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Abstract:
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The Schiff base, 3-hydroxyquinoxaline-2-carboxalidine-4-aminoantipyrine, was synthesized by the
condensation of 3-hydroxyquinoxaline-2-carboxaldehyde with 4-aminoantipyrine. HPLC, FT-IR and NMR
spectral data revealed that the compound exists predominantly in the amide tautomeric form and
exhibits both absorption and fluorescence solvatochromism, large stokes shift, two electron quasireversible
redox behaviour and good thermal stability, with a glass transition temperature of 104 oC. The
third-order non-linear optical character was studied using open aperture Z-scan methodology employing
7 ns pulses at 532 nm. The third-order non-linear absorption coefficient, b, was 1.48 x 10-6 cm W-1 and
the imaginary part of the third-order non-linear optical susceptibility, Im c(3), was 3.36x10-10 esu. The
optical limiting threshold for the compound was found to be 340 MW cm-2. |