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Reversible redox switching between local and global aromaticity for core-modified expanded carbaisophlorinoids

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dc.contributor.author AMBHORE, MADAN D. en_US
dc.contributor.author PANCHAL, SANTOSH P. en_US
dc.contributor.author Mondal, Arpan en_US
dc.contributor.author Konar, Sanjit en_US
dc.contributor.author ANAND, V. G. en_US
dc.date.accessioned 2022-04-22T08:11:56Z
dc.date.available 2022-04-22T08:11:56Z
dc.date.issued 2022-03 en_US
dc.identifier.citation Organic & Biomolecular Chemistry en_US
dc.identifier.issn 1477-0520 en_US
dc.identifier.issn 1477-0539 en_US
dc.identifier.uri https://doi.org/10.1039/D1OB02230J en_US
dc.identifier.uri http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6745
dc.description.abstract Two dithienothiophene based 28π antiaromatic macrocycles with benzene and azulene units and their effects on local and global (anti)aromaticity have been described. Experimental and computational studies confirmed the presence of weak paratropic and strong diatropic ring current effects in neutral and dicationic states, respectively. en_US
dc.language.iso en en_US
dc.publisher Royal Society of Chemistry en_US
dc.subject Porphyrin en_US
dc.subject States en_US
dc.subject 2022-APR-WEEK1 en_US
dc.subject TOC-APR-2022 en_US
dc.subject 2022 en_US
dc.title Reversible redox switching between local and global aromaticity for core-modified expanded carbaisophlorinoids en_US
dc.type Article en_US
dc.contributor.department Dept. of Chemistry en_US
dc.identifier.sourcetitle Organic & Biomolecular Chemistry. en_US
dc.publication.originofpublisher Foreign en_US


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