Synthesis and photophysical properties of N,N?-bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide) and N,N?-bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide

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Elsevier Science Sa

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info:eu-repo/semantics/openAccess

Abstract

N,N'-Bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide (CN-NDI) and N,N'-bis(4-cyanophenyl)-3,4,9,10-peryienebis(dicarboxiniide) (CN-PDI) have been synthesized under special conditions in high yield. The compounds are characterized by UV-Vis, IR, NMR, MS, DSC, TGA and CV measurements. The fluorescence lifetimes, quantum yields and singlet-state energies are presented. CN groups at the phenyl moieties improve the thermal stability of the compounds. The LUMO energy values, -3.91 eV (CN-NDI in solution) and -3.96 eV (CN-NDI and CN-PDI at solid state), are determined by cyclic voltammetry. Whereas CN-NDI shows two reversible (-0.89 and -1.34 V) reduction steps (vs. Fc) in solution, CN-NDI and CN-PDI exhibit only one reversible wave at -0.48 V vs. Ag/AgCl at solid state, assigned to the one-electron reduction. Formation of aggregates shifts the UV absorption spectrum of CN-PDI to shorter wavelengths and its lifetime is measured as 4.6 ns at 580 nm. CN-PDI may be a promising dye for organic solar cells. (C) 2003 Elsevier Science B.V. All rights reserved.

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N,N '-bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide), N,N '-bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide, aggregation, electron transfer reactions, organic solar cells

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Journal of Photochemistry and Photobiology A-Chemistry

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156

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1-3

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