Alkylaluminoxane compositions and their preparation

Organic compounds -- part of the class 532-570 series – Organic compounds – Aluminum containing

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556179, 556180, 502103, 502117, 502152, 526160, 526943, C07F 506, C07F 1700

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060138203

ABSTRACT:
The reaction between an alkylaluminum compound such as trimethylaluminum and carbon dioxide or an organic carbonyl reagent such as benzoic acid or benzophenone is facilitated and accelerated by contacting these reactants in the presence of an inert organic solvent/diluent and a catalytic quantity of water. The process is preferably conducted using continuous feeds of the components to the reaction zone. The proportions of (I) and (ii) fed to the reactor are maintained such that there are about 1.4 to about 2.2 moles of alkylaluminum per mole of oxygen atoms as CO.sub.2 or the organic carbonyl reagent, and the weight ratio of aluminum alkyl to the solvent/diluent is preferably in the range ca. 20:80 to ca. 60:40. Polyalkylaluminoxanes formed in the process can have better solubility in paraffinic or cycloparaffinic hydrocarbons, and also greater storage stability.

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patent: 5728855 (1998-03-01), Smith et al.
Eisch, John J., "Aluminum" Chapter 10, Comprehensive Organometallic Chemistry II, vol. 1, 1995, pp. 431-502.
Mole, et al., "Exhaustive C-Methylation of Carboxylic Acids by Trimethylaluminum: A New Route to t-Butyl Compounds", Aust. J. Chem., 1974, vol. 27, pp. 1665-1672.
Mole, et al., "Exhaustive C-Methylation of Ketones by Trimethylaluminum", Aust. J. Chem., 1974, vol. 27, pp. 1655-1663.
Mole, et al., "C-Methylation of Alcohols by Trimethylaluminum", Aust. J. Chem., 1974, vol. 27, pp. 1639-1653.
Mole, et al., "Hemi-Alkoxides From Reactions of Trimethylaluminum With Aldehydes or Ketones", Aust. J. Chem., 1970, vol. 23, pp. 715-724.

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