Chemistry:Organovanadium chemistry

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Organovanadium chemistry is the chemistry of organometallic compounds containing a carbon (C) to vanadium (V) chemical bond.[1] Organovanadium compounds find only minor use as reagents in organic synthesis but are significant for polymer chemistry as catalysts.[2]

Oxidation states for vanadium are +2, +3, +4 and +5. Low valency vanadium is usually stabilized with carbonyl ligands. Oxo derivatives are relatively common, unlike the organic complexes of neighboring elements.

Compound classes

Carbonyls

Vanadium carbonyl can be prepared by reductive carbonylation of vanadium salts:

4 Na + VCl3 + 6 CO → Na[V(CO)6] + 3 NaCl

The salt can be oxidized to the 17e binary carbonyl V(CO)6.

Cyclopentadienyl derivatives

thumb|right|130px|(Cycloheptatrienyl)(cyclopentadienyl)vanadium is one of many organovanadium compounds that is paramagnetic. Vanadocene dichloride, the first organovanadium complexes to be reported,[3] is prepared from sodium cyclopentadienyl and vanadium tetrachloride:

2 NaC5H5 + VCl4 → VCp2Cl2 + 2NaCl

Reduction of this compound gives the parent vanadocene (Cp2V):

VCp2Cl2 + LiAlH4 → VCp2
Cp2V2(CO)5 featuring a pair of semi-bridging CO ligands.[4]

Vanadocene is the lightest transition metal metallocene that is isolable at room temperature.[5] Vanadocene reacts with high pressures of carbon monoxide to give CpV(CO)4.[6] Photolysis of the tetracarbonyl gives Cp2V2(CO)5. Several analogous indenyl complexes are known.

Monocyclopentadienyl vanadium chlorides include CpVCl3 and the diamagnetic CpVOCl2.

Arene complexes

Vanadium forms a variety of arene complexes, e.g. with benzene:

VCl4 + Al + 2 C6H6 → [V(η6-C6H6)2]AlCl4
[V(η6-C6H6)2]AlCl4 + H2O → V(η6-C6H6)2 + ...

Alkyl and aryl derivatives

A handful of alkyl and aryl complexes exist. The reactive species V(mesityl)3 forms from VCl3:[7]

VCl3(THF)3 + 3 LiC6H2-2,4,6-Me3 → V(C6H2-2,4,6-Me3)3(THF) + 3 LiCl

This species binds CO and, under appropriate conditions, N2. V(mesityl)3 adds a fourth mesityl group and the resulting "ate complex" can be oxidized to the vanadium(IV) derivative:

V(mes)3(THF) + LiMes → Li[V(mes)4]
Li[V(mes)4] + air → V(mes)4(THF)

The tetrakis(norbornyl) complex is also known.

Vanadium oxytrichloride is a starting material for organovanadium(IV) and organovanadium(V) compounds:

VOCl3 + Li(mes) → Li[VO(mes)3]
Li[VO(mes)3] + chloranil → VO(mes)3
VOCl3 + ZnPh2 → VOPhCl2 + "ZnPh(Cl)"

Catalysts and reagents

Well-defined vanadium compounds do not appear as catalysts in any commercial process.[8] However organovanadium species are clearly implicated as catalysts for the production of butadiene-based rubbers. These catalysts are generated in situ by treating soluble coordination complexes such as vanadium(III) acetylacetonate with organoaluminium activators.[9][10]

References

  1. ↑ Synthesis of Organometallic Compounds: A Practical Guide Sanshiro Komiya Ed. 1997
  2. ↑ Kotohiro Nomura; Shu Zhang (2011). "Design of Vanadium Complex Catalysts for Precise Olefin Polymerization". Chem. Rev. 111 (3): 2342–2362. doi:10.1021/cr100207h. PMID 21033737. 
  3. ↑ Wilkinson, G.; Birmingham, J. G. (1954). "Bis-cyclopentadienyl Compounds of Ti, Zr, V, Nb and Ta". Journal of the American Chemical Society 76 (17): 4281–4284. doi:10.1021/ja01646a008. 
  4. ↑ Fischer, Ernst Otto; Schneider, Robert J. J. (1970). "Über Aromatenkomplexe von Metallen, CXIV. Darstellung und Reaktionen von Dicyclopentadienyl‐divanadin‐pentacarbonyl, (C 5 H 5 ) 2 V 2 (CO) 5". Chemische Berichte 103 (11): 3684–3695. doi:10.1002/cber.19701031133. 
  5. ↑ Robert Choukroun, Christian Lorber (2005). "Adventures in Vanadocene Chemistry". Eur. J. Inorg. Chem. 2005 (23): 4683–4692. doi:10.1002/ejic.200500371. 
  6. ↑ King, R.B.; Stone, F.G.A (1963). "Cyclopentadienyl Metal Carbonyls and Some Derivatives". Inorganic Syntheses. 7. 99–115. doi:10.1002/9780470132388.ch31. ISBN 978-0-470-13238-8. 
  7. ↑ Vivanco, M.; Ruiz, J.; Floriani, C.; Chiesi-Villa, A.; Rizzoli, C. "Chemistry of the vanadium-carbon .sigma. bond. 1. Insertion of carbon monoxide, isocyanides, carbon dioxide, and heterocumulenes into the V-C bond of Tris(mesityl)vanadium(III)" Organometallics 1993 volume 12, 1794–1801. doi:10.1021/om00029a042
  8. ↑ Toshikazu Hirao (1997). "Vanadium in Modern Organic Synthesis". Chemical Reviews 97 (8): 2707–2724. doi:10.1021/cr960014g. PMID 11851478. 
  9. ↑ Kotohiro Nomura; Shu Zhang (2011). "Design of Vanadium Complex Catalysts for Precise Olefin Polymerization". Chem. Rev. 111 (3): 2342–2362. doi:10.1021/cr100207h. PMID 21033737. 
  10. ↑ Werner Obrecht; Jean-Pierre Lambert; Michael Happ; Christiane Oppenheimer-Stix; John Dunn; Ralf Krüger (2012). "Ullmann's Encyclopedia of Industrial Chemistry". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.o23_o01. 



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