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.
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.
|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|
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