Hostname: page-component-586b7cd67f-t7czq Total loading time: 0 Render date: 2024-11-25T15:26:25.026Z Has data issue: false hasContentIssue false

Tailored Molecular Precursors of Yttrium Oxide Using Functional Alcohols and Acetylacetone as Modifiers

Published online by Cambridge University Press:  28 February 2011

Liliane G. Hubert-Pfalzgraf
Affiliation:
Laboratoire de Chimie Moléculaire, Associé au CNRS, Université de Nice-Sophia Antipolis, Parc Valrose, 06034 Nice, France
Olivier Poncelet
Affiliation:
Laboratoire de Chimie Moléculaire, Associé au CNRS, Université de Nice-Sophia Antipolis, Parc Valrose, 06034 Nice, France
Jean-Claude Daran
Affiliation:
Laboratoire de Chimie des Métaux de Transition, Place Jussieu, 75230 Paris, France
Get access

Abstract

Yttrium is involved as oxide in a variety of advanced materials. Hydrolysis of its most common alkoxide, yttrium oxoisopropoxide Y5O(OiPr)13 , is difficult to control as a result of the high electropositivity of the metal. Functional alcohols such as 2-methoxyethanol and acetylacetone have thus been used as modifiers. These tailored precursors have been fully characterized (single crystal X-Ray diffraction, IR, NMR. ). The tendency of methoxyethanol to act as a bridging ligand and to stabilize high oligomers - Y(OC2H4OMe)3 is a decamer - gives some insight into its behavior as “network builder”. The unexpected cleavage of acetylacetone offers a route to an interesting acetatoacetylacetonate derivative, Y2(OAc)2(acac)4(H2O)2 , but also suggest that this classical “modifier” could be affected by the hydrolysis-polycondensation reactions of the metallic species during the sol-gel process. Comparison of the hydrolysis behavior of the different precursors was performed.

Type
Research Article
Copyright
Copyright © Materials Research Society 1990

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Ulrich, D.R., Chem. Eng. News, 1990, 28. ;Google Scholar
1a. Sanders, H.J., ibid, 1984, 26.Google Scholar
2. Yamashita, K., Nojimi, T., Umegaki, T. and Kamazawa, T., Solid State Ionics 35, 299 (1989).Google Scholar
3. Hubert-Pfalzgraf, L.G., New J. Chem. 11, 663 (1987).Google Scholar
4. Poncelet, O., Sartain, W.J., Hubert-Pfalzgraf, L.G., Folting, K. and Caulton, K.G., Inorg. Chem. 28, 263 (1989).Google Scholar
5. Brown, L.M. and Mazdiasni, K.S., Inorg. Chem. 9, 783 (1970).Google Scholar
6. x = 1, m = 4 in the case of neodymium, as established by X-ray diffraction studies.Google Scholar
7. Livage, J., Henry, M. and Sanchez, C., Progress in Solid State Chem. 18, 259 (1988).Google Scholar
8. Poncelet, O., Hubert-Pfalzgraf, L.G. and Daran, J.C., J. Chem. Soc. Chem. Commun. 1989, 1846.Google Scholar
9. Poncelet, O., Hubert-Pfalzgraf, L.G. and Daran, J.C., Polyhedron, in the press.Google Scholar
9a. Poncelet, O., Hubert-Pfalzgraf, L.G. and Daran, J.C., Inorg. Chem., in the press.Google Scholar
10. Leaustic, A., Babonneau, F. and Livage, J., Chem. of Mater. 1, 240, 248 (1989).Google Scholar
11. Nanao, T. and Eguchi, T., Patent EP 84/104 194 840413, CA 102 ,099 762.Google Scholar
12. Goel, S.C., Kramer, K.S., Gibbon, P.C. and Buhro, W.E., Inorg. Chem. 28. 3619 (1989).Google Scholar
13. El Khokh, N., Papiernik, R., Hubert-Pfalzgraf, L.G., Chaput, F. and Boilot, J.P., J. Mater. Sci. Lett. 8, 762 (1989).Google Scholar
14. Sanchez, C., Livage, J., Henry, M. and Babonneau, F., J. Non-Cryst. Solids 100, 65, (1988).Google Scholar