NMR-SPECTROSCOPY OF ORGANOLITHIUM COMPOUNDS .16. THE AGGREGATION BEHAVIOR OF BUTYLLITHIUM, PHENYLLITHIUM, AND LITHIUM DIISOPROPYLAMIDE IN DIMETHOXYMETHANE AND DIETHOXYMETHANE
K. Bergander et al., NMR-SPECTROSCOPY OF ORGANOLITHIUM COMPOUNDS .16. THE AGGREGATION BEHAVIOR OF BUTYLLITHIUM, PHENYLLITHIUM, AND LITHIUM DIISOPROPYLAMIDE IN DIMETHOXYMETHANE AND DIETHOXYMETHANE, Tetrahedron, 50(20), 1994, pp. 5861-5868
The aggregation behaviour of butyllithium (BuLi), phenyllithium (PhLi)
, and lithium diisopropylamide (LDA) in dimethoxy- and diethoxymethane
(methylal and ethylal, respectively) has been studied by NMR spectros
copy using the isotopic fingerprint method and C-13,Li-6 as well as N-
15,Li-6 spin-spin coupling constants. In both solvents, LDA exists as
a dimer. while BuLi forms a tetramer. PhLi forms a dimer in methylal,
whereas two major aggregates exist in ethylal. Due to solvent viscosit
y at lower temperatures, their structure could not be determined.