Synthesis and photophysical properties of <i>N</i>,<i>N</i>′-bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide) and <i>N</i>,<i>N</i>′-bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide
JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, vol.156, no.1-3, pp.45-54, 2003 (SCI-Expanded, Scopus)
- Publication Type: Article / Article
- Volume: 156 Issue: 1-3
- Publication Date: 2003
- Doi Number: 10.1016/s1010-6030(02)00436-7
- Journal Name: JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY
- Journal Indexes: Science Citation Index Expanded (SCI-EXPANDED), Scopus
- Page Numbers: pp.45-54
- Middle East Technical University Northern Cyprus Campus Affiliated: No
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.