The relative stability of classical versus nonclassical mono- and bis-boron
analogs of the 2-norbornyl cation was investigated by ab initio and densit
y functional methods. Nonclassical structures were preferred in carbon brid
ged isoelectronic 1,2-diboranorbornyl anions having the following substitue
nts on boron: H, CH3 and CN. The difluoro analog preferred the classical st
ructure. The mono-boron analog preferred an open structure. (C) 2001 Elsevi
er Science Ltd. All rights reserved.