Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/5839
Title: Synthesis of Symmetrical and Unsymmetrical Triphenylene Discotic Liquid Crystals Using Antimony(V)Chloride Under Scholl Oxidation
Authors: Kumar, Sandeep
Srinivasa, H.T.
Issue Date: 22-Apr-2013
Publisher: OMICS Group
Citation: Organic Chemistry , 2013, Vol. 2 , p 1000116
Abstract: Triphenylene-based discotic liquid crystals, useful in studying the energy and charge migration in self-organized systems, are the most widely synthesized and studied discotic liquid crystals. In this paper, we report an efficient synthetic procedure for the preparation of symmetrical and unsymmetrical triphenylene discotic liquid crystals using antimony pentachloride as a novel reagent. Scholl oxidative trimarization of 1,2-dialkoxybenzenes with SbCl5 yields hexaalkoxytriphenylenes in good yield, while the oxidative coupling of a 3,3’,4,4’-tetraalkoxybiphenyl with a 1,2,3-trialkoxybenzene affords an unsymmetrically substituted heptaalkoxy-triphenylene derivative. The potential of this new reagent was compared with the other known reagents for the synthesis of alkoxytriphenylenes
Description: Open Access
URI: http://hdl.handle.net/2289/5839
ISSN: 2161-0401
Copyright: Kumar S and Srinivasa HT
Appears in Collections:Research Papers (SCM)

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