Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule
Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule
| dc.contributor.author | Elumalai, Palani | |
| dc.contributor.author | Rajakannu, Palanisamy | |
| dc.contributor.author | Hussain, Firasat | |
| dc.contributor.author | Sathiyendiran, Malaichamy | |
| dc.date.accessioned | 2022-03-27T08:36:00Z | |
| dc.date.available | 2022-03-27T08:36:00Z | |
| dc.date.issued | 2013-02-21 | |
| dc.description.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. | |
| dc.identifier.citation | RSC Advances. v.3(7) | |
| dc.identifier.uri | 10.1039/c2ra22679k | |
| dc.identifier.uri | http://xlink.rsc.org/?DOI=c2ra22679k | |
| dc.identifier.uri | https://dspace.uohyd.ac.in/handle/1/11131 | |
| dc.title | Design strategy for arranging an aromatic cyclic trimer into a tripodal molecule | |
| dc.type | Journal. Article | |
| dspace.entity.type |
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