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Abstract

Synthesis and Nonlinear Optical Studies of N-Containing Heterocyclic Compounds †

by
Maria Marinescu
1,*,
Maria Antonia Tănase
2,
Ludmila-Otilia Cinteză
2,*,
Ioana Cătălina Gȋfu
3,
Sabina Georgiana Burlacu
3 and
Cristian Petcu
3
1
Department of Organic Chemistry, Biochemistry and Catalysis, Faculty of Chemistry, University of Bucharest, 90-92 Sos Panduri, 050663 Bucharest, Romania
2
Department of Physical Chemistry, Bd. Regina, Faculty of Chemistry, University of Bucharest, Elisabeta 4-12, 0330018 Bucharest, Romania
3
National Institute for Research & Development in Chemistry and Petrochemistry, Splaiul Independenței 202, 060021 Bucharest, Romania
*
Authors to whom correspondence should be addressed.
Presented at the 17th International Symposium “Priorities of Chemistry for a Sustainable Development” PRIOCHEM, Bucharest, Romania, 27–29 October 2021.
Chem. Proc. 2022, 7(1), 39; https://doi.org/10.3390/chemproc2022007039
Published: 11 March 2022
Introduction: The organic compounds which contain a “push–pull” system, that means a couple donor (D)–acceptor (A) connected to a system which contributes to the delocalization of the π-electrons, define the classic structures with optical response due to large hyperpolarizabilities. These arise from a combination of strong electron donor groups (e.g., –NR2, –OR) and strong electron withdrawing groups (e.g., –NO2, –CN), positioned at opposite ends of a conjugated system [1,2] (Figure 1).
Materials and methods: Organic commercial and synthetic materials were used for the synthesis of the heterocyclic compounds. All compounds were characterized with physicochemical techniques (elemental analysis, 1H, 13C, FTIR, and UV-Vis spectroscopy). The SHG capability of samples was measured by using an experimental set-up [1,3].
Results: A series of N-containing heterocyclic compounds (benzimidazoles, benzothiazole pyrazolones, octahydroacridines) was synthesized and characterized [4,5,6,7,8,9]. The SHG (second harmonic generation) value was determined for each compound. The molecular polarizability (α), first order hyperpolarizabilities (βtot), dipole (μtot), and quadrupole (Q) moments, were calculated using DFT (density functional theory) method.
Conclusions: Our results highlight that the nonlinear optical (NLO) response of such small, twisted or flat molecules, mainly depends on the dihedral angles of aromatic and heteroaromatic rings toward the transmitter group. We also found that the electronical and structural peculiarities, of these compounds to be favorable for ultra-fast response times, i.e., femto seconds applications, as confirmed by our previous publications [2,5].

Author Contributions

Conceptualization, M.M. and L.-O.C.; methodology, M.M.; software, L.-O.C.; validation, M.M., L.-O.C. and C.P.; formal analysis, M.A.T.; investigation, I.C.G.; resources, S.G.B.; data curation, M.M.; writing—original draft preparation, M.M.; writing—review and editing, M.M.; visualization, L.-O.C.; supervision, M.M.; project administration, L.-O.C.; funding acquisition, M.M. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by a grant of the Ministry of Research, Innovation and Digitization CCCDI—UEFISCDI, project number PN-III-P2-2.1-PED-2019-3009, within PNCDI III.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

Not applicable.

