Synthesis and characterisation of novel alkoxycyanobiphenyl-substituted rufigallols

Please use this identifier to cite or link to this item: http://hdl.handle.net/2289/5590

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DC Field	Value	Language
dc.contributor.author	Pal, Santanu Kumar	-
dc.contributor.author	Kumar, Sandeep	-
dc.date.accessioned	2013-06-04T06:42:32Z	-
dc.date.available	2013-06-04T06:42:32Z	-
dc.date.issued	2013-02	-
dc.identifier.citation	Liquid Crystals, 2013, Vol. 40, p281-292	en
dc.identifier.issn	0267-8292	-
dc.identifier.issn	1366-5855 (Online)	-
dc.identifier.uri	http://hdl.handle.net/2289/5590	-
dc.description	Restricted Access.	en
dc.description.abstract	Microwave-assisted synthesis of novel alkoxycyanobiphenyl-substituted rufigallols are reported by systematically replacing one, two, four, five or six cyanobiphenyl-tethered alkoxy chains. The synthesis of the target compounds was challenging since classical reactions failed to produce these hybrids. Chemical structures of the hybrids were determined by 1H nuclear magnetic resonance (NMR), 13C NMR, infrared, ultraviolet spectroscopy and elemental analysis. The thermotropic liquid crystalline properties of the new compounds were investigated by polarising optical microscopy, differential scanning calorimetry and X-ray diffractometry	en
dc.language.iso	en	en
dc.publisher	Taylor & Francis	en
dc.relation.uri	http://dx.doi.org/10.1080/02678292.2012.747112	en
dc.rights	2013 Taylor & Francis	en
dc.subject	cyanobiphenyl, oligomer	en
dc.subject	disc–rod hybrids	en
dc.subject	microwave-assisted synthesis	en
dc.title	Synthesis and characterisation of novel alkoxycyanobiphenyl-substituted rufigallols	en
dc.type	Article	en
Appears in Collections:	Research Papers (SCM)

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