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
| dc.contributor.author | Uzun, D | |
| dc.contributor.author | Ozser, ME | |
| dc.contributor.author | Yuney, K | |
| dc.contributor.author | Icil, H | |
| dc.contributor.author | Demuth, M | |
| dc.date.accessioned | 2026-02-06T18:43:25Z | |
| dc.date.issued | 2003 | |
| dc.department | Doğu Akdeniz Üniversitesi | |
| dc.description.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. | |
| dc.identifier.doi | 10.1016/S1010-6030(02)00436-7 | |
| dc.identifier.endpage | 54 | |
| dc.identifier.issn | 1010-6030 | |
| dc.identifier.issn | 1873-2666 | |
| dc.identifier.issue | 1-3 | |
| dc.identifier.orcid | 0000-0002-3389-6734 | |
| dc.identifier.orcid | 0000-0002-1004-9882 | |
| dc.identifier.orcid | 0000-0001-8189-9123 | |
| dc.identifier.scopus | 2-s2.0-0037456652 | |
| dc.identifier.scopusquality | Q1 | |
| dc.identifier.startpage | 45 | |
| dc.identifier.uri | https://doi.org/10.1016/S1010-6030(02)00436-7 | |
| dc.identifier.uri | https://hdl.handle.net/11129/13583 | |
| dc.identifier.volume | 156 | |
| dc.identifier.wos | WOS:000181809900007 | |
| dc.identifier.wosquality | Q2 | |
| dc.indekslendigikaynak | Web of Science | |
| dc.indekslendigikaynak | Scopus | |
| dc.language.iso | en | |
| dc.publisher | Elsevier Science Sa | |
| dc.relation.ispartof | Journal of Photochemistry and Photobiology A-Chemistry | |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.snmz | KA_WoS_20260204 | |
| dc.subject | N,N '-bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide) | |
| dc.subject | N,N '-bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide | |
| dc.subject | aggregation | |
| dc.subject | electron transfer reactions | |
| dc.subject | organic solar cells | |
| dc.title | 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 | |
| dc.type | Article |










