Cc. Chang et al., CARBODIIMIDE INSERTION INTO ORGANOALUMINUM COMPOUNDS AND THERMAL REARRANGEMENT OF THE PRODUCTS, Organometallics, 17(8), 1998, pp. 1595-1601
A series of carbodiimide insertion products were prepared using variou
s aluminum reagents (viz., AlR3 (R = Me, Et), AlX2Y (X = Cl, R; Y = Cl
, NR2')) and 1,3-diisopropyl- and 1,3-di-tert-butylcarbodiimides in va
rious stoichiometric ratios. The resulting products 1-20 were isolated
either as colorless liquids or as solids. These compounds were charac
terized by H-1 NMR, C-13 NMR, IR, and mass spectral data. Elemental an
alysis data for some of the representative compounds were obtained. Th
e crystal structures of two of the compounds (compounds 8 '' and 10) w
ere determined by single-crystal X-ray diffraction. The competitive mi
gration of the alkyl, chloro, or amino group attached to the aluminum
atom onto the carbon of the carbodiimide is also reported.