1972Journal of the Chemical Society Faraday Transactions 1 Physical Chemistry in Condensed PhasesRequires access

Reactions of group 3 metal alkyls in the gas phase. Part 9.—Addition of propene to trimethylaluminium

Kurt W. Egger

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Abstract

The thermal gas phase reaction of propene with monomeric trimethylaluminium has been studied at temperatures from 455 to 549 K using a static reaction system and Teflon coated reaction vessels. Initial propene pressures ranged from 190 to 370 Torr (25.33 to 49.33 kN m–2) and the ratio of propene to AlMe3 varied from 4.9 to 24.1. Overall conversions between 0.4 and 12.4 % with respect to alkyl groups were observed. In excess propene the overall reaction involves the rate determining addition of propene to the Al—CH3 bond (k1) to give Me2AlBui followed by the fast elimination of isobutene and subsequent addition of propene to Me2AlH, yielding Me2AlPrn.The rate constant k1, corrected for path degeneracy, is given (with standard errors) by the Arrhenius relationship log(k1/l. mol–1 s–1)= 5.60 ± 0.18 –(20.35 ± 0.44)/θ where θ= 2.303 RT/kcal mol–1.These results when compared with earlier data for the systems AlEt3+ ethylene and AlMe3+ ethylene appear to support a one-step 4-centre concerted process rather than the concept of olefinaluminium alkyl complexes as intermediates formed in these reactions, as proposed earlier.

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The thermal gas phase reaction of propene with monomeric trimethylaluminium has been studied at temperatures from 455 to 549 K using a static reaction system and Teflon coated reaction vessels. Initial propene pressures ranged from 190 to 370 Torr (25.33 to 49.33 kN m–2) and the ratio of propene to AlMe3 varied from 4.9 to 24.1. Overall conversions between 0.4 and 12.4 % with respect to alkyl groups were observed. In excess propene the overall reaction involves the rate determining addition of propene to the Al—CH3 bond (k1) to give Me2AlBui followed by the fast elimination of isobutene and subsequent addition of propene to Me2AlH, yielding Me2AlPrn.The rate constant k1, corrected for path degeneracy, is given (with standard errors) by the Arrhenius relationship log(k1/l. mol–1 s–1)= 5.60 ± 0.18 –(20.35 ± 0.44)/θ where θ= 2.303 RT/kcal mol–1.These results when compared with earlier data for the systems AlEt3+ ethylene and AlMe3+ ethylene appear to support a one-step 4-centre concerted process rather than the concept of olefinaluminium alkyl complexes as intermediates formed in these reactions, as proposed earlier.

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Available abstract

The thermal gas phase reaction of propene with monomeric trimethylaluminium has been studied at temperatures from 455 to 549 K using a static reaction system and Teflon coated reaction vessels. Initial propene pressures ranged from 190 to 370 Torr (25.33 to 49.33 kN m–2) and the ratio of propene to AlMe3 varied from 4.9 to 24.1. Overall conversions between 0.4 and 12.4 % with respect to alkyl groups were observed. In excess propene the overall reaction involves the rate determining addition of propene to the Al—CH3 bond (k1) to give Me2AlBui followed by the fast elimination of isobutene and subsequent addition of propene to Me2AlH, yielding Me2AlPrn.The rate constant k1, corrected for path degeneracy, is given (with standard errors) by the Arrhenius relationship log(k1/l. mol–1 s–1)= 5.60 ± 0.18 –(20.35 ± 0.44)/θ where θ= 2.303 RT/kcal mol–1.These results when compared with earlier data for the systems AlEt3+ ethylene and AlMe3+ ethylene appear to support a one-step 4-centre concerted process rather than the concept of olefinaluminium alkyl complexes as intermediates formed in these reactions, as proposed earlier.

Key concepts: Propene, Chemistry, Alkyl, Gas phase, Torr, Metal, Monomer, Reaction rate

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