Santos-Perez, J. and Crespo-Hernandez, C. E. and Reichardt, C. and Cabrera, C. R. and Feliciano-Ramos, I. and Arroyo-Ramirez, L. and Meador, M. A.. (2011) Synthesis, Optical Characterization, and Electrochemical Properties of Isomeric Tetraphenylbenzodifurans Containing Electron Acceptor Groups. Journal of Physical Chemistry A, 115 (17). pp. 4157-4168.
Full text not available from this repository.Abstract
Isomeric tetraphenylbenzodifuran systems, benzo-[1,2-b:5,4]difuran and benzo[1,2-b:4,5]difuran, containing electron acceptor groups (CF(3), CN, and NO(2)) have been synthesized and studied. Their electronic absorption, fluorescence, two-photon absorption cross sections, and electrochemical properties were investigated. The absorption and emission maxima are red-shifted for the linear-conjugated systems in comparison with the corresponding isomer. Dual fluorescence was observed and the existence of a twisted intramolecular charge transfer state was confirmed by low-temperature emission experiments. Wide HOMO-LUMO energy gaps were obtained ranging from 2.53 to 3.28 eV. HOMO levels were found in the energy range of -6.03 to -6.63 eV while LUMO are within -2.55 to -3.52 eV.
Item Type: | Article |
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InterNano Taxonomy: | Nanomanufacturing Characterization Techniques |
Collections: | Nanomanufacturing Research Collection > Nanomanufacturing Nanoscale Science and Engineering Centers > Center for Hierarchical Manufacturing |
Depositing User: | Robert Stevens |
Date Deposited: | 03 May 2012 17:01 |
Last Modified: | 03 May 2012 17:01 |
URI: | http://eprints.internano.org/id/eprint/1783 |
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