensitivity to hydrolysis, whereas ClO
does not suffer from this problem. Safety considerations, however, overshadow this inconvenience.

The utility of BF
arises because its salts are often more soluble in organic solvents than the related nitrate or halide salts. Furthermore, BF
is less nucleophilic and basic than nitrates and halides. Thus, when using salts of BF
, one can usually assume that the cation is the reactive agent and this tetrahedral anion is inert. BF
owes its inertness to two factors: (i) it is symmetrical so that the negative charge is distributed equally over several (four) atoms, and (ii) it is composed of highly electronegative fluorine atoms, which diminish the basicity of the anion. Related to BF
is hexafluorophosphate, PF
, which is even more stable toward hydrolysis and whose salts tend to be more lipophilic.

Illustrative of a fluoroborate salt is [Ni(CH3CH2OH)6](BF4)2, a kinetically labile octahedral complex, which is used as a source of Ni2+.[1]

Extremely reactive cations such as those derived from Ti, Zr, Hf, and Si do in fact abstract fluoride from BF
, so in such cases BF
is not an "innocent" anion and less coordinating anions must be employed. Moreover, in other cases of ostensibly "cationic" complexes, the fluorine atom acts as a bridging ligand between boron and the cationic center. For instance, the gold complex [μ-(DTBM-SEGPHOS)(Au–BF4)2] was found crystallographically to contain two Au–F–B bridges.[2]

Transition and heavy metal fluoroborates are produced in the same manner as other fluoroborate salts; the respective metal salts are added to reacted boric and hydrofluoric acids. Tin, lead, copper, and nickel fluoroborates are prepared through electrolysis of these metals in a solution containing HBF4.

Examples of salts[edit]

Potassium fluoroborate is obtained by treating potassium carbonate with boric acid and hydrofluoric acid.

B(OH)3 + 4 HF → HBF4 + 3 H2O
2 HBF4 + K2CO3 → 2 KBF4 + H2CO3

Fluoroborates of alkali metals and ammonium ions crystallize as water-soluble hydrates with the exception of potassium, rubidium, and caesium.

Fluoroborate salts are often associated with highly reactive compounds. Some examples include

See also[edit]


  1. ^ Willem L. Driessen, Jan Reedijk (1992). "Solid Solvates: The Use of Weak Ligands in Coordination Chemistry". Inorganic Syntheses. Inorganic Syntheses. 29: 111–118. doi:10.1002/9780470132609.ch27. ISBN 978-0-470-13260-9.
  2. ^ Abadie, Marc-Antoine; Trivelli, Xavier; Medina, Florian; Capet, Frédéric; Roussel, Pascal; Agbossou-Niedercorn, Francine; Michon, Christophe (2014-08-01). "Asymmetric Intramolecular Hydroamination of Alkenes in Mild and Wet Conditions—Structure and Reactivity of Cationic Binuclear Gold(I) Catalysts". ChemCatChem. 6 (8): 2235–2239. doi:10.1002/cctc.201402350. ISSN 1867-3899.