{[Cu(C₆H₈N₂O₂S)(C₃H₇NO)](NO₃)} TARKIBLI ARALASH-LIGANDLI POLIMER KOMPLEKS BIRIKMASINING MOLEKULYAR VA KRISTALL TUZILISHI
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Keywords

copper(II) complex
sulfanilamide
dimethylformamide
polymeric complex
crystal structure
X-ray diffraction
coordination chemistry
octahedral geometry
hydrogen bonding
SHELXL.

How to Cite

{[Cu(C₆H₈N₂O₂S)(C₃H₇NO)](NO₃)} TARKIBLI ARALASH-LIGANDLI POLIMER KOMPLEKS BIRIKMASINING MOLEKULYAR VA KRISTALL TUZILISHI. (2026). Qo‘qon DPI. Ilmiy Xabarlar Jurnali, 8(6), 36-42. https://doi.org/10.70728/a.series.tab.v08.i06.006

Abstract

Ushbu maqolada sulfanilamid (4-aminobenzoysulfanilamid) va dimetilformamid (DMFA) ligandlari asosida sintez qilingan mis(II) ning aralash-ligandli polimer kompleks birikmasining — {[Cu(C₆H₈N₂O₂S)(C₃H₇NO)](NO₃)} — rentgen- kristallografik tadqiqi natijalari bayon etiladi. Birikmaning monoklinik kristall tizimiga mansub ekanligi, P2₁/c fazoviy guruhida (a = 9.0138(8) Å, b = 14.5605(8) Å, c = 11.4428(9) Å, β = 109.237(9)°, V = 1418.0(2) ų, Z = 6) kristallanishi aniqlandi. Mis(II) atomi oltita ligand bilan koordinatsiya hosil qilib, buzilgan oktaedrik geometriyani tashkil etadi. Ligandlar sulfanilamid va dimetilformamid boʻlgan holda mis markazi bilan koordinatsion bogʻlar orqali bogʻlangan. Vodorod bogʻlanishlari va π–π oʻxshash oʻaro taʼsirlashuvlar kristall panjarasining barqarorligini taʼminlaydi. Rentgen-difraktsion maʼumotlarning qayta ishlash natijalari quyidagicha: R1 = 0.0853 (I > 2σ(I)), wR2 = 0.2344 (barcha maʼumotlar). Maqolada birikmaning geometrik parametrlari, bogʻ uzunliklari va burchaklari batafsil muhokama qilinadi. Kalit soʻvzlar: mis(II) kompleksi, sulfanilamid, dimetilformamid, polimer kompleks, kristall tuzilishi, rentgen-difraktsiya, koordinatsion kimyo, oktaedrik geometriya, vodorod bogʻlanishi, SHELXL.
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References

1. Groom C.R., Bruno I.J., Lightfoot M.P., Ward S.C. The Cambridge Structural Database // Acta Crystallogr. B. – 2016. – Vol. 72. – P. 171–179.

2. Garoufis A., Hadjikakou S.K., Hadjiliadis N. Bioinorganic chemistry of nickel and its coordination compounds with amino acids and peptides // Coord. Chem. Rev. – 2009. – Vol. 253. – P. 1384–1397.

3. Keri R.S., Bannur S.V. Biological activity of sulfonamides // Bioorg. Med. Chem. – 2015. – Vol. 23. – P. 6087–6095.

4. Cotton F.A., Wilkinson G., Murillo C.A., Bochmann M. Advanced Inorganic Chemistry. – 6th ed. – New York: Wiley-Interscience, 1999. – 1355 p.

5. ugli Mamatsabirov, F. O., Ibragimov, B. T., Normamatov, A. S., Kamolov, S. N., ugli Mambetov, A. B., Hamro, M., ... & Ibragimov, A. B. (2026). The structure and biological activity of 3-amino-4-methyl benzoic acid and its supramolecular compound with nickel triethanolamine complex. Inorganic Chemistry Communications, 116598.

6. Zaltariov M.F., Shishkin O.V., Shishkina S.V. et al. Crystal structure and properties of copper(II) complexes with sulfonamides // Dalton Trans. – 2016. – Vol. 45. – P. 14559–14569.

7. Biradha K., Su C.Y., Vittal J.J. Recent developments in crystal engineering // Cryst. Growth Des. – 2011. – Vol. 11. – P. 875–886.

8. Addison A.W., Rao T.N., Reedijk J. et al. Synthesis, structure and spectroscopic properties of copper(II) complexes containing nitrogen-sulphur donor ligands // J. Chem. Soc. Dalton Trans. – 1984. – P. 1349–1356.

9. Sheldrick G.M. Crystal structure refinement with SHELXL // Acta Crystallogr. C. – 2015. – Vol. 71. – P. 3–8.

10. Dolomanov O.V., Bourhis L.J., Gildea R.J., Howard J.A.K., Puschmann H. OLEX2: a complete structure solution, refinement and analysis program // J. Appl. Cryst. – 2009. – Vol. 42. – P. 339–341.

11. Sheldrick G.M. SHELXT – Integrated space-group and crystal-structure determination // Acta Crystallogr. A. – 2015. – Vol. 71. – P. 3–8.

12. Bernstein J. Polymorphism in Molecular Crystals. – Oxford: Clarendon Press, 2002. – 410 p.