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Year 2025, Volume: 26 Issue: 3, 188 - 202, 25.09.2025
https://doi.org/10.18038/estubtda.1624326

Abstract

Project Number

202019059

References

  • [1] Marder SR, Organic nonlinear optical materials Where we have been and where we are going, Chemical Communications 2006;37;131-4.
  • [2] Mehkoom M, Afzal M, Ahmad S, Khan SA. The new pyrazoline derivative 5‐(3,4-Dimethoxy‐phenyl)‐3‐(2,5‐dimethyl‐thiophene‐3‐yl),‐4,5‐dihydro‐pyrazole‐1‐carbothioic acid amide (DDPA) as an advisable candidate for optical linearity, nonlinearity, and limiting performance. J Mol Liq 2022;345;117018.
  • [3] Gong P, Liu X, Kang L, Lin Z. Inorganic planar π-conjugated groups in nonlinear optical crystals: Review and Outlook. Inorganic Chemistry Frontiers 2020;7;839-852.
  • [4] Evans OR, Lin W. Crystal engineering of NLO materials based on metal-organic coordination networks. Ac Chem Res 2002; 35; 511–522.
  • [5] Abrinaei F, Kimiagar S, Gharedaghi S. Strong optical nonlinearity of CdS/nitrogen-doped reduced graphene oxide nanocomposites using Z-scan technique. Journal of Materials Science: Materials in Electronics 2018; 29; 2550–2560.
  • [6] Alamouti AF, Nadafan M, Dehghani Z, Ara MHM, Noghreiyan AV. Structural and Optical Coefficients Investigation of γ-Al2O3 Nanoparticles using Kramers-Kronig Relations and Z–scan Technique. Journal of Asian Ceramic Societies 2021; 9; 366–373.
  • [7] Dehghani Z, Nadafan M, Saievar IE. The effect of external applied fields on the third order nonlinear susceptibility of ferro-nematics. J Mol Liq 2015; 204; 70–75.
  • [8] Abrinaei F. Laser ablation of magnesium in water and investigation of optical nonlinearity by the Z-scan technique. Journal of the Optical Society of America B 2016; 33; 864.
  • [9] Hasmuddin M, Abdullah MM, Singh P, Shkir M, Vijayan N, Wahab MA. Ab-initio study of L-Tartaric Acid (LTA) single crystal for NLO application, Opt Laser Technol 2015; 74; 53–59.
  • [10] Jagadesan A, Sivakumar N, Mohan KR, Chakkaravarthi G, Arjunan S. Synthesis, crystal structure, growth and characterization of an optical organic material: 4-Aminopyridinium Trichloro acetate single crystal. Opt Mater 2018; 84; 864–869.
  • [11] Kwon SJ, Jazbinsek M, Kwon OP, Günter P. Crystal Growth and Morphology Control of OH1 Organic Electrooptic Crystals. Cryst Growth Des 2010; 10; 1552–1558.
  • [12] Sabaa MW, Elzanaty AM, Abdel-Gawad OF, Arafa EG. Synthesis, characterization and antimicrobial activity of Schiff bases modified chitosan-graft-poly(acrylonitrile). Int J Biol Macromol 2017; 109; 1280–1291.
  • [13] Poonia K, Siddiqui S, Arshad M, Kumar D. In vitro anticancer activities of Schiff base and its lanthanum complex. Spectrochim Acta A Mol Biomol Spectrosc 2016; 155; 146–154.
  • [14] Inan A, İkiz M, Tayhan SE, Bilgin S, Genç N. Antiproliferative, antioxidant, computational and electrochemical studies of new azo-containing Schiff base ruthenium(II) complexes. New Journal of Chemistry 2018; 42; 2952–2963.
  • [15] Leela S, Ramamurthi K, Bhagavannarayana G, Synthesis, growth, spectral, thermal, mechanical and optical properties of 4-chloro-4′dimethylamino-benzylidene aniline crystal: A third order nonlinear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2009; 74; 78–83.
  • [16] Leela S, Hema R, Stoeckli EH, Ramamurthi K, Bhagavannarayana G. Design, synthesis, growth and characterization of 4-methoxy-4′- dimethylamino-benzylidene aniline (MDMABA): A novel third order nonlinear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2010; 77; 927–932.
  • [17] Leela S, Deepa RT, Subashini A, Brindha S, Ramesh BR, Ramamurthi K. Studies on growth and characterization of nonlinear optical material 4-chloro-4′methoxy benzylideneaniline: A Schiff base organic material. Arabian Journal of Chemistry 2017; 10; S3974–S3981.
  • [18] Subashini A, Kumaravel R, Leela S, Evans HS, Sastikumar D, Ramamurthi K, Synthesis, growth and characterization of 4-bromo-4′chloro benzylidene aniline - A third order non linear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2011; 78; 935–941.
