EN
A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules
Abstract
The aim of this
article is to inform about perylene-3,4,9,10-tetracarboxylic acid dimide (PDI)
derivatives. Also, it is to give short and simple information about optical
properties and using fields. Perylene-3,4,9,10-tetracarboxylic acid dimide
derivatives known as perylene diimides are material
of highly conjugated molecule. PDIs exhibit strong absorptions within
the range of 400-450 nm (B band) and 500-700 nm (Q band). Perylene diimide dyes show generally characteristic
absorption peaks at 458, 490, 526 nm. These absorption peaks are matched by the
corresponding emission peaks at 540, 576, 624 nm, respectively. It has donor
core and acceptor carbonyl groups. Perylene dimide has good electron
mobility, high fluorescence quantum yields, strong absorption in the visible
region, photostability, thermal
stability, good semi-conductivity. These properties
benefit them application of electronic material. Applications of PDIs are in
the field of photo-electronic material, dye lasers, organic light-emitting diodes,
and chemosensing materials.
Keywords
References
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- [4] Saeed, A.; Shabir, G.; Mahar, J.; Irfan, M. Spectro-scopic and Electrochemical Behavior of Newly Synthe-sized High Fluorescent Symmetric 4′-nitrophenyl-3,4,9,10-perylenebisdiimide-azo Hybrid Dyes. Spectro-chimica Acta Part A: Molecular and Biomolecular Spec-troscopy. 2015; 151, 72-79.
- [5] Rachford, A.A.; Goeb, S.; Castellano, F.N. Accesing the Excited State in Perylenediimides. American Chem-ical Society. 2008; 130, 2766-2767.
- [6] Georgiev, N.I.; Sakr, A.R.; Bojinov.V.B. Design and Synthesis of Novel Fluorescence Sensing Perylene Diimides Based on Photoinduced Electron Transfer. Dyes and Pigments. 2011; 91, 332-339.
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Details
Primary Language
English
Subjects
Engineering
Journal Section
Research Article
Authors
Publication Date
June 30, 2017
Submission Date
November 19, 2016
Acceptance Date
January 7, 2017
Published in Issue
Year 2017 Volume: 13 Number: 2
APA
Birel, Ö. (2017). A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules. Celal Bayar University Journal of Science, 13(2), 379-386. https://doi.org/10.18466/cbayarfbe.319879
AMA
1.Birel Ö. A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules. CBUJOS. 2017;13(2):379-386. doi:10.18466/cbayarfbe.319879
Chicago
Birel, Özgür. 2017. “A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules”. Celal Bayar University Journal of Science 13 (2): 379-86. https://doi.org/10.18466/cbayarfbe.319879.
EndNote
Birel Ö (June 1, 2017) A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules. Celal Bayar University Journal of Science 13 2 379–386.
IEEE
[1]Ö. Birel, “A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules”, CBUJOS, vol. 13, no. 2, pp. 379–386, June 2017, doi: 10.18466/cbayarfbe.319879.
ISNAD
Birel, Özgür. “A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules”. Celal Bayar University Journal of Science 13/2 (June 1, 2017): 379-386. https://doi.org/10.18466/cbayarfbe.319879.
JAMA
1.Birel Ö. A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules. CBUJOS. 2017;13:379–386.
MLA
Birel, Özgür. “A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules”. Celal Bayar University Journal of Science, vol. 13, no. 2, June 2017, pp. 379-86, doi:10.18466/cbayarfbe.319879.
Vancouver
1.Özgür Birel. A Review on Perylene-3,4,9,10-Tetracarboxylic Acid Diimide Molecules. CBUJOS. 2017 Jun. 1;13(2):379-86. doi:10.18466/cbayarfbe.319879
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