Electron Accepting Perylene Dyes with Versatile Imide Substituents: Synthesis and Characterization

dc.contributor.advisorİcil, Huriye
dc.contributor.authorEltabeb, Safa Elshreef
dc.date.accessioned2019-04-29T06:29:30Z
dc.date.available2019-04-29T06:29:30Z
dc.date.issued2015-02
dc.date.submitted2015
dc.departmentEastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistryen_US
dc.descriptionMaster of Science in Chemistry. Thesis (M.S.)--Eastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistry, 2015. Supervisor: Prof. Dr. Huriye İcil.en_US
dc.description.abstractPerylene bisimides (PBIs) have received significant attention due to their exceptional photophysical and optical properties. Derivatives of PBIs show high fluorescence quantum yields, high electron affinities and large band-gaps‚ that make them excellent candidates for numerous optoelectronic devices such as light-emitting diodes, photovoltaics, optical switching, and electroluminescent devices. PBIs are considered as n-type semiconductors in which the main charge carriers are in their conduction band. On the other hand, most organic conducting substances are p-type semiconductors. In the current work, the synthesis of a new perylene bisimide N‚N′-Bis(1-methyl-2-cyanoethene)-3,4,9,10-perylenebis(dicarboxiimide) (EAPDI) was carried out. 1-methyl-2-cyanoethene substituent is specifically chosen so that the imide regions of perylene core offer better solubility and impressive optical properties of the perylene bisimide. The synthesized bisimide was approved by FT-IR and its photo-physical properties were studied by UV–vis and emission techniques. EAPDI has high molar absorptivity as well as high fluorescence quantum yields (Φf = 0.72). The absorption and emission spectra of EAPDI are mirrored images in DMF, CHCl3, MeOH with smaller Stoke shifts. Keywords: Perylene bisimide, 1-methyl-2-cyanoethene, absorbance, fluorescence.en_US
dc.description.abstractÖZ: Perylenebisimide’ler (PBIs) olağanüstü fotofiziksel ve optik özellikleri nedeniyle önemli ilgi görmüştür. PBIs Türevleri, yüksek floresan kuantum verimleri, yüksek elektron ilgileri ve geniş band aralıkları göstermekte, bu özellikler onları ışık yayan diyotlar, fotovoltaikler, optik anahtarlama, ve elektrolüminesans cihazlar gibi çok sayıda optoelektronik cihazlar için mükemmel adaylardır yapmak. PBI’ler ana yük taşıyıcıların iletkenlik bandında olmasından dolayı n-tipi yarı iletken olarak kabuledilmektedir. Diğer yandan, birçok organik iletken maddeler p-tipi yarı iletkenlerdir. Mevcut çalışmada, yeni bir perylen bisimid N,N'-Bis(1-metil-2-siyanoeten)-3,4,9,10-perilen bis(dikarboksimid) (EAPDI) sentezi gerçekleştirilmiştir. Sübstitüe 1-metil-2-siyanoetenperilenin imid bölgelerine bağlanarak daha iyi bir çözünürlük sunmaktadır ve perilen bisimidin optik özellikleri etkileyicidir. Sentezlenen bisimid,FT-IR ile kanıtlanmış ve bunun foto-fizikselözellikleri UV-Vis ve emisyon teknikleri ile çalışılmıştır. EAPDI, yüksek molar absorplama yanında yüksek floresan kuantum verimine(Φf = 0.72) sahiptir. EAPDI’in absorpsiyon ve emisyon spektrumlarıküçük Stoke kaymaları ile DMF, CHCI3, MeOH’da ayna görüntüsündedir. Anahtar: Perylenebisimid, 1-metil-2-siyanoeten, absorpsiyon, floresan.en_US
dc.identifier.citationEltabeb, Safa Elshreef. (2015). Electron Accepting Perylene Dyes with Versatile Imide Substituents: Synthesis and Characterization. Thesis (M.S.), Eastern Mediterranean University, Institute of Graduate Studies and Research, Dept. of Chemistry, Famagusta: North Cyprus.en_US
dc.identifier.urihttps://hdl.handle.net/11129/4065
dc.language.isoen
dc.publisherEastern Mediterranean University EMUen_US
dc.relation.publicationcategoryTez
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectChemistryen_US
dc.subjectDyes (Chemistry)en_US
dc.subjectPerylee Dyesen_US
dc.subjectPhotochemistryen_US
dc.subjectPerylene bisimideeen_US
dc.subject1-methyl-2-cyanoetheneen_US
dc.subjectabsorbanceen_US
dc.subjectfluorescencen_US
dc.titleElectron Accepting Perylene Dyes with Versatile Imide Substituents: Synthesis and Characterizationen_US
dc.typeMaster Thesis

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