Synthesis and mesomorphic properties of unsymmetrical bent-core compounds containing 1,3-phenylene or 2,7-naphthylene as the central unit

Shreenivasa Murthy, H.N.; Sadashiva, B.K.

Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/2907

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DC Field	Value	Language
dc.contributor.author	Shreenivasa Murthy, H.N.	-
dc.contributor.author	Sadashiva, B.K.	-
dc.date.accessioned	2007-06-18T04:14:16Z	-
dc.date.available	2007-06-18T04:14:16Z	-
dc.date.issued	2004-10	-
dc.identifier.citation	Liquid Crystals, 2004, Vol.31, p1347 - 1356	en
dc.identifier.issn	0267-8292	-
dc.identifier.issn	1366-5855 (Online)	-
dc.identifier.uri	http://hdl.handle.net/2289/2907	-
dc.description	Restricted Access.	en
dc.description.abstract	The synthesis and mesomorphic properties of four new homologous series of unsymmetrical bent-core compounds with 1,3-phenylene or 2,7-naphthylene as the central unit are reported. These compounds contain an agr-methylcinnamoyloxy bridging group in one of the arms. Three types of mesophases, namely, N, B1 and B2 are observed in these compounds. The rarely observed transitions N to B1 and N to B2 have been observed in some of the compounds derived from 2,7-dihydroxynaphthalene. In one of the compounds derived from resorcinol, textural features of both B1 and B2 phases appear simultaneously on cooling the isotropic phase. The mesophases were characterized using conventional techniques.	en
dc.format.extent	404290 bytes	-
dc.format.mimetype	application/pdf	-
dc.language.iso	en	en
dc.publisher	Taylor & Francis	en
dc.relation.uri	http://dx.doi.org/10.1080/02678290412331286024	en
dc.rights	2004 Taylor & Francis	en
dc.title	Synthesis and mesomorphic properties of unsymmetrical bent-core compounds containing 1,3-phenylene or 2,7-naphthylene as the central unit	en
dc.type	Article	en
Appears in Collections:	Research Papers (SCM)

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