KOBALT(II)NING 7-YODO-8-GIDROKSIXINOLIN-5-SULFOKISLOTA (FERRON) BILAN KOMPLEKS BIRIKMASINING SINTEZI VA IQ- SPEKTROSKOPIK TADQIQI
PDF

Keywords

Ferron
7-yodo-8-gidroksixinolin-5-sulfokislota
kobalt(II)
koordinatsion birikma
IQ- spektroskopiya
O
N-xelat
sulfonat
metal ioni. 1.

How to Cite

KOBALT(II)NING 7-YODO-8-GIDROKSIXINOLIN-5-SULFOKISLOTA (FERRON) BILAN KOMPLEKS BIRIKMASINING SINTEZI VA IQ- SPEKTROSKOPIK TADQIQI. (2026). Qo‘qon DPI. Ilmiy Xabarlar Jurnali, 8(9), 919-925. https://doi.org/10.70728/a.series.tab.v08.i09.120

Abstract

Mazkur maqolada 7-yodo-8-gidroksixinolin-5-sulfokislota (Ferron, C₉H₆INO₄S) va kobalt(II) xlorid geksagidrat (CoCl₂·6H₂O) o‘rtasidagi kompleks hosil bo‘lish jarayoni tadqiq qilindi. Ferron suv–etanol (1:1) aralashmasida eritilib, CoCl₂·6H₂O eritmasi bilan pH 5,5 muhitda reaksiyaga kiritildi. Reaksiya aralashmasini 40,5 °C da quritish pechida sekin bug‘latish usulida 14–17 kun davomida bug’latildi natijada och pushti rangli, kubsimon shaklli kristallar olindi; reaksiya unumi 77,3 % ni tashkil qildi. Organik ligand va olingan kompleksning 4000–600 sm⁻¹ diapazondagi IQ spektrlari solishtirildi. Spektrogrammalardagi aniq pik qiymatlari asosida xinolin halqasining C=N va C=C sohasidagi siljishlar, fenolik C–O tebranishlarining o‘zgarishi hamda kompleksda suvga xos keng O–H yutilishining paydo bo‘lishi aniqlandi. Ushbu o‘zgarishlar Ferronning Co(II) markaziga O,N-donor atomlari orqali koordinatsiyalanishi haqidagi taxminni qo‘llab- quvvatlaydi. SO₃⁻ guruhining 1042 sm⁻¹ atrofidagi signali deyarli saqlanib qolganligi sababli uning koordinatsiyadagi ishtiroki IQ ma’lumotlari bilan qat’iy tasdiqlanmadi. Kompleksning taxminiy tarkibi [Co(Ferron)₂(H₂O)₂] modeli sifatida taklif qilishim mumkin.
PDF

References

1. Prachayasittikul V., Prachayasittikul S., Ruchirawat S., Prachayasittikul V. 8- Hydroxyquinolines: a review of their metal chelating properties and medicinal applications. Drug Design, Development and Therapy. 2013;7:1157–1178. DOI: 10.2147/DDDT.S49763.

2. Yoe J.H. 7-Iodo-8-hydroxyquinoline-5-sulfonic acid as a reagent for the colorimetric determination of ferric iron. Journal of the American Chemical Society. 1932;54(11):4139–4143. DOI: 10.1021/ja01350a002.

3. Musha S., Ogawa K. Ferron as an indicator in complexometric titration of Fe(III). Bunseki Kagaku. 1959;8(3):161–166. DOI: 10.2116/bunsekikagaku.8.161.

4. Davenport W.H. The determination of aluminum in the presence of iron. Analytical Chemistry. 1949;21:710–711.

5. Nakamoto K. Infrared and Raman Spectra of Inorganic and Coordination Compounds. Part B. 6th ed. Hoboken: Wiley; 2009.

6. Socrates G. Infrared and Raman Characteristic Group Frequencies: Tables and Charts. 3rd ed. Chichester: Wiley; 2001.

7. Zhang F., Li Y.-Z., Gao X., Chen H.-L., Liu Q.-T., Odani A., Yamauchi O. Aromatic Iodine-Assisted Self-assembly of a Cobalt(II) Complex of Ferron. Chemistry Letters. 2004;33(5):556–557. DOI: 10.1246/cl.2004.556.

8. PubChem. Ferron (8-hydroxy-7-iodo-5-quinolinesulfonic acid), CID 11043. Molecular formula C₉H₆INO₄S; molecular weight 351.12 g/mol; CAS 547-91-1.

9. Musha S., Ogawa K. Complex formation of ferric iron with 7-iodo-8- hydroxyquinoline-5-sulfonic acid (Ferron). Journal of Coordination Chemistry. 1959.

10. Storm Å.R., Pedersen B., Theander O., Brimacombe J.S., Cook M.C. Stability of Metal Chelates of Co(II), Ni(II), Mn(II), and Zn(II) with 7-Iodo-8-hydroxyquinoline-5- sulphonic Acid (Ferron). Acta Chemica Scandinavica. DOI:

11. 3891/acta.chem.scand.17-0667.

12. González-Baró A.C., Baran E.J. Synthesis and spectroscopic behavior of some oxovanadium complexes of 7-iodo-8-hydroxyquinoline-5-sulfonate. Journal of the Brazilian Chemical Society. 2001;12(2):208–214. DOI: 10.1590/S0103-50532001000200014.

13. Baskar Raj S., et al. Metal-binding modes in sulfoxines: supramolecular network in (8-hydroxyquinoline-5-sulfonato-N,O)sodium(I). Acta Crystallographica Section 2002;58:m513–m516.

14. Zhu X., Zhang H., Zhou Y., Guan L. Hydrothermal synthesis, crystal structure, and magnetic properties of coordination polymers containing 7-iodo-8-hydroxyquinoline-5- sulfonic acid. Zeitschrift für anorganische und allgemeine Chemie. 2010;636:457–461. DOI:

15. 1002/zaac.200900347.

16. Balasubramani K., Thomas Muthiah P., Bocelli G., Cantoni A. Synthesis and crystal structure of mercury(II) chloride–ferron adduct. Journal of Coordination Chemistry.