Synthesis, spectral characterization and biological activities of Ag(I), Pt(IV) and Au(III) complexes with novel azo dye ligand (N,N,O) derived from 2-amino-6-methoxy benzothiazole

The novel ligand 2-[2'-(6-methoxybenzothiazolyl)azo]-3,5-dimethyl benzoic acid (6-MBTAMB), derived from 2-amino-6-methoxy benzothiazole, has been used to synthesize a series of new metal complexes of Ag(I), Pt(IV) and Au(III). The metal complexes were characterized by elemental analyses (CHNS), molar conductivity, crystal structure (XRD), spectroscopic techniques: FT-IR, 1H NMR, 13C NMR, UV-Vis, mass spectra, thermal analysis (TG-DTA), FE-SEM and magnetic properties. Results confirmed that the azo dye ligand behaves a tridentate and coordinates to the metal ion via nitrogen atom of azomethine group of heterocyclic benzothiazole ring, nitrogen atom of the azo group which is the farthest of the benzothiazole molecule and carboxylic oxygen. Antimicrobial properties of all newly synthesized azo compounds are also demonstrated against bacterial pathogenic organisms and fungi. These complexes are more effective against bacteria and less effective against fungi compared to standard antibacterial drugs (Novobiocin) and antifungal drugs (Cycloheximide). By using the DPPH (2,2-diphenyl-1-picrylhydrazyl) radical scavenging test, it was discovered that the complexes had good antioxidant properties. In addition, the (6-MBTAMB) and metal complexes were docked with the crystal structure of FGF Receptor 2 (FGFR2) kinase domain harboring the pathogenic gain of function K659E mutation identified in endometrial cancer using the Molecular Operating Environment module (MOE). In vitro studies on human endometrial cancer cell lines (MFE-296) as well as healthy human umbilical vein endothelial cells (HUVEC) show uptake of the intact compounds by the cancer cells and increased activity against the cancer cells.

Azo dyes containing 1,3,4-thiadiazole fragment: synthesis, properties

New 1,3,4-thiadiazole derivatives containing a diazenyl group, as well as simultaneously a diazenyl and an imino group were synthesized and their opticaland thermal properties were investigated. Initially, new azo compounds...

Highly efficient and simultaneous catalytic reduction of multiple toxic dyes and nitrophenols waste water using highly active bimetallic PdO–NiO nanocomposite

Azo dyes and nitrophenols have been widely used in the various industry which are highly toxic and affecting the photosynthetic cycle of aquatic organism. The industry disposals increase the accumulation of azo compounds in the environment. In the present study, we synthesized the low cost, PdO-doped NiO hetero-mixture via simple hydrothermal combined calcination process. The morphology results proved that, the spherical PdO nanoparticles are evenly doped with NiO nanoparticles. The band gap values of metal oxides NiO, PdO and PdO–NiO composite were found to be 4.05 eV, 3.84 eV and 4.24 eV, respectively. The high optical bandgap (Eg) value for composite suggests that the PdO interface and NiO interface are closely combined in the composite. The catalytic activity of the PdO–NiO was analyzed for the reduction of different toxic azo compounds namely, 4-nitrophenol (NP), 2,4-dinitrophenol (DNP), 2,4,6-trinitrophenol (TNP), methylene blue (MB), rhodamine B (RhB) and methyl orange (MO) separately and their mixture with the presence of a NaBH4. For the first time, the large volume of the toxic azo compounds was reduced into non-toxic compounds with high reduction rate. The proposed PdO–NiO catalyst exhibit excellent rate constant 0.1667, 0.0997, 0.0686 min−1 for NP, DNP and TNT and 0.099, 0.0416 and 0.0896 min−1 for MB, RhB and MO dyes respectively which is higher rate constant than the previously reported catalysts. Mainly, PdO–NiO completes the reduction of mixture of azo compounds within 8 min. Further, PdO–NiO exhibit stable reduction rate of azo compounds over five cycles with no significant loss. Hence, the proposed low cost and high efficient PdO–NiO catalyst could be the promising catalyst for degradation of azo compounds.

