Skip to main content
Log in

SYNTHESIS AND CRYSTAL STRUCTURE OF THE Ni(II) COMPLEX WITH (4Z)-4-[(2-DIETHYLAMINOETHYLAMINO)METHYLENE]- 5-METHYL-2-PHENYLPYRAZOLE-3-ONE

  • Published:
Journal of Structural Chemistry Aims and scope Submit manuscript

Abstract

The Ni(II) complex based on (4Z)-4-[(2-diethylaminoethylamino)methylene]-5-methyl-2-phenylpyrazole-3-one (HL), being the condensation product of 5-hydroxy-3-methyl-1-phenylpyrazole-4-carbaldehyde with N,N-diethylethylenediamine, is synthesized. By the elemental analysis and IR spectroscopy it is found that the nickel complex has the composition Ni(L)CH3COO·CH3OH·H2O. The crystal and molecular structures of the complex are determined by single crystal Xray diffraction (XRD). From the XRD data it follows that the monochelate Ni(II) complex has a distorted octahedral structure due to bonds with a monodentate acetate anion and methanol and water molecules.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Scheme 1
Fig. 1
Fig. 2

Similar content being viewed by others

REFERENCES

  1. F. Marchetti, C. Pettinari, C. Di Nicola, A. Tombesi, and R. Pettinari. Coord. Chem. Rev., 2019, 401, 213069, DOI: 10.1016/j.ccr.2019.213069.

  2. F. Marchetti, C. Pettinari, and R. Pettinari. Coord. Chem. Rev., 2005, 249, 2909, DOI: 10.1016/j.ccr.2005.03.013.

  3. M. Cushman, M. Jayaraman, J. A. Vroman, A. K. Fukunaga, B. M. Fox, G. Kohlhagen, D. Strumberg, and Y. Pommier. J. Med. Chem., 2000, 43, 3665, DOI: 10.1021/jm000029d.

  4. Z.-G. Yu, W.-M. Ding, H.-R. Ji, and X.-Y. Zhu. Chin. J. Org. Chem., 2010, 30, 1358.

  5. K. L. Kees, J. J. Fitzgerald, K. E. Steiner, J. F. Mattes, B. Mihan, T. Tosi, D. Mondoro, and M. L. McCaleb. J. Med. Chem., 1996, 39, 3920, DOI: 10.1021/jm960444z.

  6. J. N. Asegbeloyin, O. T. Ujam, E. C. Okafor, I. Babahan, E. Poyrazoglu Coban, A. Özmen, and H. Biyik. Bioinorg. Chem. Appl., 2014, 2014, 718175, DOI: 10.1155/2014/718175.

  7. E. A. Bakr, G. B. Al-Hefnawy, M. K. Awad, H. H. Abd-Elatty, and M. S. Youssef. Appl. Organomet. Chem., 2018, 32, e4104, DOI: 10.1002/aoc.4104.

  8. R. Pettinari, F. Marchetti, C. Pettinari, A. Petrini, R. Scopelliti, C. M. Clavel, and P. J. Dyson. Inorg. Chem., 2014, 53, 13105, DOI: 10.1021/ic502274b.

  9. O. G. Idemudia, A. P. Sadimenko, and E. C. Hosten. Int. J. Mol. Sci., 2016, 17, 687, DOI: 10.3390/ijms17050687.

  10. O. G. Idemudia, A. P. Sadimenko, and A. J. Afolayan. Macromol. Symp., 2015, 351, 61, DOI: 10.1002/masy.201300128.

  11. J. N. Asegbeloyin, E. C. Okafor, N. N. Ukwueze, I. Babahan, and I. C. Agbo. Asian J. Chem., 2014, 26, 2753, DOI: 10.14233/ajchem.2014.16572.

  12. S. Sunitha and K. K. Aravindakshan Int. J. Pharm. Biomed. Sci., 2011, 2, 108.

  13. E. Pahontu, F. Julea, T. Rosu, V. Purcarea, Y. Chumakov, P. Petrenco, and A. Gulea. J. Cell Mol. Med., 2015, 19, 865, DOI: 10.1111/jcmm.12508.

  14. V. A. Joseph, J. H. Pandya, and R. N. Jadeja. J. Mol. Struct., 2015, 1081, 443, DOI: 10.1016/j.molstruc.2014.10.056.

  15. C. Deng, S. Abdurehman, L. Liu, D. Wu, D. Jia, and R. Zhou. Spectrochim. Acta, Part A, 2015, 148, 318, DOI: 10.1016/j.saa.2015.04.001.

  16. J. Guo, H. Yuan, D. Jia, M. Guo, and Y. Li. Spectrochim. Acta, Part A, 2017, 171, 149, DOI: 10.1016/j.saa.2016.07.052.

  17. H. Chai, G. Liu, L. Liu, and D. Jia. Spectrochim. Acta, Part A, 2005, 61, 2590, DOI: 10.1016/j.saa.2004.09.027.

  18. H. Liu, J. Guo, D. Jia, M. Guo, F. Le, L. Liu, D. Wu, and F. Li. J. Solid State Chem., 2014, 216, 73, DOI: 10.1016/j.jssc.2014.04.020.

  19. A. S. Burlov, V. G. Vlasenko, A. V. Dmitriev, V. V. Chesnokov, A. I. Uraev, D. A. Garnovskii, Y. V. Zubavichus, A. L. Trigub, I. S. Vasilchenko, D. A. Lypenko, E. I. Mal′tsev, T. V. Lifintseva, and G. S. Borodkin. Synth. Met., 2015, 203, 156, DOI: 10.1016/j.synthmet.2015.02.028.

