Niobium(V) ethoxide is an metalorganic compound with formula Nb2(OC2H5)10. It is a colorless liquid that dissolves in some organic solvents but hydrolyzes readily.[2] It is mainly used for the sol-gel processing of materials containing niobium oxides.[4]
10.svg) Skeletal structure of niobium(V) ethoxide
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| Identifiers | |
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3D model (JSmol)
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| ChemSpider | |
| ECHA InfoCard | 100.019.814 |
| EC Number |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C10H25NbO5 | |
| Molar mass | 318.209 g mol−1 |
| Appearance | Colourless liquid |
| Density | 1.258 g cm−3 |
| Melting point | 5 °C (41 °F; 278 K) |
| Boiling point | 203 °C (397 °F; 476 K) |
| N/A; reacts with water[2] | |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
−1583.9 ± 2.7 kJ mol−1[3] |
Std enthalpy of
combustion (ΔcH⦵298) |
−6872.6 ± 1.7 kJ mol−1[3] |
| Hazards | |
| GHS labelling: | |
 
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| Danger | |
| H226, H314 | |
| P210, P233, P240, P241, P242, P243, P260, P264, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P370+P378, P403+P235, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 36 °C; 97 °F; 309 K |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Structure
editMetal alkoxides rarely adopt monomeric structures, and niobium(V) ethoxide is no exception. Early studies established that niobium alkoxides aggregate in solution as dimers.[5] Subsequent crystallographic analysis established that the methoxide and isopropoxides of niobium adopt bioctahedral structures.[6] From a geometric perspective, the ten ethoxide ligand oxygen atoms of the Nb2(OEt)10 molecule in solution define a pair of octahedra sharing a common edge with the two niobium atoms located at their centres. From a bonding perspective, each niobium centre is surrounded octahedrally by four monodentate and two bridging ethoxide ligands. The oxygen atoms of the bridging ethoxides are each bonded to both niobium centres, and these two ligands are cis to one another within the coordination sphere. The formula [(EtO)4Nb(μ-OEt)]2 more comprehensively represents this dimeric structure, though the simplified formula is commonly used for most purposes.
Preparation and reactions
editThis compound is prepared by salt metathesis from niobium pentachloride (Et = C2H5):
- 10 NaOEt + Nb2Cl10 → Nb2(OC2H5)10 + 10 NaCl
The most important reaction of niobium alkoxides is their hydrolysis to produce films and gels of niobium oxides.[4] Although these reactions are complex, they can be described by this simplified equation:
- Nb2(OC2H5)10 + 5 H2O → Nb2O5 + 10 HOEt
The thermal decomposition of Nb(OC2H5)5 begins above 325 – 350 °C. This can be observed with QMS as an increasing amount of ethanol and ethane released. Diethyl ether, C2H5OC2H5, and niobium(V) oxide are the decomposition products released following an atomic layer deposition or chemical vapor deposition process. The decomposition reaction can be summarised as:[7]
- Nb2(OC2H5)10 → Nb2O5 + 5 O(C2H5)2
References
edit- ^ "ChemSpider CSID:13600". ChemSpider. Retrieved 17 November 2012.
- ^ a b W. M. Haynes. CRC Handbook of Chemistry and Physics, 93rd Edition. Physical Constants of Inorganic Compounds.
- ^ a b "Niobium(5+) ethanolate". webbook.nist.gov. Retrieved November 15, 2012.
- ^ a b U. Schubert "Sol–Gel Processing of Metal Compounds" Comprehensive Coordination Chemistry II 2003, Pages 629–656 Volume 7. doi:10.1016/B0-08-043748-6/06213-7
- ^ Bradley, D. C.; Holloway, C. E. (1968). "Nuclear Magnetic Resonance Studies on Niobium and Tantalum Penta-alkoxides". J. Chem. Soc. A: 219–223. doi:10.1039/J19680000219. S2CID 98638647.
- ^ Mehrotra, Ram C.; Singh, Anirudh (1997). "Recent Trends in Metal Alkoxide Chemistry". In Karlin, Kenneth D. (ed.). Progress in Inorganic Chemistry. Vol. 46. John Wiley & Sons. pp. 239–454. doi:10.1002/9780470166475.ch4. ISBN 9780470167045.
- ^ Rahtu, Antti (2002). Atomic Layer Deposition of High Permittivity Oxides: Film Growth and In Situ Studies (Thesis). University of Helsinki. hdl:10138/21065. ISBN 952-10-0646-3.