  • [19] Subashini A, Bhagavannarayana G, Ramamurthi K. Synthesis, growth, optical, mechanical, dielectric and thermal properties of 4-chloro-4′-chlorobenzylidene aniline single crystal. Spectrochim Acta A Mol Biomol Spectrosc 2011; 82; 91–96.
  • [20] Czekalla GB. Elektronenuberfuhrung durch Lichtabsorption und-emission in Ele ktronen-Donator-Acceptor-Komplexen. Angewandte Chemie 1960;72;401-413.
  • [21] Shafiee A, Yahaya M.Determination of HOMO and LUMO of [6,6]-Phenyl C61-butyric Acid 3-ethylthiophene Ester and Poly (3-octyl-thiophene-2, 5-diyl) through Voltametry Characterization (Penentuan HOMO dan LUMO Asid [6,6]-Fenil C61-butirik Ester 3-etiltiofena dan Poli (3-oktil-tiiofena-2, 5-diyl) menerusi Pencirian Voltametri). Sains Malaysiana 2011; 40(2), 173-176.
  • [22] Runge E, Gross EKU. Density-Functional Theory for Time-Dependent Systems. Phys Rev Lett 1984; 52; 997–1000.
  • [23] Turkoglu G, Cinar ME, Buyruk A, Tekin E, Mucur SP, Kaya K, Ozturk T. Novel organoboron compounds derived from thieno[3,2-b] thiophene and triphenylamine units for OLED devices. J Mater Chem C Mater 2016; 4; 6045–6053.
  • [24] Wałęsa Chroab M, Tremblay MH, Skene WG. Hydrogen-Bond and Supramolecular-Contact Mediated Fluorescence Enhancement of Electrochromic Azomethines. Chemistry - A European Journal 2016; 22; 11382–11393.
  • [25] Salih KSM. Synthesis, characterization, surface analysis, optical activity and solvent effects on the electronic absorptions of Schiff base-functionalized amino thiophene derivatives: Experimental and TD-DFT investigations. J Mol Struct 2021; 1244;131267.
  • [26] Sıvrıkaya Y, Sakarya HC, Kiliç G, Ektı SF, Yandimoğlu M. New pyrene and fluorene-based π-conjugated Schiff bases: Theoretical and experimental investigation of optical properties. Journal of the Serbian Chemical Society 2024; 89; 1025–1038.
  • [27] Runge E, Gross EKU. Density-Functional Theory for Time-Dependent Systems. Physical Review Letters 1984;52;12.
  • [28] Becke AD. Density-functional thermochemistry. III. The role of exact Exchange. J Chem Phys 1993; 98; 5648–5652.
  • [29] Lee C, Yang W, Parr RG. Development of the Colic-Salvetti correlation-energy formula into a functional of the electron density. Phys Rev B 1988;37;785-789.
  • [30] Storm AT, Gjikaj M, Namyslo JC, Adams J, Schmidt A. 1,3-Thiazolium-4-aminides: Syntheses and Characterization of Fluorescent Mesoionic Compounds. European J Org Chem 2021; 34; 4803–4815.
  • [31] Cossi M, Rega N, Scalmani G, Barone V, Energies, Structures, and Electronic Properties of Molecules in Solution with the C-PCM Solvation Model. Comput Chem 2003;24;669-81.
  • [32] Barone V, Cossi M. Quantum Calculation of Molecular Energies and Energy Gradients in Solution by a Conductor Solvent Model. The Journal of Physical Chemistry A 1998;102;1995-2001.
  • [33] Underwood SJ, Douglas CJ. N-Pyridylimidates as Traceless Acyl Equivalents for Directed C-O Bond Functionalization. Organic Letters 2023;25;146-151.
  • [34] Lu T, Chen F. Multiwfn: A multifunctional wavefunction analyzer. J Comput Chem 2012; 33; 580–592.
  • [35] Humphrey W, Dalke A, Schulten K. VMD: Visual Molecular Dynamics. J Mol Graph 1996;1;33-8.
  • [36] Williams DJ, DS. Prasad PN. Introduction to Nonlinear Optical Effects in Molecules and Polymers. New York NY, USA;wiley; 1991.
  • [37] Vennila P, Govindaraju M, Venkatesh G, Kamal C. Molecular structure, vibrational spectral assignments (FT-IR and FT-RAMAN), NMR, NBO, HOMO-LUMO and NLO properties of O-methoxybenzaldehyde based on DFT calculations. J Mol Struct 2016; 1111; 151–156.
  • [38] Ergürhan O, Gürhan R, Parlak C, Alver Ö. Nonlinear Optical and Spectral Properties Of Hydroquinone & Fullerene Systems. Eskişehir Teknik Üniversitesi Bilim ve Teknoloji Dergisi B - Teorik Bilimler 2021; 9; 47–53.
  • [39] Abbaz T, Bendjeddou A, Villemin D. Structural and quantum chemical studies on aryl sulfonyl piperazine derivatives. Journal of Drug Delivery and Therapeutics 2019; 9; 88–97.

