Synthesis, Characterization and Analytical Study of New Azo Dye
DOI:
https://doi.org/10.56714/bjrs.48.1.6Keywords:
Azo dyes,, indicators, ionization and protonation constants, solvent effectAbstract
The azo dye ((E)-4-((4-aminophenyl) diazenyl) naphthalen-1-ol) was prepared by diazotization and coupling reaction with 1-naphthol. The azo dye was diagnosed by FT-IR, 1H-NMR, mass spectra and visible spectrometry. The acid and basic properties were studied by the visible absorption spectra of the dye at different pH values and appearance of a clear isobestic point and a high absorption peak at the maximum wavelength (595nm) which is due to the absorption of the negative formula of the dye in the basic medium and an absorption peak at the wavelength (477nm) that is due to the absorption of the proton formula of the dye in the acidic medium. The ionization and protonation constants were calculated and the extent of the indicator within pH (7.4 - 9.4). The effect of the solvents on the visible absorption spectra of the dye was studied, and a clear red shift of the dye spectra was observed in the polar solvents.
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R. M. Abdul, R . M. Usman, T. H. Bokhari, A. ul Haq , M. Saeed , A. Rahman , M. Siddiq, A. Rasheed, M. UnNisa, J. Mol. Liq 301(1), 112408 (2020).
S. Benkhaya, S. M. Rabet, A. El Harf, Inorg. Chem. Commu 115, 107891 (2020).
S. Benkhaya, S. M. rabet, A. El Harfi, Heliyon 6, 1, (2020).
V. Selvaraj, T. Swarna Karthika, C. Mansiya, M. Alagar, J. Mol. Struc 1224(15), 129195 (2021).
T. A. Fahad, A. A. Ali, A. H. Baty, W. J. Pharmaceutical Res 8, 2 (2019).
M. Albasha , Int. J. Acade. Sci. Res 6(4), 16 (2018).
L. A. AL-Rubaie, R. J. Mhessn, E-J. Chem 9(1), 465 (2012).
S. Benkhaya, S. El Harfi, A. El Harfi, appl. J. enviro. Eng. Sci 13, 311 (2017).
D. Chomicki, O. Kharchenko, L . Skowronski, J. Kowalonek, A. Kozanecka-Szmigiel, D. Szmigiel, V. Smokal, O. Krupka, B. Derkowska-Zielinska, Int. J. Mol. Sci 21, 5755 (2020).
G. Prashantha, R. A. Shoukat Ali, J. Keshavayya, P. Kamaraj, P.A.Vivekanand, J. Uni. Shanghai for Sci. and Tech 22, 12 (2020).
M. El-Mahalawy, M.M. Abdou, A. R. Wassel, Na. Cen. Bio. Inf 248, 119243 (2021).
L. H. Madkour, S. Kaya, C. Kaya, L. Guo, J. Taiwan Instit. Chem. Eng 68, 461(2016).
N. M. Aljamali, Biochem. & Analy. Biochem 4(2), 1 (2015).
A. Ali, L. A. Rusin, Asian J. Res.Chem. and Pharm. Sci 4(1), 11(2016).
A. Ali, L. A. Rusin , Res. J. Pharm., Bio. and Chem. Sci 7(1), 1921 (2016).
H. Sh. Mohammed, A. M. Yasir, Int. J. Adv. Res 5(5), 164 (2016).
V. G. Vidya, V. Sadasivan, Asian J. Chem 30(9), 2049 (2018).
D. Canakci, Sci. Rep 10, 477 (2020).
M. N. Matadaa , K. Jathi, P. Malingappa, I. Pushpavathi , Chem. Data Coll. 25, 100314 (2020).
A. Ali, M. Kh. Hamza, J.Thi-Qar Sci 4(3), (2014).
A. Ali, Ibn Al-Haitham J. Pure & Appl. Sci 27(1), (2014).
H. Rashidnejad, M. Ramez, N. N. Pesyan, P. J. Mahon, M. M. M. Raposo, P. J. Coelho, A. Ng Kay Lup, A. Soltani , J. Mol. Struc 1223, 129323 (2021).
A. Ali, T. A. Fahad, W. A. Abdullah, J. Kufa Chem. Sci 12(8), 2 (2013).
T. A. Fahad, A. A. Ali, H. K. Ebraheem, Basrah J. Sci 32(1), 1 (2014).
A. Ali, H. A. Alstar , J. Basrah Res. ((Sci.)) 22(39), 1 (2013).
J. Zia , G. Mancinia , M. Bustreoc , A. Zycha , R. Donnod , A. Athanassioua and D. Fragoulia, Chem. Eng. J 403, 126373 (2021).
R. H. Fayadh, A. A. Ali, F. M. Al -Jabri , Inte. J. Eng. and Tech. Res 3, 3 (2015).

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