Acknowledgments

The authors thank the Faculty of Chemistry for the necessary resources provided.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Matei, A.; Marinescu, M.; Constantinescu, C.; Ion, V.; Mitu, B.; Ionita, I.; Emandi, A.; Dinescu, M. Nonlinear optical studies on 4-(ferrocenylmethylimino)-2-hydroxy-benzoic acid thin films deposited by MAPLE. Appl. Surf. Sci. 2016, 374, 206–212. [Google Scholar] [CrossRef]
  2. Marinescu, M. Synthesis and nonlinear optical studies on organic compounds in laser deposited thin films. In Applied Surface Science; Injeti, G., Ed.; IntechOpen: Rijeka, Croatia, 2019; Chapter 1; pp. 1–26. ISBN 978-1-78984-098-8. [Google Scholar]
  3. Ion, V.; Matei, A.; Constantinescu, C.; Mitu, B.; Ionita, I.; Marinescu, M.; Dinescu, M.; Emandi, A. Octahydroacridine thin films grown by matrix-assisted pulsed laser evaporation for non linear optical applications. Mater. Sci. Semicond. Process. 2015, 36, 78–83. [Google Scholar] [CrossRef]
  4. Emandi, A.; Vasiliu, I.C.; Marinescu, M. Solvatochromic properties of azo pyrazolone ligands in coordinative compounds with erbium. Nanosci. Nanotechnol. Lett. 2013, 5, 487–492. [Google Scholar] [CrossRef]
  5. Marinescu, M.; Emandi, A.; Marton, G.; Cinteza, L.O.; Constantinescu, C. Structural studies and optical nonlinear response of some pyrazole-5-ones. Nanosci. Nanotechnol. Lett. 2015, 7, 846–854. [Google Scholar] [CrossRef]
  6. Potmischil, F.; Marinescu, M.; Loloiu, T. Hydroacridines XXVIII. Syntheses of New 9-Substituted 1,2,3,4,5,6,7,8-octahydroacridine Derivatives and their N(10)-Oxides. Rev. Chim. 2007, 58, 795–798. [Google Scholar]
  7. Marinescu, M.; Tablet, C.; Potmischil, F.; Hillebrand, M. Experimental and theoretical study of the interaction of 3-carboxy-5,6-benzocoumarin with some 1,2,3,4,5,6,7,8-octahydroacridines and the corresponding N-oxides. Spectrochim. Acta A 2011, 81, 560–569. [Google Scholar] [CrossRef] [PubMed]
  8. Potmischil, F.; Marinescu, M.; Nicolescu, A.; Deleanu, C. Hydroacridines: Part 30. 1H and 13C NMR spectra of 9-substituted 1,2,3,4,5,6,7,8-octahydroacridines and of their N-oxides. Magn. Res. Chem. 2009, 47, 1031–1035. [Google Scholar] [CrossRef] [PubMed]
  9. Potmischil, F.; Deleanu, C.; Marinescu, M.; Gheorghiu, D. Hydroacridines: Part 23. 1H and 13C NMR spectra of sym-octahydroacridine, its 9-(3-pyridyl) and 9-(4-pyridyl) derivatives and the corresponding N(10)-oxides. An experimental approach to the diamagnetic anisotropy of the pyridine nucleus. Magn. Res. Chem. 2002, 40, 237–240. [Google Scholar] [CrossRef]
Figure 1. Scheme of one organic compound with a “push–pull” system.
Figure 1. Scheme of one organic compound with a “push–pull” system.
Chemproc 07 00039 g001
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MDPI and ACS Style

Marinescu, M.; Tănase, M.A.; Cinteză, L.-O.; Gȋfu, I.C.; Burlacu, S.G.; Petcu, C. Synthesis and Nonlinear Optical Studies of N-Containing Heterocyclic Compounds. Chem. Proc. 2022, 7, 39. https://doi.org/10.3390/chemproc2022007039

AMA Style

Marinescu M, Tănase MA, Cinteză L-O, Gȋfu IC, Burlacu SG, Petcu C. Synthesis and Nonlinear Optical Studies of N-Containing Heterocyclic Compounds. Chemistry Proceedings. 2022; 7(1):39. https://doi.org/10.3390/chemproc2022007039

Chicago/Turabian Style

Marinescu, Maria, Maria Antonia Tănase, Ludmila-Otilia Cinteză, Ioana Cătălina Gȋfu, Sabina Georgiana Burlacu, and Cristian Petcu. 2022. "Synthesis and Nonlinear Optical Studies of N-Containing Heterocyclic Compounds" Chemistry Proceedings 7, no. 1: 39. https://doi.org/10.3390/chemproc2022007039

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