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Tetramethylammonium fluoride

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Tetramethylammonium fluoride
Names
IUPAC name
tetramethylazanium;fluoride
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.006.154 Edit this at Wikidata
EC Number
  • 206-769-0
  • InChI=1S/C4H12N.FH/c1-5(2,3)4;/h1-4H3;1H/q+1;/p-1
    Key: GTDKXDWWMOMSFL-UHFFFAOYSA-M
  • C[N+](C)(C)C.[F-]
Properties
C4H12FN
Molar mass 93.145 g·mol−1
Appearance white solid
Hazards
GHS labelling:
GHS07: Exclamation mark
Warning
H302, H312, H315, H319, H332, H335
P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetramethylammonium fluoride is the quaternary ammonium salt with the formula (CH3)4NF. This colorless solid is a source of “naked fluoride", that is fluoride ions not connected to a metal atom in a complex. Most other soluble salts of fluoride are in fact bifluorides, HF2. Tetramethylammonium fluoride is produced by combining tetramethylammonium hydroxide and hydrogen fluoride in isopropanol. Due to the high basicity of the fluoride anion, the salt reacts slowly with acetonitrile, inducing its dimerization to CH3C(NH2)=CHCN, which co-crystallizes.[1]

Related salts

(CH3)3P=CH2 + KHF2 → (CH3)4PF + KF
In the gas phase, tetramethylphosphonium fluoride exists as the phosphorane, but in acetonitrile solution, it dissociates into ions.[2]

References

  1. ^ "Syntheses, Properties, and Structures of Anhydrous Tetramethylammonium Fluoride and Its 1:1 Adduct with trans-3-Amino-2-butenenitrile". Journal of the American Chemical Society. 112: 7619–7625. 1990. doi:10.1021/ja00177a025. {{cite journal}}: Cite uses deprecated parameter |authors= (help)
  2. ^ Kornath, Andreas; Neumann, F.; Oberhammer, H. (2003). "Tetramethylphosphonium Fluoride: "Naked" Fluoride and Phosphorane". Inorganic Chemistry. 42: 2894–2901. doi:10.1021/ic020663c.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  3. ^ Schwesinger, Reinhard (2001). "1,1,1,3,3,3-Hexakis(dimethylamino)-1λ5,3λ5-diphosphazenium Fluoride". e-EROS Encyclopedia of Reagents for Organic Synthesis. pp. 1–2. doi:10.1002/047084289X.rh014m.
  4. ^ Haoran Sun; Stephen G. DiMagno (2005). "Anhydrous Tetrabutylammonium Fluoride". Journal of the American Chemical Society. 127 (7): 2050–1. doi:10.1021/ja0440497. PMID 15713075. {{cite journal}}: Unknown parameter |lastauthoramp= ignored (|name-list-style= suggested) (help)