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Stabilization of Metal Alkoxides (M = BA, CU) by Alkamolamines

Published online by Cambridge University Press:  25 February 2011

L. G. Hubert-Pfalzgraf
Affiliation:
laboratoire de Chimie Moléculaire, URA CNRS, Université de Nice-Sophia Antipolis, BP 71, 06108 Nice Cedex 2, France
M. C. Massiani
Affiliation:
laboratoire de Chimie Moléculaire, URA CNRS, Université de Nice-Sophia Antipolis, BP 71, 06108 Nice Cedex 2, France
J. C. Daran
Affiliation:
Laboratoire de Métaux de Transition, URA CNRS, 75230 Paris, France.
J. Vaissermann
Affiliation:
Laboratoire de Métaux de Transition, URA CNRS, 75230 Paris, France.
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Abstract

Alcohol interchange reactions between barium and copper(II) methoxides and triethanolamine give Ba(teaH-l)2,2EtOH and [Cu(teaH-2)]4,3tea, respectively. Triethanolamine appears as a tetradentate ligand -chelating in the case of barium, bridging-chelating for copper - and thus ensures high coordination numbers for the metals - eight for Ba and five for Cu - thus decreasing their susceptibility to hydrolysis. The remaining hydroxyl functionality on the coordinated triethanolamine moities favors the formation of solvates with alcohols via H-bonding.

Type
Research Article
Copyright
Copyright © Materials Research Society 1992

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References

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