Planar hexaphyrin-like macrocycles turning into bis-BODIPYs with box-shaped structures exhibiting excitonic coupling

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/4828

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DC Field	Value	Language
dc.contributor.author	Dhamija, Shaina	-
dc.contributor.author	De, Arijit K.	-
dc.date.accessioned	2023-08-18T09:56:41Z	-
dc.date.available	2023-08-18T09:56:41Z	-
dc.date.issued	2021	-
dc.identifier.citation	Chemical Communications, 57(87), 11485–11488.	en_US
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2021/CC/D1CC04403F	-
dc.identifier.uri	http://hdl.handle.net/123456789/4828	-
dc.description	Only IISERM authors are available in the record	en_US
dc.description.abstract	Planar carbazole based hexaphyrin-like macrocycles with biscoordinating cores and box-shaped cyclic BODIPYs were synthesized. Solution and solid-state structure analysis of the free macrocycles indicates an inversion of two pyrrole rings, resulting in a two-dipyrrinlike environment. The BF2 complexes show large Stokes shifts and exhibit excitonic coupling, fine-tuned by the meso-substituents.	en_US
dc.language.iso	en_US	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	macrocycles	en_US
dc.subject	box-shaped	en_US
dc.title	Planar hexaphyrin-like macrocycles turning into bis-BODIPYs with box-shaped structures exhibiting excitonic coupling	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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