Please use this identifier to cite or link to this item: http://idr.niser.ac.in:8080/jspui/handle/123456789/1145
Title: Core-Modified meso-Aryl Hexaphyrins with an Internal Thiophene Bridge: Structure, Aromaticity, and Photodynamics
Authors: Karthik, Ganesan
Sneha, Mahima
Raja, V. Prabhu
Srinivasan, A.
Chandrashekar, Tavarekere K.
Issue Date: 4-Jan-2013
Publisher: Chemistry - A European Journal
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.
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.
URI: https://doi.org/10.1002/chem.201203737
http://idr.niser.ac.in:8080/jspui/handle/123456789/1145
Appears in Collections:Journal Papers

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