A third type of alkylamines possessing high nitrogen inversion-rotation barriers

Citation
Am. Belostotskii et A. Hassner, A third type of alkylamines possessing high nitrogen inversion-rotation barriers, J PHYS ORG, 12(8), 1999, pp. 659-663
Citations number
26
Categorie Soggetti
Organic Chemistry/Polymer Science
Journal title
JOURNAL OF PHYSICAL ORGANIC CHEMISTRY
ISSN journal
08943230 → ACNP
Volume
12
Issue
8
Year of publication
1999
Pages
659 - 663
Database
ISI
SICI code
0894-3230(199908)12:8<659:ATTOAP>2.0.ZU;2-U
Abstract
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.