AN EXPERIMENTAL–THEORETICAL INSIGHT INTO SYNTHESIS AND OPTICAL PROPERTIES OF STRUCTURALLY TUNED Π-CONJUGATED SCHIFF BASES

Year 2025, Volume: 26 Issue: 3, 188 - 202, 25.09.2025
https://doi.org/10.18038/estubtda.1624326

Abstract

Novel Schiff bases 3a, 3b, and 3c were synthesized, and their optical properties were investigated through experimental methods focusing on the determination of optical band gaps (Eg) derived from UV/Vis absorption spectra. These compounds are identified as N-(6-methylbenzo[d]thiazol-2-yl)-1-(pyren-1-yl)methanimine (3a), 1-(anthracen-9-yl)-N-(6-methylbenzo[d]thiazol-2-yl)methanimine (3b), and 1-(9H-fluoren-2-yl)-N-(6-methylbenzo[d]thiazol-2-yl)methanimine (3c). To reveal the key structural and optical characteristics of these molecules, theoretical calculations were performed using Density Functional Theory (DFT) and Time-Dependent DFT (TD-DFT) at the B3LYP/6–31G(d,p) level. Theoretical results were compared with experimental data to comprehensively evaluate molecular geometries, UV/Vis spectroscopic parameters, and frontier molecular orbital (FMO) energy levels. Nonlinear optical (NLO) properties were analyzed in relation to molecular structure, substitution patterns, conjugation length, and intramolecular charge transfer (ICT) characteristics. The calculated first-order hyperpolarizability (β) values for compounds 3a, 3b, and 3c in DMSO were found to be 4379.6, 7261.4, and 7434.4 a.u., respectively, approximately 110, 183, and 187 times higher than that of the standard reference compound urea. These findings indicate that the synthesized Schiff bases are promising candidates for future applications in photonics and optoelectronics.

Ethical Statement

I confirm that the manuscript has been read and approved by all named authors for submission to the Eskişehir Technical University Journal of Science and Technology A-Applied Sciences and Engineering.

Supporting Institution

Eskişehir Osmangazi University Scientific Research Projects Council for financial support (Project No 202019059)

Project Number

202019059

Thanks

The authors thank the Eskişehir Osmangazi University Scientific Research Projects Council for financial support (Project No 202019059). We would also like to thank our graduate student Sevgi ŞEN from Eskişehir Technical University for her help in the physical arrangement of the manuscript.

