Crystal structures of n-BuLi adducts with (R,R)-TMCDA and the consequences for the deprotonation of benzene.

Combinations of organolithium compounds and diamine bases have become a powerful tool in synthetic chemistry. Because of the structure-reactivity relationship, the elucidation of reaction mechanisms of these reagents is strongly connected with the structural determination of intermediate species. In mixtures of the diamine TMCDA (N,N,N',N'-tetramethylcyclohexane-1,2-diamine) and n-butyllithium, two different structures, the dimeric [n-BuLi x (R,R)-TMCDA]2 and the aggregate [(n-BuLi)2 x (R,R)-TMCDA]2, can be isolated, depending on the n-BuLi/TMCDA ratio. Thereby, [(n-BuLi)2 x (R,R)-TMCDA]2 is a rare example of an organolithium compound with a ladder arrangement of the central four-membered Li-C-Li-C rings. Two isomers of the ladder structure are formed in the crystal by changing from the enantiomerically pure to racemic TMCDA. As n-BuLi/TMCDA mixtures are also able to deprotonate benzene, these structures give hint to possible mechanisms. Supported by theoretical studies, transition states based on the dimer, the ladder structure, and a hypothetical monomer are discussed.