Vanadyl isopropoxide

Vanadyl isopropoxide
Names
	Other names Triisopropoxyvanadium(V) oxide; VTIP; Vanadium(V) trisisopropoxide oxide
Identifiers
CAS Number	5588-84-1;
3D model (JSmol)	Interactive image;
ChemSpider	21171176;
ECHA InfoCard	100.024.544
EC Number	226-997-4;
PubChem CID	79702;
CompTox Dashboard (EPA)	DTXSID60904393;
	InChI InChI=1S/3C3H8O.O.V/c31-3(2)4;;/h33-4H,1-2H3;; Key: JOUSPCDMLWUHSO-UHFFFAOYSA-N;
	SMILES CC(C)O.CC(C)O.CC(C)O.O=[V];
Properties
Chemical formula	C9H21O4V
Molar mass	244.205 g·mol−1
Melting point	−14 to −11 °C (7 to 12 °F; 259 to 262 K)
Boiling point	242 °C (468 °F; 515 K)
Hazards
GHS pictograms
GHS Signal word	Warning
GHS hazard statements	H226, H315, H319, H335
GHS precautionary statements	P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+352, P303+361+353, P304+340, P305+351+338, P312, P321, P332+313, P337+313, P362, P370+378, P403+233, P403+235, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
	Infobox references

Vanadyl isopropoxide is the metal alkoxide with the formula VO(O-iPr)₃ (iPr = CH(CH₃)₂). A yellow volatile liquid, it is a common alkoxide of vanadium. It is used as a reagent and as a precursor to vanadium oxides.[1] The compound is diamagnetic. It is prepared by alcoholysis of vanadyl trichloride:

VOCl₃ + 3 HOCH(CH₃)₂ → VO(OCH(CH₃)₂)₃ + 3 HCl

The related cyclopentanoxide VO(O-CH(CH₂)₄)₃ is a dimer, one pair of alkoxide ligands bind weakly trans to the vanadyl oxygens.[2]

References

Krumeich, F.; Muhr, H.-J.; Niederberger, M.; Bieri, F.; Schnyder, B.; Nesper, R. (1999). "Morphology and Topochemical Reactions of Novel Vanadium Oxide Nanotubes". Journal of the American Chemical Society. 121 (36): 8324–8331. doi:10.1021/ja991085a.
Hillerns, Frank; Olbrich, Falk; Behrens, Ulrich; Rehder, Dieter (1992). "Tris(cyclopentanolato)oxovanadium(V): A Model for the Transition State of Enzymatic Phosphoester Cleavage". Angewandte Chemie International Edition in English. 31 (4): 447–448. doi:10.1002/anie.199204471.

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[1] Krumeich, F.; Muhr, H.-J.; Niederberger, M.; Bieri, F.; Schnyder, B.; Nesper, R. (1999). "Morphology and Topochemical Reactions of Novel Vanadium Oxide Nanotubes". Journal of the American Chemical Society. 121 (36): 8324–8331. doi:10.1021/ja991085a.

[2] Hillerns, Frank; Olbrich, Falk; Behrens, Ulrich; Rehder, Dieter (1992). "Tris(cyclopentanolato)oxovanadium(V): A Model for the Transition State of Enzymatic Phosphoester Cleavage". Angewandte Chemie International Edition in English. 31 (4): 447–448. doi:10.1002/anie.199204471.