  20. A. S. Burlov, Y. V. Koshchienko, N. I. Makarova, T. A. Kuz′menko, V. V. Chesnokov, M. A. Kiskin, S. A. Nikolaevskii, D. A. Garnovskii, A. I. Uraev, V. G. Vlasenko, and A. V. Metelitsa. Synth. Met., 2016, 220, 543, DOI: 10.1016/j.synthmet.2016.06.025.

  21. A. N. Gusev, M. A. Kiskin, E. V. Braga, M. Chapran, G. Wiosna-Salyga, G. V. Baryshnikov, V. A. Minaeva, B. F. Minaev, K. Ivaniuk, P. Stakhira, H. Ågren, and W. Linert. J. Phys. Chem. C, 2019, 123(18), 11850, DOI: 10.1021/acs.jpcc.9b02171.

  22. A. Gusev, V. Shul′gin, E. Braga, E. Zamnius, G. Starova, K. Lyssenko, I. Eremenko, and W. Linert. J. Lumin., 2018, 202, 370, DOI: 10.1016/j.jlumin.2018.05.077.

  23. A. N. Gusev, E. V. Braga, M. A. Kryukova, N. V. Lyubomirskii, E. A. Zamnius, and V. F. Shul′gin. Russ. J. Coord. Chem., 2020, 46, 251, DOI: 10.1134/S107032842004003X.

  24. B. A. Porai-Koshits and I. Ya. Kvitko. Zh. Obshch. Khim., 1962, 32, 4050.

  25. I. Ya. Kvitko and B. A. Porai-Koshits. Zh. Org. Khim., 1964, 34, 3005.

  26. Bruker, APEX3. Bruker AXS: Madison, WI, 2018.

  27. Bruker, SADABS, Bruker/Siemens Area Detector Absorption Correction Program. Bruker AXS: Madison, WI, 2016.

  28. G. M. Sheldrick. Acta Crystallogr., Sect. C, 2015, 71, 3, DOI: 10.1107/S2053229614024218.

  29. D. A. Garnovskii, A. S. Antsyshkina, N. I. Makarova, V. G. Vlasenko, A. V. Churakov, G. G. Sadikov, V. S. Sergienko, Y. V. Zubavichus, S. I. Levchenkov, A. I. Uraev, and A. S. Burlov. Russ. J. Inorg. Chem., 2015, 60(12), 1528, DOI: 10.1134/S0036023615120116.

  30. A. S. Burlov, A. S. Antsyshkina, G. G. Sadikov, V. S. Sergienko, A. I. Uraev, E. V. Korshunova, D. A. Garnovskii, T. V. Lifintseva, G. S. Borodkin, A. G. Ponomarenko, G. G. Chigarenko, and I. L. Eremenko. Russ. J. Gen. Chem., 2012, 82, 1846, DOI: 10.1134/S1070363212110217.

  31. D. A. Garnovskii, A. S. Antsyshkina, A. V. Churakov, G. G. Sadikov, V. S. Sergienko, I. S. Vasil′chenko, A. I. Uraev, V. G. Vlasenko, Ya. V. Zubavichus, S. I. Levchenkov, Yu. V. Revinskii, and A. S. Burlov. Russ. J. Inorg. Chem., 2014, 59, 431, DOI: 10.1134/S0036023614050088.

  32. A. S. Morkovnik, L. N. Divaeva, A. I. Uraev, R. K. Mamin, I. G. Borodkina, G. S. Borodkin, A. S. Burlov, A. D. Garnovskii, and K. A. Lyssenko. Russ. Chem. Bull., 2008, 57, 1496, DOI: 10.1007/s11172-008-0194-5.

  33. N. I. Rtishchev, A. V. Elcov, I. Ya. Kvitko, and L. V. Alaam. Zh. Obshch. Khim., 1980, 50, 2070.

  34. A. I. Uraev, K. A. Lyssenko, V. G. Vlasenko, Ya. V. Zubavichus, M. P. Bubnov, N. I. Makarova, D. A. Garnovskii, and A. S. Burlov. Polyhedron, 2018, 146, 1, DOI: 10.1016/j.poly.2018.02.018.

  35. V. Vlasenko, D. Garnovskii, G. Aleksandrov, N. Makarova, S. Levchenkov, A. Trigub; Y. Zubavichus, A. Uraev, Y. Koshchienko, and A. Burlov. Polyhedron, 2019, 157, 6, DOI: 10.1016/j.poly.2018.09.065.

Download references

Funding

The study was supported by the Ministry of Science and Higher Education of the Russian Federation (State Task in the Scientific Activity Area at the Southern Federal University, 2020) and RUDN Program “5-100”.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to A. S. Burlov.

Ethics declarations

The authors declare that they have no conflict of interests.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Burlov, A.S., Vlasenko, V.G., Koshchienko, Y.V. et al. SYNTHESIS AND CRYSTAL STRUCTURE OF THE Ni(II) COMPLEX WITH (4Z)-4-[(2-DIETHYLAMINOETHYLAMINO)METHYLENE]- 5-METHYL-2-PHENYLPYRAZOLE-3-ONE. J Struct Chem 61, 1599–1605 (2020). https://doi.org/10.1134/S0022476620100121

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1134/S0022476620100121

Keywords

Navigation