Please use this identifier to cite or link to this item: https://doi.org/10.1039/b901847f
Title: Effect of substituents on the electron transport properties of bay substituted perylene diimide derivatives
Authors: Vajiravelu, S. 
Ramunas, L.
Juozas Vidas, G.
Valentas, G.
Vygintas, J.
Valiyaveettil, S. 
Issue Date: 2009
Citation: Vajiravelu, S., Ramunas, L., Juozas Vidas, G., Valentas, G., Vygintas, J., Valiyaveettil, S. (2009). Effect of substituents on the electron transport properties of bay substituted perylene diimide derivatives. Journal of Materials Chemistry 19 (24) : 4268-4275. ScholarBank@NUS Repository. https://doi.org/10.1039/b901847f
Abstract: Electron donating substituents such as 3,4,5-trimethoxy phenyl (PDI1), thiophene (PDI2), 6-methoxy naphthyl (PDI3), 5-hexyl dithiophene (PDI4) and thioanthrenyl (PDI5) moieties incorporated at the bay region of N,N′-dodecylperylene diimide (PDI) derivatives have been synthesized and characterised. The absorption maxima of PDI1-5 showed a bathochromic shift with considerable peak broadening and merging of vibronic fine structure as compared to that of PDI. The photoinduced intramolecular charge transfer (ICT) from electron donating substituents to the perylene-acceptor has been observed from fluorescence self-quenching. The molecules are stable up to 400 °C and amorphous in nature. The cyclic voltammetry results revealed that the oxidation potential can be tuned by the electron donating capacity of the substituents and the dithiophene-attached perylene derivative (PDI4) showed a very low band gap of 1.57 eV. The electron transporting properties have been studied using xerographic time-of-flight method and the highest electron mobility reached up to 4.4 × 10-4 cm2 V-1 s-1 at 6.4 × 105 V cm-1 for 1,7-di(3,4,5-trimethoxyphenyl) perylene diimide (PDI1) under ambient conditions. © 2009 The Royal Society of Chemistry.
Source Title: Journal of Materials Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/93656
ISSN: 09599428
DOI: 10.1039/b901847f
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