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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dc.contributor.author Uzun, Duygu
dc.contributor.author Özser, Mustafa E.
dc.contributor.author Yüney, Kıvanç
dc.contributor.author Icil, Huriye
dc.contributor.author Demuth, Martin
dc.date.accessioned 2017-10-23T08:42:42Z
dc.date.available 2017-10-23T08:42:42Z
dc.date.issued 2003
dc.identifier.issn 1873-2666(online)
dc.identifier.issn 1010-6030(print)
dc.identifier.uri http://dx.doi.org/10.1016/S1010-6030(02)00436-7
dc.identifier.uri http://hdl.handle.net/11129/3465
dc.description Due to copyright restrictions, the access to the publisher version (published version) of this article is only available via subscription. You may click URI and have access to the Publisher Version of this article through the publisher web site or online databases, if your Library or institution has subscription to the related journal or publication. en_US
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-perylenebis(dicarboximide) (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. en_US
dc.language.iso eng en_US
dc.publisher Elsevier B.V en_US
dc.relation.isversionof 10.1016/S1010-6030(02)00436-7 en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject N, N′-Bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide), N, N′-Bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide, en_US
dc.subject Aggregation, Organic solar cells, Electron transfer reactions, en_US
dc.subject N,N′-Bis(4-cyanophenyl)-3,4,9,10-perylenebis(dicarboximide), N,N′-Bis(4-cyanophenyl)-1,4,5,8-naphthalenediimide, en_US
dc.subject PERYLENE, SOLAR-CELLS, DERIVATIVES, CHEMISTRY, PHYSICAL, en_US
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 en_US
dc.type letter en_US
dc.relation.journal Journal of Photochemistry & Photobiology, A: Chemistry en_US
dc.contributor.department Eastern Mediterranean University, Faculty of Arts & Sciences, Department of Chemstiry en_US
dc.identifier.volume 156 en_US
dc.identifier.issue 1 en_US
dc.identifier.startpage 45 en_US
dc.identifier.endpage 54 en_US


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