Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/3005
Full metadata record
DC FieldValueLanguage
dc.contributor.authorPal, S.K.-
dc.date.accessioned2020-12-11T05:21:10Z-
dc.date.available2020-12-11T05:21:10Z-
dc.date.issued2013-
dc.identifier.citationLiquid Crystals, 40(2), pp.281-292.en_US
dc.identifier.otherhttps://doi.org/10.1080/02678292.2012.747112-
dc.identifier.urihttps://www.tandfonline.com/doi/full/10.1080/02678292.2012.747112-
dc.identifier.urihttp://hdl.handle.net/123456789/3005-
dc.descriptionOnly IISERM authors are available in the record.-
dc.description.abstractMicrowave-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_US
dc.language.isoenen_US
dc.publisherTaylor & Francisen_US
dc.subjectLiquid crystalsen_US
dc.subjectRufigallolen_US
dc.subjectOligomeren_US
dc.subjectCyanobiphenylen_US
dc.titleSynthesis and characterisation of novel alkoxycyanobiphenyl-substituted rufigallolsen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

Files in This Item:
File Description SizeFormat 
Need to add pdf.odt8.63 kBOpenDocument TextView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.