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Please use this identifier to cite or link to this item: https://idr.l1.nitk.ac.in/jspui/handle/123456789/8354
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dc.contributor.authorAlla, R.A.-
dc.contributor.authorHegde, G.-
dc.contributor.authorIsloor, A.M.-
dc.contributor.authorChandrakantha, B.-
dc.contributor.authorShetty, P.-
dc.contributor.authorKomitov, L.-
dc.date.accessioned2020-03-30T10:18:29Z-
dc.date.available2020-03-30T10:18:29Z-
dc.date.issued2010-
dc.identifier.citationIDW'10 - Proceedings of the 17th International Display Workshops, 2010, Vol.1, , pp.81-83en_US
dc.identifier.urihttp://idr.nitk.ac.in/jspui/handle/123456789/8354-
dc.description.abstractA new series of 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy moiety were synthesized by refluxing mixture of acid hydrazide 3 with different aromatic carboxylic acid in phosphorous oxychloride. Photoalignment studies were performed on these materials indicating that the position of fluorine plays vital role in promoting planar alignment either parallel or perpendicular to the light polarization direction. � 2010 ITE and SID.en_US
dc.titleInvestigation of the photoalignment effect of 1, 3, 4-oxadiazoles bearing 2-fluoro-4-methoxy phenyl moietyen_US
dc.typeBook chapteren_US
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