A new tunable light-emitting and ?-stacked hexa-ethyleneglycol naphthalene-bisimide oligomer: synthesis, photophysics and electrochemical properties

dc.contributor.authorBodapati, Jagadeesh B.
dc.contributor.authorIcil, Huriye
dc.date.accessioned2026-02-06T18:43:39Z
dc.date.issued2011
dc.departmentDoğu Akdeniz Üniversitesi
dc.description.abstractAn oligomer (3) containing flexible hydrophilic hexa(ethylene glycol) and hydrophobic naphthalene-bisimide chromophores has been synthesized by a one-step condensation reaction and its photophysical and electrochemical properties were investigated. 3 was characterized through the data from NMR, IR, UV-vis, GPC, DSC, TGA, elemental analysis and cyclic voltammetry. The average molecular weight (M-w) of 3 was 4430 g mol(-1). Intrinsic viscosity was measured as 0.28 dL g(-1) in m-cresol at 25 degrees C. It has high thermal stability (T-d = 325 degrees C). Interestingly, compound 3 shows excimer-like emission in all kinds of solvents. The band gap energy (E-g), LUMO and HOMO energy values in nonpolar and polar protic solvents were 2.71 eV/3.12 eV, -3.69 eV/-3.88 eV and -6.40 eV/-7.00 eV for 3, respectively. The oligomer showed concentration and solvent dependent fluorescent color tunability. Remarkably, the fluorescent colors of the excimer emissions at 10(-6) M concentration in CHCl3, DMF and MeOH are light yellow, light blue-yellow and strong blue, respectively, and become more intense at higher concentrations. The excimer emission color in CHCl3 and DMF is fluorescent yellow and changed to green in MeOH at 10(-4) M concentration. 3 shows two reversible reduction steps at -1.103 and -1.457 V (vs. ferrocene/ferrocenium) in nonpolar solvent CH2Cl2 and only one at -0.917 V in (50 : 50) CH3OH-CH3CN binary solvent mixture with higher reversibility. Strong blue-shifts of emission band were noted in protic solvents, which confirm the existence of a negative solvatochromism probably due to protonation. The strong solvent-dependent photophysical and electrochemical properties, including the large shift of excimer emission maximum reflecting self-assembly mediated through hydrogen bonding and pi-stacking interactions, make the oligomer a potential candidate for various photo-sensing applications.
dc.description.sponsorshipTurkish Scientific and Technical Research Council (TUBITAK) [110T201]
dc.description.sponsorshipThe authors are thankful to the Turkish Scientific and Technical Research Council (TUBITAK) (Project No: 110T201) for scientific evaluation and monitoring of the project which is financially supported according to the cooperative protocol that is signed between Turkey and North Cyprus. We also thank Dr Peter Montag of the Polymer Standards Service for the GPC measurements.
dc.identifier.doi10.1039/c1pp05019b
dc.identifier.endpage1293
dc.identifier.issn1474-905X
dc.identifier.issn1474-9092
dc.identifier.issue8
dc.identifier.orcid0000-0003-3836-9826
dc.identifier.orcid0000-0002-3389-6734
dc.identifier.pmid21552597
dc.identifier.scopus2-s2.0-79960906989
dc.identifier.scopusqualityQ1
dc.identifier.startpage1283
dc.identifier.urihttps://doi.org/10.1039/c1pp05019b
dc.identifier.urihttps://hdl.handle.net/11129/13699
dc.identifier.volume10
dc.identifier.wosWOS:000293191700004
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakPubMed
dc.indekslendigikaynakScopus
dc.language.isoen
dc.publisherSpringernature
dc.relation.ispartofPhotochemical & Photobiological Sciences
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WoS_20260204
dc.subjectDiimide Derivatives
dc.subjectState
dc.subjectPerylenediimide
dc.subjectPolymers
dc.titleA new tunable light-emitting and ?-stacked hexa-ethyleneglycol naphthalene-bisimide oligomer: synthesis, photophysics and electrochemical properties
dc.typeArticle

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