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  • Activation of alkynes by an α-diimine-stabilized Al-Al-bonded compound: insertion into the Al-Al bond or cycloaddition to AlN2C2 rings.

Activation of alkynes by an α-diimine-stabilized Al-Al-bonded compound: insertion into the Al-Al bond or cycloaddition to AlN2C2 rings.

Chemical communications (Cambridge, England) (2013-04-09)
Yanxia Zhao, Yanyan Liu, Yibo Lei, Biao Wu, Xiao-Juan Yang
RESUMO

The reaction of dialumane, [L(2-)(THF)Al(II)-Al(II)(THF)L(2-)] (1, L = [(2,6-iPr2C6H3)NC(Me)]2), with the less reactive diphenylacetylene affords a new insertion product [L(2-)(THF)Al(III)(PhC=CPh)(2-)Al(III)(THF)L(2-)] (2). Reaction of 1 with phenylacetylene (or 4-ethynyltoluene), however, proceeds through cycloaddition of alkynes to the AlN2C2 rings to produce bis(bicyclic) products (3a and 3b).

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Sigma-Aldrich
4-Ethynyltoluene, 97%