References

  • [1] Marder SR, Organic nonlinear optical materials Where we have been and where we are going, Chemical Communications 2006;37;131-4.
  • [2] Mehkoom M, Afzal M, Ahmad S, Khan SA. The new pyrazoline derivative 5‐(3,4-Dimethoxy‐phenyl)‐3‐(2,5‐dimethyl‐thiophene‐3‐yl),‐4,5‐dihydro‐pyrazole‐1‐carbothioic acid amide (DDPA) as an advisable candidate for optical linearity, nonlinearity, and limiting performance. J Mol Liq 2022;345;117018.
  • [3] Gong P, Liu X, Kang L, Lin Z. Inorganic planar π-conjugated groups in nonlinear optical crystals: Review and Outlook. Inorganic Chemistry Frontiers 2020;7;839-852.
  • [4] Evans OR, Lin W. Crystal engineering of NLO materials based on metal-organic coordination networks. Ac Chem Res 2002; 35; 511–522.
  • [5] Abrinaei F, Kimiagar S, Gharedaghi S. Strong optical nonlinearity of CdS/nitrogen-doped reduced graphene oxide nanocomposites using Z-scan technique. Journal of Materials Science: Materials in Electronics 2018; 29; 2550–2560.
  • [6] Alamouti AF, Nadafan M, Dehghani Z, Ara MHM, Noghreiyan AV. Structural and Optical Coefficients Investigation of γ-Al2O3 Nanoparticles using Kramers-Kronig Relations and Z–scan Technique. Journal of Asian Ceramic Societies 2021; 9; 366–373.
  • [7] Dehghani Z, Nadafan M, Saievar IE. The effect of external applied fields on the third order nonlinear susceptibility of ferro-nematics. J Mol Liq 2015; 204; 70–75.
  • [8] Abrinaei F. Laser ablation of magnesium in water and investigation of optical nonlinearity by the Z-scan technique. Journal of the Optical Society of America B 2016; 33; 864.
  • [9] Hasmuddin M, Abdullah MM, Singh P, Shkir M, Vijayan N, Wahab MA. Ab-initio study of L-Tartaric Acid (LTA) single crystal for NLO application, Opt Laser Technol 2015; 74; 53–59.
  • [10] Jagadesan A, Sivakumar N, Mohan KR, Chakkaravarthi G, Arjunan S. Synthesis, crystal structure, growth and characterization of an optical organic material: 4-Aminopyridinium Trichloro acetate single crystal. Opt Mater 2018; 84; 864–869.
  • [11] Kwon SJ, Jazbinsek M, Kwon OP, Günter P. Crystal Growth and Morphology Control of OH1 Organic Electrooptic Crystals. Cryst Growth Des 2010; 10; 1552–1558.
  • [12] Sabaa MW, Elzanaty AM, Abdel-Gawad OF, Arafa EG. Synthesis, characterization and antimicrobial activity of Schiff bases modified chitosan-graft-poly(acrylonitrile). Int J Biol Macromol 2017; 109; 1280–1291.
  • [13] Poonia K, Siddiqui S, Arshad M, Kumar D. In vitro anticancer activities of Schiff base and its lanthanum complex. Spectrochim Acta A Mol Biomol Spectrosc 2016; 155; 146–154.
  • [14] Inan A, İkiz M, Tayhan SE, Bilgin S, Genç N. Antiproliferative, antioxidant, computational and electrochemical studies of new azo-containing Schiff base ruthenium(II) complexes. New Journal of Chemistry 2018; 42; 2952–2963.
  • [15] Leela S, Ramamurthi K, Bhagavannarayana G, Synthesis, growth, spectral, thermal, mechanical and optical properties of 4-chloro-4′dimethylamino-benzylidene aniline crystal: A third order nonlinear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2009; 74; 78–83.
  • [16] Leela S, Hema R, Stoeckli EH, Ramamurthi K, Bhagavannarayana G. Design, synthesis, growth and characterization of 4-methoxy-4′- dimethylamino-benzylidene aniline (MDMABA): A novel third order nonlinear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2010; 77; 927–932.
  • [17] Leela S, Deepa RT, Subashini A, Brindha S, Ramesh BR, Ramamurthi K. Studies on growth and characterization of nonlinear optical material 4-chloro-4′methoxy benzylideneaniline: A Schiff base organic material. Arabian Journal of Chemistry 2017; 10; S3974–S3981.
  • [18] Subashini A, Kumaravel R, Leela S, Evans HS, Sastikumar D, Ramamurthi K, Synthesis, growth and characterization of 4-bromo-4′chloro benzylidene aniline - A third order non linear optical material. Spectrochim Acta A Mol Biomol Spectrosc 2011; 78; 935–941.
  • [19] Subashini A, Bhagavannarayana G, Ramamurthi K. Synthesis, growth, optical, mechanical, dielectric and thermal properties of 4-chloro-4′-chlorobenzylidene aniline single crystal. Spectrochim Acta A Mol Biomol Spectrosc 2011; 82; 91–96.
  • [20] Czekalla GB. Elektronenuberfuhrung durch Lichtabsorption und-emission in Ele ktronen-Donator-Acceptor-Komplexen. Angewandte Chemie 1960;72;401-413.
