A new type of alkylamines possessing high nitrogen inversion-rotation (NIR)
barriers is described (in general, these are hindered cyclic amines). The
increase in barrier values for these amines is caused by an increase in ste
ric interactions in the NIR transition state due to restrictions for N-subs
tituent rotation (usually steric repulsion of N-substituents is decreased o
n going to a planar NIR transition state of alkylamines). Since these compo
unds may be essentially different in structure, a comparison between the NI
R barriers of homologs is proposed as a criterion for the assignment of ami
nes to this type. According to this criterion, the NIR barriers are drastic
ally increased (3-5 kcal mol(-1)) on going from NMe or NH (usual amines) to
more bulky N-alkylhomologs (amines of the third type). Structures of some
of these amines were predicted and their NIR barriers were estimated by MM3
. Copyright (C) 1999 John Wiley & Sons, Ltd.