Please use this identifier to cite or link to this item: http://dspace.iitrpr.ac.in:8080/xmlui/handle/123456789/4251
Title: Unveiling two antiaromatic s-indacenodicarbazole isomers with tunable paratropicity
Authors: Saha, H.K.
Mallick, D.
Das, S.
Issue Date: 25-Nov-2022
Abstract: Linear 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.
URI: http://localhost:8080/xmlui/handle/123456789/4251
Appears in Collections:Year-2022

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