Core-Modified meso-Aryl Hexaphyrins with an Internal Thiophene Bridge: Structure, Aromaticity, and Photodynamics

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DC Field	Value	Language
dc.contributor.author	Karthik, Ganesan	-
dc.contributor.author	Sneha, Mahima	-
dc.contributor.author	Raja, V. Prabhu	-
dc.contributor.author	Srinivasan, A.	-
dc.contributor.author	Chandrashekar, Tavarekere K.	-
dc.date.accessioned	2024-12-12T12:13:02Z	-
dc.date.available	2024-12-12T12:13:02Z	-
dc.date.issued	2013-01-04	-
dc.identifier.citation	Karthik, G., Sneha, M., Raja, V. P., Lim, J. M., Kim, D., Srinivasan, A., & Chandrashekar, T. K. (2013). Core-modified meso-aryl hexaphyrins with an internal thiophene bridge: structure, aromaticity, and photodynamics. Chemistry (Weinheim an Der Bergstrasse, Germany), 19(6), 1886–1890.	en_US
dc.identifier.uri	https://doi.org/10.1002/chem.201203737	-
dc.identifier.uri	http://idr.niser.ac.in:8080/jspui/handle/123456789/1145	-
dc.description.abstract	The synthesis of core-modified meso aryl hexaphyrins with an internal thiophene bridge is reported. Introduction of the thiophene bridge alters the electronic structure as well as the π-electron circuit, resulting in increases in singlet lifetime (τs) and the two-photon absorption (TPA) cross-section. Furthermore, for the sulfur derivative, the internal bridging thiophene participates in a π-electron conjugation pathway.	en_US
dc.language.iso	en	en_US
dc.publisher	Chemistry - A European Journal	en_US
dc.title	Core-Modified meso-Aryl Hexaphyrins with an Internal Thiophene Bridge: Structure, Aromaticity, and Photodynamics	en_US
dc.type	Article	en_US
Appears in Collections:	Journal Papers

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