Please use this identifier to cite or link to this item:
https://idr.l4.nitk.ac.in/jspui/handle/123456789/13299
Title: | Synthesis, characterization and evaluation of the photophysical and nonlinear optical behaviour of novel 4-substituted arylidene-2-[5-(2,6- dichlorophenyl)-3-methyl-1,2-oxazol-4-yl]-1,3-oxazol-5-ones |
Authors: | Murthy, Y.L.N. Suhasini, K.P. Veeraiah, V. Umesh, G. Manjunatha, K.B. Christopher, V. |
Issue Date: | 2013 |
Citation: | Dyes and Pigments, 2013, Vol.99, 3, pp.713-719 |
Abstract: | Five new 4-substituted arylidene-2-[5-(2,6-dichlorophenyl)-3-methyl-1,2- oxazol-4-yl]-1,3-oxazol-5-ones have been designed and synthesized in order to study their third-order nonlinear optical properties. These novel compounds were characterized by advanced spectroscopic techniques (IR, 1H, 13C NMR, ESI-MS spectroscopy and elemental analyses). In addition, the evaluation of absorption and emission wavelengths of the new 5-oxazolone derivatives was carried out in seven different solvents of varying polarity, which showed intense absorption maxima at 350-480 nm and emission maxima at 390-535 nm respectively. The third-order nonlinear optical properties of the target molecules have been investigated in N,N-dimethylformamide using a single beam Z-scan technique with nanosecond laser pulses at 532 nm. The nonlinear refractive index, nonlinear absorption coefficient, magnitude of third-order susceptibility and molecular two photon absorption cross-sections have been determined. All of the compounds showed excellent optical limiting behaviour at 532 nm, with the best optical limiting behaviour observed with strong electron donor [dimethyl and N,N-diethyl amino] substituents. 2013 Elsevier Ltd. All rights reserved. |
URI: | http://idr.nitk.ac.in/jspui/handle/123456789/13299 |
Appears in Collections: | 1. Journal Articles |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.