The reactions of trimethylgallium and trimethylindium with a variety o
f secondary amines [HNMe(2), HNEt(2), HNPr2n, HNPr2i, HNBu(2)(n), HNBu
(2)(i), HNBu(2)(s), HN(CH(2)Ph)(2), HN(c-C6H11)(2), HNC4HB8 HNC5H10, H
NC6H12 and HN(CH(2)CH2)(2)NMe], produce a series of room-temperature s
table liquid or solid adducts. These were characterized by H-1 and C-1
3 NMR, IR, mass spectrometry and elemental analysis. Spectroscopic com
parisons are made between these and the corresponding trimethylaluminu
m derivatives. H-1 and C-13 NMR data for all three series of adducts i
ndicate a correlation between the chemical shifts of the methyl groups
on the metal and the relative steric requirements of the amines. The
data show a general downfield movement of these chemical shifts with i
ncreasing steric bulk.