Chiral smectic C phases exhibited by biphenyl resorcylate and vanillate derivatives

Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/2891

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DC Field	Value	Language
dc.contributor.author	Jeon, Y.J.	-
dc.contributor.author	Lee, J.C.	-
dc.contributor.author	Shivkumar, B.	-
dc.date.accessioned	2007-06-15T07:16:17Z	-
dc.date.available	2007-06-15T07:16:17Z	-
dc.date.issued	1999-01	-
dc.identifier.citation	Liquid Crystals, 1999, Vol.26, p1129 - 1133	en
dc.identifier.issn	0267-8292	-
dc.identifier.issn	1366-5855 (Online)	-
dc.identifier.uri	http://hdl.handle.net/2289/2891	-
dc.description	Restricted Access.	en
dc.description.abstract	We report the synthesis and mesomorphic behaviour of alkoxybiphenyl resorcylate and vanillate derivatives with a chiral moiety obtained from chloro analogues of L-leucine, L-valine and L-isoleucine. The compounds have been characterized by NMR spectroscopy and the mesophases studied by DSC and optical microscopy. In the synthesized compounds, an enantiotropic chiral smectic C phase over a wide temperature range has been observed. Changes in the phase behaviour caused by structural variations in the core and the optically active alkyl chain are also discussed.	en
dc.format.extent	168885 bytes	-
dc.format.mimetype	application/pdf	-
dc.language.iso	en	en
dc.publisher	Taylor & Francis	en
dc.relation.uri	http://dx.doi.org/10.1080/026782999204156	en
dc.rights	1999 Taylor & Francis	en
dc.title	Chiral smectic C phases exhibited by biphenyl resorcylate and vanillate derivatives	en
dc.type	Article	en
Appears in Collections:	Research Papers (SCM)

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