Hexacatenars Exhibiting π-π Driven Supergelation, Aggregation Induced Blue Light Emission and Thermochromism

dc.contributor.authorGupta, Monika
dc.contributor.authorPal, S.K.
dc.date.accessioned2020-12-03T06:50:47Z
dc.date.available2020-12-03T06:50:47Z
dc.date.issued2016
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstractTwo series of five ring polycatenars, which vary from each other with respect to the position of connection to the central benzene ring are reported. The overall shape of the molecule plays a major role than the number of flexible tails in the periphery in dictating the self‐assembly (liquid crystallinity and gelation) and the photophysical behavior. Tetracatenars were crystalline and meta‐substituted compounds exhibited reduced tendency to stabilize the mesophase. In the para‐substituted series, all the hexacatenars exhibited columar hexagonal phase. p‐Substituted hexacatenar with n‐dodecyloxy tails exhibited thermochromism, with the highly emissive Colh phase and non‐emissive soft crystal phase. Three p‐substituted compounds exhibited supergelation exclusively promoted by π‐π interactions. Besides the capability to form self‐standing, moldable gel, one of the compounds exhibited technologically important aggregation‐induced blue light emission. The columnar order and emissive nature in the aggregated state makes these molecules promising for the application in emissive displays.en_US
dc.identifier.citationChemistrySelect, 1(16), pp. 5107-5120en_US
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/abs/10.1002/slct.201600927
dc.language.isoenen_US
dc.publisherWiley-Blackwellen_US
dc.subjectPolycatenarsen_US
dc.subjectSupergelationen_US
dc.subjectThermochromismen_US
dc.subjectBlue Light Emissionen_US
dc.titleHexacatenars Exhibiting π-π Driven Supergelation, Aggregation Induced Blue Light Emission and Thermochromismen_US
dc.typeArticleen_US

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