Gauche and staggered forms of diethylamine in solvates of 1,5-dichloro-cis-9,10-diethynyl-9,10-dihydroanthracene-9,10-diol. A case of conformational pseudopolymorphism?
Raju Mondal,Judith A. K. Howard,Rahul Banerjee,Gautam R. Desiraju
Chemical Communications Pub Date : 02/13/2004 00:00:00 , DOI:10.1039/B316270B
Abstract
Diethylamine has been trapped in its less stable gauche conformation in a solvate of the title diol; the staggered conformation, which is ca. 4 kJ mol−1 more stable, is found in another solvate of the same host.