Synthesis and Optical properties of New Perylene Derivatives

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dc.contributor.advisor İcil, Huriye
dc.contributor.author Galabe, Emile Muah
dc.date.accessioned 2018-05-31T11:45:54Z
dc.date.available 2018-05-31T11:45:54Z
dc.date.issued 2014-06
dc.date.submitted 2014-06
dc.identifier.citation Galabe, Emile Muah. (2014). Synthesis and Optical properties of New Perylene Derivatives. Thesis (M.S.), Eastern Mediterranean University, Institute of Graduate Studies and Research, Dept. of Chemistry, Famagusta: North Cyprus. en_US
dc.identifier.uri http://hdl.handle.net/11129/3746
dc.description Master of Science in Chemistry. Thesis (M.S.)--Eastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistry, 2014. Supervisor: Prof. Dr. Huriye İcil. en_US
dc.description.abstract Versatile substituents of perylene chrmophores creates higher absorptions in visible region of absorption spectrum and also exhibits higher coefficients of molar extinction. Furthermore, they have the ability to emit light of almost unitary which signifies higher fluorescence quantum yields. Perylene dyes acts a major role in dye sensitized solar cells due to the presence of four carbonyl groups in its core which creates ease of accepting an electron. In this research, N,N′-Bis(3,3,5,5-tetramethyl-4-piperidinyl)-3,4,9,10-perylenebis (dicarboximide) (PPDI) and N-(3,3,5,5-tetramethyl-4-piperidinyl)-3,4,9,10-perylenetetracarboxylic-3,4-anhydride-9,10-imide (PPMI) were sensitized and comparison of their photophysical properties were carried out. FTIR spectroscopy was used to characterize the compounds and their photophysical properties analyzed via absorption and emission spectroscopy. All the perylene dyes synthesized showed very high molar absorptivity with the highest being 152000 M-1cm-1 obtained from PPMI. PPMI absorption spectrum shows a 4 nm blue shift in a polar aprotic solvent as a result of increased level of polarity and the stabilization of PPMI energy levels it induces on the structure. Keywords: Perylene diimide, perylene tetracarboxylic acid, perylene monoimde, perylene carboxylic acid monoimide. en_US
dc.description.abstract ÖZ : Çok Yönlü atomuna no oluşturur perylene chrmophores emilimler daha yüksek görünen bölge absorpsiyon spektrumu ve olduysa da daha yüksek varyasyon katsayıları molar sönme. Ayrıca, ışık yaydığından yeteneğine sahip olan hemen hemen devletin üniter anlamına gelmektedir uygulandığında flüoresans üreten kendinden aydınlatmalı kuvantum verimleri daha yüksek. Görevi görür Perylene boyalar önemli bir rol boya pozlandırmadan güneş enerjisi hücreleri bulunması nedeniyle dört carbonyl grubu oluşturan, temel kabul kolaylığı bir elektron. Bu araştırma, N, N' -Bis(3,3,5,5-tetramethyl-4-piperidinyl)-3,4,9,10-perylenebis (dicarboximide) (PPDI) ve N- (3,3,5,5-tetramethyl-4-piperidinyl)-3,4,9,10-perylenetetracarboxylic-3,4-anhidrit-9,10-imide (PPMI) pozlandırmadan ve karşılaştırma, photophysical özellikleri gerçekleştirildi. FTIR spektroskopi, karakterize etmek için kullanılan bileşikler ve onların photophysical özellikleri üzerinden analiz emilim ve emisyon spektroskopi. Gösterdi Tüm perylene boyalar sentezlenmiş çok yüksek molar absorptivity olan en yüksek 152000 M-1cm-1 elde PPMI. PPMI absorpsiyon spektrumu 4 nm mavi gösterir vardiya kutup ayısı aprotic solvent sonuç olarak artan düzeyde polarite ve stabilizasyonu PPMI enerji seviyelerine yankılanmaya neden olur. Anahtar Sözcükler: Perylene diimide, perylene tetracarboxylic asit, perylene monoimde, perylene carboxylic asit monoimide. en_US
dc.language.iso eng en_US
dc.publisher Eastern Mediterranean University (EMU) - Doğu Akdeniz Üniversitesi (DAÜ) en_US
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject Chemistry en_US
dc.subject Dyes (Chemistry) en_US
dc.subject Perylene Dyes en_US
dc.subject Photochemistry en_US
dc.subject Perylene diimide en_US
dc.subject perylene tetracarboxylic acid en_US
dc.subject perylene monoimde en_US
dc.subject perylene carboxylic acid monoimide en_US
dc.title Synthesis and Optical properties of New Perylene Derivatives en_US
dc.type masterThesis en_US
dc.contributor.department Eastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistry en_US


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