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Diboron tetrafluoride

From Wikipedia, the free encyclopedia
Chemical compound
Diboron tetrafluoride
Names Preferred IUPAC name
Diboron tetrafluoride
Systematic IUPAC name
Tetrafluorodiborane(4)
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/B2F4/c3-1(4)2(5)6
    Key: WUWOPJNIAKTBSJ-UHFFFAOYSA-N
  • FB(F)B(F)F
Properties B2F4 Molar mass 97.61 g·mol−1 Appearance Colorless gas Density 4.3 kg/m3 (gas) Melting point −56 °C (−69 °F; 217 K) Boiling point −34 °C (−29 °F; 239 K) Thermochemistry 79.1 J/mol K 317.3 J/mol K -1440.1 kJ/mol -1410.4 kJ/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Diboron tetrafluoride is the inorganic compound with the formula (BF2)2. A colorless gas, the compound has a halflife of days at room temperature. It is the most stable of the diboron tetrahalides,[1] and does not appreciably decompose under standard conditions.[2]

Structure and bonding

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Diboron tetrafluoride is a planar molecule with a B-B bond distance of 172 pm.[1] Although it is electron-deficient, the unsaturated boron centers are stabilized by pi-bonding with the terminal fluoride ligands. The compound is isoelectronic with oxalate.

Synthesis and reactions

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Diboron tetrafluoride can be formed by treating boron monofluoride with boron trifluoride at low temperatures, taking care not to form higher polymers.[3] Alternatively, diboron tetrachloride can be fluorinated with antimony trifluoride.[2]

Addition of diboron tetrafluoride to Vaska's complex was employed to produce an early example of a transition metal boryl complex:[4]

2 B2F4 + IrCl(CO)(PPh3)2 → Ir(BF2)3(CO)(PPh3)2 + ClBF2

Historical literature

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References

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  1. ^ a b Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  2. ^ a b Arthur Finch and Hermann Irving Schlesinger (1958). "Diboron Tetrafluoride". J. Am. Chem. Soc. 80 (14): 3573–3574. doi:10.1021/ja01547a020.
  3. ^ Timms, P. L. (1972). "Low Temperature Condensation of High Temperature Species as a Synthetic Method" . Advances in Inorganic Chemistry and Radiochemistry. Academic Press: 143. doi:10.1016/S0065-2792(08)60006-0. ISBN 0-12-023614-1.
  4. ^ Neeve, Emily C.; Geier, Stephen J.; Mkhalid, Ibraheem A. I.; Westcott, Stephen A.; Marder, Todd B. (2016). "Diboron(4) Compounds: From Structural Curiosity to Synthetic Workhorse". Chemical Reviews. 116 (16): 9091–9161. doi:10.1021/acs.chemrev.6b00193 . hdl:1807/78811 . PMID 27434758.


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Salts and covalent derivatives of the fluoride ion
HF ?HeF2
FrF RaF2   LrF3 Rf Db Sg Bh Hs Mt Ds Rg Cn Nh Fl Mc Lv Ts Og
PF6, AsF6, SbF6 compounds
AlF2−5, AlF3−6 compounds
chlorides, bromides, iodides
and pseudohalogenides
SiF2−6, GeF2−6 compounds
Oxyfluorides
Organofluorides
with transition metal,
lanthanide, actinide, ammonium
nitric acids
bifluorides
thionyl, phosphoryl,
and iodosyl

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