100098-22-4Relevant articles and documents
The out,out to out,in transition for 1,(n+2)-diazabicyclo[n.3.1]alkanes
Alder, Roger W.,Heilbronner, Edgar,Honegger, Evi,McEwen, Alan B.,Moss, Richard E.,Olefirowicz, Edward,Petillo, Peter A.,Sessions, Richard B.,Weisman, Gary R.,White, Jonathan M.,Yang, Zhong-Zhi
, p. 6580 - 6591 (1993)
Hexahydropyrimidines N,N-bridged by a chain of n methylene groups (1,(n+2)-diazabicyclo[n.3.1]alkanes) adopt out,out (axial,axial) structures for n=2,3 , and 4. When n=5, the photoelectron spectrum shows evidence of the presence of some of the out,in (axial,equatorial) isomer in the gas phase, although none can be found in solution. When n=6, the compound is apparently entirely out,in in the gas phase but exists as a mixture of out,out and out,in confonners in solution. For n=7, only the diamond lattice out,in isomer can be detected in solution. These experimental data are correlated with force field (MM2) calculations; multiple minimum search methods have been used to locate all low-energy conformations. Semiempirical calculations (MNDO, AM1, and PM3) have been carried out on model systems. Related tricyclic bis-aminals having 10- and 12-membered rings have also been studied. They adopt [2323] and [3333] conformations, respectively, each having out,in (equatorial,axial) bridged hexahydropyrimidine rings. For several of the compounds, dynamic NMR processes are observed, and possible mechanisms for these are discussed.
