Fluorescence, spectroscopic and NLO properties of green tea extract in deoxyribonucleic acid
Source abstract
Abstract
Abstract Natural, purely biological deoxyribonucleic acid (DNA)–green tea extract (GTE) complexes at different concentrations were prepared and characterized for their spectroscopic, fluorescent, linear and nonlinear optical properties. The complexes can be processed into good optical quality thin films by solution casting. They fluoresce when excited in UV absorption band, with a significantly larger quantum yield for the DNA–GTE complex than for a pure GTE solution. The thin film refractive indices were determined by Fabry–Perot (FP) interference patterns. The third-order nonlinear optical (NLO) properties of thin films were determined by the optical third-harmonic generation technique at 1064.2 nm fundamental wavelength. The phase of THG susceptibility was determined from the concentration variation of THG susceptibility. It reveals presence of a two-photon resonance with a band lying in the optical gap.
Source: openaire · Quality: candidate unverified · Source record ↗
Research context
OpenAlex topics: Protein Interaction Studies and Fluorescence Analysis · Photochemistry and Electron Transfer Studies · Nonlinear Optical Materials Studies
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
References (26)
Show source-provided references
1. Watson · Nature · 1953 · 171 · 73710.1038/171737a0 ↗
2. Crick · Proc. Royal Soc. (London) · 1954 · 223 · 8010.1098/rspa.1954.0101 ↗
3. Rau · Compt. Rend. Acad. Sci. · 2012 · 13 · 85310.1016/j.crhy.2012.09.005 ↗
4. Wang · Chem. Mater. · 2001 · 13 · 127310.1021/cm000869g ↗
5. Zhang · Proc. SPIE · 2001 · 4580 · 33710.1117/12.444982 ↗
6. Iosub · Opt. Mater. · 2012 · 34 · 164410.1016/j.optmat.2012.03.020 ↗
7. B. O’Regan, M. Grätzel, Nature 353 (6346) 737–740 http://dx.doi.org/10.1038/353737a0 (Bibcode 1991 Natur.353.737O).10.1038/353737a0 ↗
8. Thielecke · Phytochem. · 2009 · 70 · 1110.1016/j.phytochem.2008.11.011 ↗
9. Xu · Antiviral Research · 2008 · 78 · 24210.1016/j.antiviral.2007.11.011 ↗
10. Kaur · Brain Cognition · 2008 · 67 · 2510.1016/j.bandc.2007.10.003 ↗
11. Yang · Techn. Appl. Pharmac. · 2007 · 224 · 26510.1016/j.taap.2006.11.024 ↗
12. Babu · Chemico–Biolog. Interac. · 2006 · 162 · 11410.1016/j.cbi.2006.04.009 ↗
13. Weiss · J. Chromatogr. A · 2006 · 1117 · 10310.1016/j.chroma.2006.03.057 ↗
14. Yu · Appl. Opt. · 2006 · 46 · 150710.1364/AO.46.001507 ↗
15. Yu · Proc. SPIE · 2007 · 6470 · 64700V10.1117/12.701429 ↗
16. Kajzar · J. Appl. Phys. · 1986 · 60 · 304010.1063/1.337759 ↗
17. Kajzar · 1998 · 767
18. Van Beek · J. Chem. Phys. · 1991 · 95 · 640010.1063/1.461560 ↗
19. Van Beek · Chem. Phys. · 1992 · 161 · 29910.1016/0301-0104(92)80197-4 ↗
20. Torruellas · Chem. Phys. Lett. · 1990 · 175 · 1110.1016/0009-2614(90)85510-J ↗
21. Rau · J. Comp. Method Sci. Eng. · 2010 · 10 · 531
22. Manea · Opt. Mat. · 2013 · 35 · 109910.1016/j.optmat.2012.12.027 ↗
23. Grote · Mol. Cryst. Liq. Cryst. · 2005 · 426 · 310.1080/15421400590890615 ↗
24. Krupka · Thin Solid Films · 2008 · 516 · 893210.1016/j.tsf.2007.11.089 ↗
25. Gubler · Phys. Rev. B · 2000 · 61 · 1070210.1103/PhysRevB.61.10702 ↗
26. Morichere · Proc. SPIE · 1991 · 1560 · 21410.1117/12.50719 ↗