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

No Thumbnail Available

Date

2013

Journal Title

Journal ISSN

Volume Title

Publisher

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.

Description

Keywords

5-oxazolones, Fluorescent probes, Nonlinear absorption coefficient, Nonlinear refractive index, Optical limiting, Third order nonlinear optical properties, Third-order, Third-order susceptibility, Nuclear magnetic resonance spectroscopy, Optical properties, Refractive index, Two photon processes, Nonlinear optics

Citation

Dyes and Pigments, 2013, 99, 3, pp. 713-719

Collections

Endorsement

Review

Supplemented By

Referenced By