The reaction of 1,2,4,5‐(Me2NCH2)4C6H2 with one equivalent of n‐butyllithium affords Li2[C6H(CH2NMe2)4‐2,3,5,6]2 (1). The molecule consists of a dimeric unit containing three‐centre, two‐electron lithium‐bonded aryl groups. The distorted tetrahedral coordination sphere of the lithium atoms is completed by two N‐coordinating ortho‐CH2NMe2 substituents. Complex 1 is the first dimeric aryllithium compound characterized in which the coordination around lithium is completed solely by intramolecular donating hetero atoms.
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ZEIJDEN et al. (1988) studied this question.
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