Iron(II) tetrafluoroborate

Iron(II) tetrafluoroborate
Names
	IUPAC name Iron(II) tetrafluoroborate
	Other names Ferrous tetrafluoroborate;
Identifiers
CAS Number	(anhydrous): 15283-51-9;
3D model (JSmol)	(anhydrous): Interactive image;
ChemSpider	(anhydrous): 9911059;
ECHA InfoCard	100.035.736
EC Number	(anhydrous): 239-327-0;
PubChem CID	(anhydrous): 11736352; (hexahydrate): 15762351;
CompTox Dashboard (EPA)	(anhydrous): DTXSID30884830 ;
	InChI InChI=1S/2BF4.Fe/c22-1(3,4)5;/q2-1;+2 Key: GXZXLFFLHJJJLX-UHFFFAOYSA-N;
	SMILES (anhydrous): [B-](F)(F)(F)F.[B-](F)(F)(F)F.[Fe+2];
Properties
Chemical formula	Fe(BF4)2
Molar mass	229.46 g/mol (anhydrous); 337.55 g/mol (hexahydrate)
Appearance	Light green crystals; (hexahydrate)
Solubility in water	Soluble
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H312, H314, H332
Precautionary statements	P260, P261, P264, P270, P271, P280, P301+P312, P301+P330+P331, P302+P352, P303+P361+P353, P304+P312, P304+P340, P305+P351+P338, P310, P312, P321, P322, P330, P363, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references

Iron(II) tetrafluoroborate or ferrous tetrafluoroborate is an inorganic chemical with chemical formula Fe(BF₄)₂. Both the anhydrous form and a hexahydrate are known. The hexahydrate and aqueous solutions are green. Tetrafluoroborate is generally a weakly coordinating anion, so iron(II) tetrafluoroborate is used as the starting material for forming various other iron(II) coordination complexes.

For example, a complex composed of iron(II) tetrafluoroborate and the ligand tris[2-(diphenylphosphino)-ethyl]phosphine catalyzes the transfer hydrogenation of various aldehydes to give the corresponding primary alcohols, using formic acid as hydrogen donor.^[1]

References

^ Gerrit Wienhöfer; Felix A.Westerhaus; Kathrin Junge; Matthias Beller (2013). "Fast and selective iron-catalyzed transfer hydrogenations of aldehydes". Journal of Organometallic Chemistry. 744: 156–159. doi:10.1016/j.jorganchem.2013.06.010.

[iron-catalyst-1] Gerrit Wienhöfer; Felix A.Westerhaus; Kathrin Junge; Matthias Beller (2013). "Fast and selective iron-catalyzed transfer hydrogenations of aldehydes". Journal of Organometallic Chemistry. 744: 156–159. doi:10.1016/j.jorganchem.2013.06.010.

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