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Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/4251
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dc.contributor.authorSaha, H.K.-
dc.contributor.authorMallick, D.-
dc.contributor.authorDas, S.-
dc.date.accessioned2022-11-25T07:32:15Z-
dc.date.available2022-11-25T07:32:15Z-
dc.date.issued2022-11-25-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/4251-
dc.description.abstractLinear and curved antiaromatic s-indacenodicarbazole isomers were synthesized and characterized to show the tunable paratropicity of s-indacene, as analyzed by NICS(1)zz and ACID (ring-current) calculations. The curved isomer showed a greater degree of antiaromaticity than the linear isomer, as predicted by the Glidewell-Lloyd rule. This degree of antiaromaticity was further validated by the red-shifted UV-vis absorption and smaller HOMO-LUMO energy gap.en_US
dc.language.isoen_USen_US
dc.titleUnveiling two antiaromatic s-indacenodicarbazole isomers with tunable paratropicityen_US
dc.typeArticleen_US
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