6-SULFO-2-NAFTOL ASOSIDA AZOBIRIKMALAR SINTEZI VA XOSSALARI
PDF

Keywords

6-sulfo-2-naftol, p-bromanilin, p-anizidin, p-xloranilin, p-nitroanilin, HPLC, IK, UB

How to Cite

6-SULFO-2-NAFTOL ASOSIDA AZOBIRIKMALAR SINTEZI VA XOSSALARI. (2026). Qo‘qon DPI. Ilmiy Xabarlar Jurnali, 8(3), 525-530. https://doi.org/10.70728/

Abstract

Mazkur ish 6-sulfo-2-naftol bilan turli aromatik aminlarning azobirikmalari sinteziga qaratilgan. Azobirikmalarning IK va UB spektr natijalari tahlil qilingan. Mahsulotlarning fizik kattaliklari orqali toutomer holatlar ifodalangan

PDF

References

[1] C. Graiff, «Structure and Properties of Organic Dyes in Solid State», Crystals, т. 10, вып. 11, с. 1021, ноя. 2020, doi: 10.3390/cryst10111021.

[2] G. Shabir и A. Saeed, «Synthesis of New Congo Red Derivative Dyes and their Application as Hardness Reduction in Hard Water.».

[3] K. K. Sharma, B. S. M. Rao, H. Mohan, J. P. Mittal, J. Oakes, и P. O’Neill, «Free-Radical-Induced Oxidation and Reduction of 1-Arylazo-2-naphthol Dyes: A Radiation Chemical Study», The Journal of Physical Chemistry A, т. 106, вып. 12, сс. 2915–2923, мар. 2002, doi: 10.1021/jp014025b.

[4] S. Suroj Rustamovich и Y. Muhabbat Razzoqberdievna, «SYNTHESIS AND PROPERTIES OF AZO COMPOUNDS BASED ON SOME AROMATIC AMINES WITH β-NAPHTHOL», AJT, сс. 25–29, сен. 2025, doi: 10.29013/AJT-25-7.8-25-29.

[5] H.-L. Wei, H.-J. Lu, Y.-H. Su, D.-T. Pan, и Z.-H. Luo, «Kinetic study on the solid–liquid diazo coupling reaction with time-varying viscosity», Chemical Engineering Science, т. 306, с. 121286, мар. 2025, doi: 10.1016/j.ces.2025.121286.

[6] A. V. Yatsenko, D. Yu. Kultin, и K. A. Paseshnichenko, «Solid-state induced tautomerism in some arylazo derivatives of resorcinol», Dyes and Pigments, т. 222, с. 111883, мар. 2024, doi: 10.1016/j.dyepig.2023.111883.

[7] J. J. F. Coen, A. T. Smith, L. P. Candeias, и J. Oakes, «New insights into mechanisms of dye degradation by one-electron oxidation processes», Journal of the Chemical Society, Perkin Transactions 2, вып. 11, сс. 2125–2129, ноя. 2001, doi: 10.1039/b105085k.

[8] H. C. Gardner, A. R. Kennedy, K. M. McCarney, E. Staunton, H. Stewart, и S. J. Teat, «Structures of five salt forms of disulfonated monoazo dyes», Acta Crystallogr C Struct Chem, т. 76, вып. 10, сс. 972–981, окт. 2020, doi: 10.1107/S2053229620012735.

[9] M. B. Kholboyeva и др., «Determination of FeIII) ion with a novel, highly efficient immobilized nitrosa R-salt in a polymer matrix», Chemical Review and Letters, т. 8, вып. 3, апр. 2025, doi: 10.22034/crl.2025.496212.1505.

[10] K. Bártová, I. Císařová, A. Lyčka, и M. Dračínský, «Tautomerism of azo dyes in the solid state studied by 15N, 14N, 13C and 1H NMR spectroscopy, X-ray diffraction and quantum-chemical calculations», Dyes and Pigments, т. 178, с. 108342, июл. 2020, doi: 10.1016/j.dyepig.2020.108342.

[11] M. U. Schmidt, J. Brüning, D. Wirth, и M. Bolte, «Two azo pigments based on β-naphthol», Acta Crystallogr C Cryst Struct Commun, т. 64, вып. 9, сс. o474–o477, сен. 2008, doi: 10.1107/S0108270108023421.

[12] T. Hihara, «Azo-hydrazone tautomerism of phenylazonaphthol sulfonates and their analysis using the semiempirical molecular orbital PM5 method», Dyes and Pigments, т. 59, вып. 1, сс. 25–41, окт. 2003, doi: 10.1016/S0143-7208(03)00093-7.

[13] G. R. Ferreira, H. C. Garcia, M. R. C. Couri, H. F. Dos Santos, и L. F. C. De Oliveira, «On the Azo/Hydrazo Equilibrium in Sudan I Azo Dye Derivatives», J. Phys. Chem. A, т. 117, вып. 3, сс. 642–649, янв. 2013, doi: 10.1021/jp310229h.

[14] A. R. Kennedy и др., «Monosulfonated Azo Dyes: A Crystallographic Study of the Molecular Structures of the Free Acid, Anionic and Dianionic Forms», Crystals, т. 10, вып. 8, с. 662, авг. 2020, doi: 10.3390/cryst10080662.

Creative Commons License

This work is licensed under a Creative Commons Attribution 4.0 International License.