journal article·2020-12

Spectroscopic and third-order nonlinear optical properties of organic single-crystal 2-picolinictrichloroacetate: an overview

N Manopradha, S Gowri, S Rama, K Selvaraju, K Kirubavathi, G Vinitha

Bulletin of Materials Science· Volume 43· Issue 1
Publisher page

Abstract

Organic single crystals of 2-picolinictrichloroacetate (PTCA) have been successfully grown by slow evaporation technique. The structural and optical characterization of the PTCA is analysed experimentally by Fourier transform infrared and UV–visible spectroscopic technique and theoretical studies, by density functional theory method. The charge transfer interactions leading to nonlinear properties taking place in the molecule have been studied by highest energy occupied molecular orbital and lowest energy unoccupied molecular orbital analysis and natural bond orbital analysis. Open-aperture Z-scan results on evaluating the nonlinear optical properties experimentally, confirm these materials as good optical limiters. In addition, the PTCA exhibits a blue luminescence emission which shows that it is a potential material for OLED device applications.
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Research context

OpenAlex topics: Nonlinear Optical Materials Research · Nonlinear Optical Materials Studies · Crystal structures of chemical compounds

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

References (21)

Show source-provided references
1. Gao S, Chen W, Wang G and Chen J 2006 J. Cryst. Growth 297 36110.1016/j.jcrysgro.2006.09.047 ↗
2. Uma Devi T, Lawrence N, Ramesh Babu R, Ramamurthi K and Bhagavannarayana G 2009 Spectrochim. Acta A Mol. Biomol. Spectrosc. 71 166710.1016/j.saa.2008.06.034 ↗
3. Jagannathan K, Kalainathan S, Gnanasekaran T, Vijayan N and Bhagavannarayana G 2007 Cryst. Res. Technol. 42 47110.1002/crat.200610852 ↗
4. Gowri S, Uma Devi T, Alen S, Sajan D, Surendra Dilip C and Vinitha G 2018 J. Mater. Sci.: Mater. Electron. 29 19710
5. Gowri S, Anitha K, Suresh A, Uma Devi T, Selvanayagam S, Sajan D et al 2012 Spectrochim. Acta A Mol. Biomol. Spectrosc. 95 7310.1016/j.saa.2012.04.002 ↗
6. Frisch M J, Trucks G W, Schlegel H B, Scuseria G E, Robb M A, Cheeseman J R et al 2009 Gaussian 09 revision A. Wallingford, CT: 02 Gaussian Inc.
7. Schlegel B 1982 J. Comp. Chem. 3 21410.1002/jcc.540030212 ↗
8. Dennington R, Keith T and Millam J 2009 GaussView Version 5 Semichem Inc., Shawnee Mission, KS
9. Matsuzawa N, Ata M and Dixon D A 1995 J. Phys. Chem. 99 769810.1021/j100019a058 ↗
10. Sasikala V, Sajan D, Vijayan N, Chaitanya K, Babu Raj M S and Selin Joy B H 2014 Spectrochim. Acta A Mol. Biomol. Spectrosc. 123 12710.1016/j.saa.2013.12.045 ↗
11. Gilman J 1977 Mater. Res. Innov. 1 7110.1007/s100190050023 ↗
12. Chitrambalam S, Manimaran D, Joe I H, Rastogi V K and Hassan I U 2018 Opt. Mater. 75 28510.1016/j.optmat.2017.10.003 ↗
13. Spackman M A and Byrom P G 1977 Chem. Phys. Lett. 267 21510.1016/S0009-2614(97)00100-0 ↗
14. Spackman M A and McKinnon J J 2004 CrystEngComm 4 37810.1039/B203191B ↗
15. Hirshfeld F L 1977 Theor. Chim. Acta 44 12910.1007/BF00549096 ↗
16. Spackman M A and Jayatilaka D 2009 CrystEngComm. 11 1910.1039/B818330A ↗
17. Senthil K, Kalainathan S, Ruban Kumar A and Aravindan P G 2014 RSC Adv. 4 5611210.1039/C4RA09112D ↗
18. Nivetha K, Kalainathan S, Yamada M, Kondo Y and Hamada F 2016 RSC Adv. 6 3597710.1039/C6RA02544G ↗
19. Wang J and Blau W J 2011 J. Opt. A: Pure Appl. Opt. 11 02400110.1088/1464-4258/11/2/024001 ↗
20. Henari F Z, Balu W J, Milgrom L R, Yahyoglu G, Philips D and Lacey J A 1977 Chem. Phys. Lett. 267 22910.1016/S0009-2614(97)00112-7 ↗
21. Henari F Z 2001 J. Opt. A: Pure Appl. Opt. 3 18810.1088/1464-4258/3/3/306 ↗