Mononuclear nickel(II) and copper(II) coordination compounds with ligands based on acetyl(benzoyl)acetone S-methylisothiosemicarbazones and 8-quinolinecarboxaldehyde. Synthesis and crystal structure

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Аннотация

Template condensation of S-methylisothiosemicarbazones of acetyl- or benzoylacetone with 8-quinolinecarboxaldehyde in the presence of nickel(II) and copper(II) ions gave four new mononuclear coordination compounds [NiL1]I (I), [CuL1I] (II), [NiL2]I (III) и [CuL2I] (IV). The chemical composition of the products was confirmed by elemental analysis, IR spectroscopy, and mass spectrometry, and the crystal structure of compounds I and II was determined by X-ray diffraction analysis (CCDC no. 2266386, 2266387). X-ray diffraction study revealed a square planar coordination environment of the central ion of the cationic Ni(II) complex and square pyramidal geometry for the molecular Cu(II) complex.

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Авторлар туралы

M. Cocu

Moldova State University

Email: pavlina.bourosh@ifa.md

Institute of Chemistry

Молдавия, Chisinau

P. Bourosh

Moldova State University

Хат алмасуға жауапты Автор.
Email: pavlina.bourosh@ifa.md

Institute of Applied Physics

Молдавия, Chisinau

V. Kravtsov

Moldova State University

Email: pavlina.bourosh@ifa.md

Institute of Applied Physics

Молдавия, Chisinau

О. Danilescu

Moldova State University; Technical University of Moldova,

Email: pavlina.bourosh@ifa.md

Institute of Chemistry

Молдавия, Chisinau; Chisinau

I. Bulhac

Moldova State University

Email: pavlina.bourosh@ifa.md

Institute of Chemistry

Молдавия, Chisinau

Әдебиет тізімі

  1. Boulechfar Ch., Ferkous H., Delimi A. et al. // Inorg. Chem. Commun. 2023. V. 150. № 4. Р. 110451.
  2. Gerbeleu N.V., Arion V.B., Burges J. Template Synthesis of Macrocyclic Compounds. Wiley-VCH: Weinheim, 1999. 565 p.
  3. Graur V., Mardari A., Bourosh P. et al. // Acta Chim. Slov. 2023. V. 70. № 1. P. 122.
  4. Graur V., Usataia I., Bourosh P. et al. // Appl. Organomet. Chem. 2021. V. 35. № 5. P. e6172.
  5. Eram-Jamal S., Iqbal A., Abdul Rahman K., Tahmeena K. // J. Drug. Deliv. Ther. 2019. V. 9. P. 689.
  6. Devi J., Yadav M., Jindal D.K. et al. // Appl. Organometal. Chem. 2019. V. 33. P. 1.
  7. Ishak N.N.M., Jamsari J., Ismail A.Z. et al. // J. Mol. Struct. 2019. V. 1198. P. 126888.
  8. Zhang S., Dong J., Fan X. et al. // J. Coord. Chem. 2012. V. 65. P. 3098.
  9. Arion V.B. // Coord. Chem. Rev. 2019. V. 387. P. 348.
  10. Revenko M.D., Bourosh P.N., Stratulat E.F. et al. // Russ. J. Inorg. Chem. 2010. V. 55. № 9. P. 1387. https://doi.org/10.1134/S0036023610090093
  11. Bourosh P.N., Revenko M.D., Stratulat E.F. et al. // Russ. J. Inorg. Chem. 2014. V. 59. № 6. P. 545. https://doi.org/
  12. Liu Z.-Ch., Wang B.-D., Yang Zh.-Y. et al. // Eur. J. Med. Chem. 2009. V. 44. P. 4477.
  13. Hewawasam P., Fan W., Knipe J. et al. // Bioorg. Med. Chem. Lett. 2002. V. 12. P. 1779.
  14. Ukrainets I.V., Gorokhova V.O., Benzuglyi A.P., Sidorenko V.L. // Farm. Zh. 2000. V. 1. P. 75.
  15. Laverick R.J., Zhang N., Reid E. et al. // J. Coord. Chem. 2021. V. 74. P. 321.
  16. Revenko M.D., Bourosh P.N., Stratulat E.F. et al. // Russ. J. Inorg. Chem. 2009. V. 54. № 4. P. 530. https://doi.org/10.1134/S003602360904007X
  17. Stratulat E., Revenco M., Prisacari V. et al. // Analele ştiinţifice ale Universităţii de Stat din Moldova. Ser. Stiinte Chim. — Biol. 2006. P. 448.
  18. Revenko M.D., Prisakar′ V.I., Dizdar′ A.V. et al. // Khim.-Farm. Zh. 2011. V. 44. № 12. P. 40.
  19. Graur V., Chumakov Yu., Garbuz O. et al. // Bioinorg Chem Appl. 2022. Art. 2705332. https://doi.org/10.1155/2022/2705332
  20. Ablov A.V., Gerbeleu N.V., Oloi B.T. // Zh. Neorg. Khim. 1970. V. 15. № 10. P. 2705.
  21. Ablov A.V., Gerbeleu N.V., Oloi B.T. // Zh. Neorg. Khim. 1970. V. 15. № 11. P. 3114.
  22. Ablov A.V., Gerbeleu N.V., Oloi B.T. // Zh. Neorg. Khim. 1971. V. 16. № 1. P. 189.
  23. Caric S., Petrovic D., Lazar D., Leovac V. // Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem. 1978. V. 148. P. 153.
  24. Petrovic D., Ribar B., Caric S., Leovac V. // Z. Kristallogr., Kristallgeom., Kristallphys., Kristallchem. 1979. V. 150. P. 3.
  25. Cattelain E. // Bull. Soc. Chim. 1944. № 11. Р. 249.
  26. Gerbeleu N.V., Arion, V.V., Leovac V.M. et al. // J. Serb. Chem. Soc. 1992. № 57. P. 761.
  27. Leovac V.M., Jovanovic L.S., Cesljevicw V.I. et al. // Polyhedron. 1994. V. 13. P. 3005.
  28. Sheldrick G.M. // Acta Crystallogr. A. 2007. V. 64. P. 112.
  29. Sheldrick G.M. // Acta Crystallogr. C. 2015. V. 71. P. 3.
  30. Bellamy L.J. The Infrared Spectra of Complex Molecules. New York: Wiley, 1958.
  31. Gordon A., Ford R. The Chemist′s Companion: A Handbook of Practical Data, Techniques, and References. New York: Wiley, 1972.
  32. Nakanishi K. Infrared Absorption Spectroscopy. Tokyo: Holden-Day, 1963.
  33. Tarasevich B.N. IK spektry osnovnykh klassov organicheskikh soedinenii. Spravochnye materialy (IR Spectra of Main Classes of Organic Compounds. Reference Materials). Moscow: MGU, 2012.
  34. Nakamoto K. Infrared Spectra and Raman Spectra of Inorganic and Coordination Compounds. New York: Wiley, 1986.
  35. Koksharova E.V. // Visnik ONU. Khim. 2014. V. 19. № 2(50). Р. 27.

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Әрекет
1. JATS XML
2. Scheme 1. Synthesis of complexes I-IV.

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3. Fig. 1. Molecular structure of ionic complex I.

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4. Fig. 2. Fragment of the component packaging in I.

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5. Fig. 3. Molecular structure of complex II.

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6. Fig. 4. Fragment of the crystal structure II.

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