journal article·2013-01

Non-linear optical analyses of nitro aniline derived Schiff bases of 9-anthraldehyde

S. Vijayalakshmi, S. Kalyanaraman

Optical Materials· Volume 35· Issue 3
Publisher page

Abstract

Abstract The synthesis and non-linear optical properties of nitro aniline derived Schiff bases of 9-anthraldehyde were carried out. The compounds were characterized using FT-IR, Raman and UV–Vis spectroscopies. The FT-IR and Raman spectral data revealed the confirmation of Schiff bases with the absorption band assignable to the stretching of C N band. The charge transfer (CT) interaction between the donor and acceptor molecules were confirmed through λ max of the UV–Vis spectra. The UV–Vis analysis indicated, bathochromic shift in the compounds, implying a non-zero first order molecular hyperpolarizability ( β ) which are translated into macroscopic non-linearity χ 2 . To investigate the solid state macroscopic non-zero non-linear optical response, χ 2 , (second harmonic generation) the Kurtz and Perry method was used. This happens to be the first report on the non-linear optical analysis of these compounds.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nonlinear Optical Materials Research · Molecular spectroscopy and chirality · Nonlinear Optical Materials Studies

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (30)

Show source-provided references
1. Unwar · J. Mol. Struct. · 2006 · 800 · 1810.1016/j.molstruc.2006.03.089 ↗
2. Sajan · Vib. Spectrosc. · 2010 · 54 · 7210.1016/j.vibspec.2010.06.007 ↗
3. Bosshard · Phys. Rev. B · 2000 · 61 · 1068810.1103/PhysRevB.61.10688 ↗
4. Ji · J. Phys. Chem. B · 2003 · 107 · 1104310.1021/jp0347116 ↗
5. He · J. Chem. Phys. · 2004 · 120 · 527510.1063/1.1647537 ↗
6. Handbook of advanced electronic materials and devices
7. Kanis · Chem. Rev. · 1994 · 195 · 94
8. Prasad · 1991
9. Marder · 1991
10. Munn · 1993
11. Bhat · Mater. Chem. Phys. · 1996 · 44 · 26110.1016/0254-0584(96)80066-6 ↗
12. Oudar · J. Chem. Phys. · 1977 · 67 · 44610.1063/1.434888 ↗
13. Katz · Proc. SPIE · 1983 · 824 · 86
14. Trujillo · Inorg. Chem. · 2010 · 49 · 275010.1021/ic902126a ↗
15. Rivera · J. Organomet. Chem. · 2006 · 691 · 172210.1016/j.jorganchem.2005.12.038 ↗
16. Lacroix · Eur. J. Inorg. Chem. · 2001 · 2001 · 33910.1002/1099-0682(200102)2001:2<339::AID-EJIC339>3.0.CO;2-Z ↗
17. Lacroix · Chem. Mater. · 1996 · 8 · 54110.1021/cm950426q ↗
18. Costes · Inorg. Chem. · 2005 · 44 · 197310.1021/ic048578n ↗
19. Kulakowska · Eur. Polym. J. · 2000 · 36 · 180510.1016/S0014-3057(99)00268-2 ↗
20. Prabhu · J. Cryst. Growth · 2001 · 233 · 37510.1016/S0022-0248(01)01507-X ↗
21. Breigleb · Electrochem. (Ber. Bausengesell. Physiki Chem.) · 1960 · 64 · 347
22. Prabhumirashi · Spectrochim. Acta · 1986 · 42A · 43510.1016/0584-8539(86)80036-8 ↗
23. delower · Opt. Mater. · 2010 · 32 · 66910.1016/j.optmat.2009.07.002 ↗
24. Bartkowiak · J. Mol. Model · 2005 · 11 · 31710.1007/s00894-005-0249-6 ↗
25. Dyall · Spectrochim. Acta · 1961 · 17 · 29110.1016/0371-1951(61)80075-1 ↗
26. Huysken · J. Chem. Phys. · 1998 · 108 · 816110.1063/1.476171 ↗
27. Anne myers kelley
28. Zyss · Phys. Rev. A · 1982 · 26 · 201610.1103/PhysRevA.26.2028 ↗
29. Twieg · 1983
30. Kurtz · J. Appl. Phys. · 1968 · 39 · 379810.1063/1.1656857 ↗