Sodium tetraphenylborate
Names
Preferred IUPAC name
Sodium tetraphenylboranuide
Other names
Tetraphenylboron sodium
Kalignost
Identifiers
3D model (JSmol)
ECHA InfoCard 100.005.096
UNII
  • InChI=1S/C24H20B.Na/c1-5-13-21(14-6-1)25(22-15-7-2-8-16-22,23-17-9-3-10-18-23)24-19-11-4-12-20-24;/h1-20H;/q-1;+1
  • [B-](C1=CC=CC=C1)(C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4.[Na+]
Properties
(C6H5)4BNa
Molar mass 342.216 g/mol
Appearance white solid
Melting point > 310 °C (590 °F; 583 K)
47 g/100 mL
Solubility soluble in ethanol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Infobox references

Sodium tetraphenylborate is the organic compound with the formula NaB(C6H5)4. It is a salt, wherein the anion consists of four phenyl rings bonded to boron. This white crystalline solid is used to prepare other tetraphenylborate salts, which are often highly soluble in organic solvents. The compound is used in inorganic and organometallic chemistry as a precipitating agent for potassium, ammonium, rubidium, and cesium ions, and some organic nitrogen compounds.

Synthesis and structure

Sodium tetraphenylborate is synthesized by the reaction between sodium tetrafluoroborate and phenylmagnesium bromide:

NaBF4 + 4 PhMgBr → 2 MgBr2 + 2 MgF2 + NaBPh4 (where Ph = phenyl)

A related synthesis involves the use of phenylsodium in place of the Grignard reagent.[1]

Unlike smaller counteranions, such as nitrate and the halides, tetraphenylborate confers lipophilicity to its salts. Many analogous tetraarylborates have been synthesized, containing both electron-rich and electron-deficient aryl groups.

The anhydrous salt adopts a polymeric structure in the solid state consisting of Na+-phenyl interactions. As such the salt could be classified as an organosodium compound.[2]

Use in chemical synthesis

Preparation of N-acylammonium salts

Addition of sodium tetraphenylborate to a solution of a tertiary amine and an acid chloride in acetonitrile gives the acylonium salt by precipitating NaCl from the reaction mixture. This method has a broad scope:[3]

RC(O)Cl + R'3N + NaB(C6H5)4 → [RC(O)NR'3][B(C6H5)4] + NaCl

Sodium tetraphenylborate is also employed as a phenyl donor in palladium-catalyzed cross-coupling reactions involving vinyl and aryl triflates to give arylalkenes and biaryl compounds in good yields and under mild conditions, respectively.[4]

Use in coordination chemistry

Tetraphenylborates are often studied in organometallic chemistry because of their good solubility in nonpolar solvents and their crystallinity. For example, the homoleptic trimethylphosphite complexes {M[P(OCH3)3]5}2+ (Ni, Pd, and Pt) have been prepared as their tetraphenylborate salts.[5] Similarly, sodium tetraphenylborate has been used to isolate complexes containing dinitrogen ligands.[6] In the reaction below, sodium tetraphenylborate allows N2 to displace the chloride ligand, which is removed from solution as a precipitate of sodium chloride:

FeHCl(diphosphine)2 + NaB(C6H5)4 + N2 → [FeH(N2)(diphosphine)2]B(C6H5)4 + NaCl

The use of tetraphenylborate is limited to non-acidic cations. With strong acids, the anion undergoes protonolysis to give triphenylborane and benzene:[7]

H+ + B(C6H5)4− → B(C6H5)3 + C6H6

Weakly coordinating anions often are based on tetraarylborates, with electronegative substituents. Examples include B(C6F5)4− and Brookhart's acid containing the tetrakis[3,5-bis(trifluoromethyl)phenyl]borate anion.

References

  1. ↑ R. M. Washburn, F. A. Billig, "Tetraarylboron Compounds"US Patent 3,311,662.
  2. ↑ Ulrich Behrens, Frank Hoffmann, and Falk Olbrich "Solid-State Structures of Base-Free Lithium and Sodium Tetraphenylborates at Room and Low Temperature: Comparison with the Higher Homologues MB(C6H5)4 (M = K, Rb, Cs)" Organometallics 2012, volume 31, p. 905−913. doi:10.1021/om200943n
  3. ↑ J. King & G. Bryant (1992). "Preparation and characterization of crystalline N-acylammonium salts". J. Org. Chem. 57 (19): 5136. doi:10.1021/jo00045a025.
  4. ↑ P. Ciattini; E. Morera; G. Ortar (1992). "Palladium-catalyzed cross-coupling reactions of vinyl and aryl triflates with tetraarylborates". Tetrahedron Letters. 33 (33): 4815. doi:10.1016/S0040-4039(00)61293-5.
  5. ↑ J. P. Jesson, M. Cushing, S. D. Ittel (2007). "Pentakis(Trimethyl Phosphite) Complexes of the D8 Transition Metals". Pentakis(Trimethylphosphite) Complexes of the d8 Transition Metals. Inorganic Syntheses. Vol. 20. pp. 76–82. doi:10.1002/9780470132517.ch22. ISBN 9780470132517.{{cite book}}: CS1 maint: multiple names: authors list (link)
  6. ↑ M. Mays & E. Prater (1974). "trans ‐(dinitrogen)bis[ethylenebis‐(diethylphosphine)]hydridoiron(II) Tetraphenylborate". Inorganic Syntheses. Vol. 15. pp. 21–25. doi:10.1002/9780470132463.ch6. ISBN 9780470132463. {{cite book}}: |journal= ignored (help)
  7. ↑ Tianshu Li, Alan J. Lough, Cristiano Zuccaccia, Alceo Macchioni, and Robert H. Morris "An acidity scale of phosphonium tetraphenylborate salts and ruthenium dihydrogen complexes in dichloromethane" Can. J. Chem. 84(2): 164–175 (2006). doi:10.1139/V05-236.
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.