Issue 7, 2013

Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule

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.

Graphical abstract: Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule

Supplementary files

Article information

Article type
Communication
Submitted
29 Oct 2012
Accepted
07 Dec 2012
First published
11 Dec 2012

RSC Adv., 2013,3, 2171-2173

Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule

P. Elumalai, P. Rajakannu, F. Hussain and M. Sathiyendiran, RSC Adv., 2013, 3, 2171 DOI: 10.1039/C2RA22679K

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