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

Title: Chiral smectic C phases exhibited by biphenyl resorcylate and vanillate derivatives
Authors: Jeon, Y.J.
Lee, J.C.
Shivkumar, B.
Issue Date: Jan-1999
Publisher: Taylor & Francis
Citation: Liquid Crystals, 1999, Vol.26, p1129 - 1133
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.
Description: Restricted Access.
URI: http://hdl.handle.net/2289/2891
ISSN: 0267-8292
1366-5855 (Online)
Alternative Location: http://dx.doi.org/10.1080/026782999204156
Copyright: 1999 Taylor & Francis
Appears in Collections:Research Papers (SCM)

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