Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule
Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule
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Date
2013-02-21
Authors
Elumalai, Palani
Rajakannu, Palanisamy
Hussain, Firasat
Sathiyendiran, Malaichamy
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Abstract
Arranging an aromatic cyclic trimer into a tripodal molecule was achieved by the reaction of tri(bromomethyl)benzene with substituted benzimidazoles. The edge-to-face C-H⋯π interactions in the trimer stabilize the conformation of flexible molecules. © 2013 The Royal Society of Chemistry.
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RSC Advances. v.3(7)