Synthesis, spectroscopic, and thermal studies of azo compounds from luminol and procaine with acetylacetone and their complexes

This The study entails the synthesis of two newly synthesized azo dyes luminol and procaine with acetylacetone (N1 and N2 correspondingly). Elementalanalysis, 1HNMR, T.G.A, and FTIR. have all been used to characterize dyes. These new dyes were reacted with Cpper and Nikel ionin 1:2 molar ratios to form of complexes of metals (II) with a general stoichiometry; CuL2, and NiL2 in complexes., FT IR, as well as the corresponding metal (II) complex, were used to characterize them. The dye acts as a bidentate ligand, according to elemental analysis and spectral results. The thermal properties of these compounds were investigated using thermogravimetric analysis (TGA). Thermal decomposition of these compounds is a process that occurs in stages.,

Coupling Reactions of Aryldiazonium Salt. Part-XI: Review on Coupling of Aryldiazonium Salts of Aminobenzothiazoles with Aromatic and Heterocyclic Components

The azo compounds synthesized from substituted 2-aminobenzothiazoles were scientifically significant for sensor, nano chemistry and pharmaceutically useful applications. Azo-dyes were very important and useful class of synthetic organic compounds, that have a huge variety of applications.

Novel Bis Maleimide Derivatives Containing Azo Group: Synthesis, Corrosion Inhibition, and Theoretical Study

Novel derivatives of heterocyclic azo compounds have been synthesized through a free catalyst reaction. The structures of the synthesized compounds were confirmed by using different techniques such as 1H-NMR, 13C-NMR, and mass spectroscopy. The prepared derivatives were evaluated as corrosion inhibitors for mild steel after the inhibitory performance toward mild steel in 0.1 M HCl solution. The prepared derivatives, i.e. (1,1'-(((1E,1'E)-1,4-Phenylenebis(diazene-2,1-diyl))bis(4-methyl-3,1-phenylene))bis(1H-pyrrole-2, 5-dione)) 1 and (1,1'-(((1Z,1'Z)-(Oxybis(4,1-phenylene))bis(diazene-2,1-diyl)) bis(4-methyl-3,1-phenylene))bis(1H-pyrrole-2,5-dione)) 2 showed inhibition efficiency 89.22% and 91.30%, respectively at concentration 1 × 10–3 M. The isotherm adsorptions of these derivatives were found to obey Langmuir model. Furthermore, Density functional theory was used for theoretical estimation of the HOMO, LUMO, and other chemical quantum parameters. The results indicated that the synthesized derivatives displayed a corrosive inhibitory property in which derivative 2 was more effective than derivative 1. In addition, the theoretical results were in agreement with the experimental data.

Determination of thymol with micellar extraction preconcentration

For the efficient preconcentration of azo compounds – products of the interaction of 4-nitrophenyldiazonium with thymol, a system 4-nitroaniline (4-NA) – NO2- – Triton X-100 – NaOH – ethanol has been proposed. The optimal conditions for the formation of micellarsaturated phases of the system under study have been established: 3.10-4 M 4-NA – 3.10-4 M NO2- – 5% Triton X-100 – 2.8 M NaOH – 10 vol. % С 2Н5ОН. A spectrophotometric study of the above system has been carried out. A linear dependence was built in the coordinates A (at λ max = 552 nm) vs с(thymol), which is described by an equation of the form A = f(c), A = 26291c + 0.02; R2 = 0.997. The range of the determined contents of thymol is (2·10-6 – 4·10-5) mol/l. A technique for the colorimetric determination of thymol in aqueous media (color channel G) has been developed. The intensity of the channel G chromaticity (IG) is linearly dependent on pc(thymol) in accordance with the equation IG = 54.2pc – 267, R 2 = 0; the lower limit of the determined contents of thymol is 1.10-6 mol/l, which is two times less than in the variant of its spectrophotometric determination. The profiles of petal diagrams in the color coordinates of the RGB CMYK model have been constructed; the dependences of their area (S) and perimeter (P) on the thymol concentration have been obtained (P: y = 278x – 10.13; R 2 = 0.97; S: y = 20182x – 87649, R 2 = 0.99).