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

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