  • [21] Shafiee A, Yahaya M.Determination of HOMO and LUMO of [6,6]-Phenyl C61-butyric Acid 3-ethylthiophene Ester and Poly (3-octyl-thiophene-2, 5-diyl) through Voltametry Characterization (Penentuan HOMO dan LUMO Asid [6,6]-Fenil C61-butirik Ester 3-etiltiofena dan Poli (3-oktil-tiiofena-2, 5-diyl) menerusi Pencirian Voltametri). Sains Malaysiana 2011; 40(2), 173-176.
  • [22] Runge E, Gross EKU. Density-Functional Theory for Time-Dependent Systems. Phys Rev Lett 1984; 52; 997–1000.
  • [23] Turkoglu G, Cinar ME, Buyruk A, Tekin E, Mucur SP, Kaya K, Ozturk T. Novel organoboron compounds derived from thieno[3,2-b] thiophene and triphenylamine units for OLED devices. J Mater Chem C Mater 2016; 4; 6045–6053.
  • [24] Wałęsa Chroab M, Tremblay MH, Skene WG. Hydrogen-Bond and Supramolecular-Contact Mediated Fluorescence Enhancement of Electrochromic Azomethines. Chemistry - A European Journal 2016; 22; 11382–11393.
  • [25] Salih KSM. Synthesis, characterization, surface analysis, optical activity and solvent effects on the electronic absorptions of Schiff base-functionalized amino thiophene derivatives: Experimental and TD-DFT investigations. J Mol Struct 2021; 1244;131267.
  • [26] Sıvrıkaya Y, Sakarya HC, Kiliç G, Ektı SF, Yandimoğlu M. New pyrene and fluorene-based π-conjugated Schiff bases: Theoretical and experimental investigation of optical properties. Journal of the Serbian Chemical Society 2024; 89; 1025–1038.
  • [27] Runge E, Gross EKU. Density-Functional Theory for Time-Dependent Systems. Physical Review Letters 1984;52;12.
  • [28] Becke AD. Density-functional thermochemistry. III. The role of exact Exchange. J Chem Phys 1993; 98; 5648–5652.
  • [29] Lee C, Yang W, Parr RG. Development of the Colic-Salvetti correlation-energy formula into a functional of the electron density. Phys Rev B 1988;37;785-789.
  • [30] Storm AT, Gjikaj M, Namyslo JC, Adams J, Schmidt A. 1,3-Thiazolium-4-aminides: Syntheses and Characterization of Fluorescent Mesoionic Compounds. European J Org Chem 2021; 34; 4803–4815.
  • [31] Cossi M, Rega N, Scalmani G, Barone V, Energies, Structures, and Electronic Properties of Molecules in Solution with the C-PCM Solvation Model. Comput Chem 2003;24;669-81.
  • [32] Barone V, Cossi M. Quantum Calculation of Molecular Energies and Energy Gradients in Solution by a Conductor Solvent Model. The Journal of Physical Chemistry A 1998;102;1995-2001.
  • [33] Underwood SJ, Douglas CJ. N-Pyridylimidates as Traceless Acyl Equivalents for Directed C-O Bond Functionalization. Organic Letters 2023;25;146-151.
  • [34] Lu T, Chen F. Multiwfn: A multifunctional wavefunction analyzer. J Comput Chem 2012; 33; 580–592.
  • [35] Humphrey W, Dalke A, Schulten K. VMD: Visual Molecular Dynamics. J Mol Graph 1996;1;33-8.
  • [36] Williams DJ, DS. Prasad PN. Introduction to Nonlinear Optical Effects in Molecules and Polymers. New York NY, USA;wiley; 1991.
  • [37] Vennila P, Govindaraju M, Venkatesh G, Kamal C. Molecular structure, vibrational spectral assignments (FT-IR and FT-RAMAN), NMR, NBO, HOMO-LUMO and NLO properties of O-methoxybenzaldehyde based on DFT calculations. J Mol Struct 2016; 1111; 151–156.
  • [38] Ergürhan O, Gürhan R, Parlak C, Alver Ö. Nonlinear Optical and Spectral Properties Of Hydroquinone & Fullerene Systems. Eskişehir Teknik Üniversitesi Bilim ve Teknoloji Dergisi B - Teorik Bilimler 2021; 9; 47–53.
  • [39] Abbaz T, Bendjeddou A, Villemin D. Structural and quantum chemical studies on aryl sulfonyl piperazine derivatives. Journal of Drug Delivery and Therapeutics 2019; 9; 88–97.
There are 39 citations in total.

Details

Primary Language English
Subjects Physical Organic Chemistry, Organic Chemical Synthesis
Journal Section Articles
Authors

Sultan Funda Ekti 0000-0001-6810-0030

Handan Can Sakarya 0000-0001-8174-1350

Yunuscan Sivrikaya 0000-0001-7158-3205

Project Number 202019059
Publication Date September 25, 2025
Submission Date February 3, 2025
Acceptance Date July 13, 2025
Published in Issue Year 2025 Volume: 26 Issue: 3

Cite

AMA Ekti SF, Can Sakarya H, Sivrikaya Y. AN EXPERIMENTAL–THEORETICAL INSIGHT INTO SYNTHESIS AND OPTICAL PROPERTIES OF STRUCTURALLY TUNED Π-CONJUGATED SCHIFF BASES. Estuscience - Se. September 2025;26(3):188-202. doi:10.18038/estubtda.1624326