DSpace
 

EMU I-REP >
08 Faculty of Arts and Sciences >
Department of Chemistry >
Theses (Master's and Ph.D) – Chemistry >

Please use this identifier to cite or link to this item: http://hdl.handle.net/11129/4065

Title: Electron Accepting Perylene Dyes with Versatile Imide Substituents: Synthesis and Characterization
Authors: İcil, Huriye
Eltabeb, Safa Elshreef
Eastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistry
Keywords: Chemistry
Dyes (Chemistry)
Perylee Dyes
Photochemistry
Perylene bisimidee
1-methyl-2-cyanoethene
absorbance
fluorescenc
Issue Date: Feb-2015
Publisher: Eastern Mediterranean University EMU
Citation: Eltabeb, 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.
Abstract: Perylene 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.
ÖZ: 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.
Description: Master of Science in Chemistry. Thesis (M.S.)--Eastern Mediterranean University, Faculty of Arts and Sciences, Dept. of Chemistry, 2015. Supervisor: Prof. Dr. Huriye İcil.
URI: http://hdl.handle.net/11129/4065
Appears in Collections:Theses (Master's and Ph.D) – Chemistry

Files in This Item:

File Description SizeFormat
EltabebSafa.pdfThesis, Master1.48 MBAdobe PDFView/Open


This item is protected by original copyright

Recommend this item
View Statistics

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

 

Valid XHTML 1.0! DSpace Software Copyright © 2002-2010  Duraspace - Feedback