Fluorescent macromolecular perylene diimides containing pyrene or indole units in bay positions

dc.contributor.authorDinçalp, H
dc.contributor.authorKizilok, S
dc.contributor.authorIçli, S
dc.date.accessioned2025-04-10T10:32:25Z
dc.date.available2025-04-10T10:32:25Z
dc.description.abstractNovel, symmetric and unsymmetric perylene diimide dyes with pyrene or indole units in the bay positions of the perylene ring were synthesized and characterized using FT-IR, H-1 and C-13 NMR, MS, UV-Vis spectra and cyclic voltammetry. The lambda(max) different solvents were in the range 526-585 nm and emission wavelengths of the dyes exhibited positive solvatochromism with increasing solvent polarity. Long wavelength emissions >750 nm of dyes with pyrene units displayed charge-separated state of perylene-pyrene system. Dyes with pyrene or indole units showed greater photostability in toluene than dyes which did not contain these bulky substituents. Incorporating electron-donating indole substituents lowered the band gap energies and, therefore, the HOMO energy levels were increased. The energy density and shape of the molecular orbitals were calculated theoretically. (C) 2009 Elsevier Ltd. All rights reserved.
dc.identifier.e-issn1873-3743
dc.identifier.issn0143-7208
dc.identifier.urihttp://hdl.handle.net/20.500.14701/38830
dc.language.isoEnglish
dc.titleFluorescent macromolecular perylene diimides containing pyrene or indole units in bay positions
dc.typeArticle

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