Reactions catalyzed within inorganic and organic materials and at electrochemical interfaces commonly occur at high coverage and in condensed media, causing turnover rates to depend strongly on interfacial structure and composition, 82-76-8, Name is 8-(Phenylamino)naphthalene-1-sulfonic acid, SMILES is O=S(C1=C2C(NC3=CC=CC=C3)=CC=CC2=CC=C1)(O)=O, in an article , author is Hossaini, Zinatossadat, once mentioned of 82-76-8, Quality Control of 8-(Phenylamino)naphthalene-1-sulfonic acid.
ZnO/Ag/Fe3O4 nanoparticles supported on carbon nanotubes employing Petasites hybridus rhizome water extract: A novel organometallic nanocatalyst for the synthesis of new naphthyridines
In this study, ZnO/Ag/Fe3O4/CNTs nanoparticles (NPs) immobilized on carbon nanotubes (ZnO/Ag/Fe3O4/CNTs) were synthesized using Petasites hybridus rhizome water extract as a renewable, mild, and safe reducing agent and effective stabilizer without adding any surfactants. For the confirmation of the structure of the green synthesized NPs, various methods such as X-ray diffraction (XRD), FESEM, transmission electron microscopy (TEM), Energy-Dispersive X-Ray Spectroscopy (EDS), and Vibrating Sample Magnetometer (VSM) were employed. The ZnO/Ag/Fe3O4/CNTs magnetic NPs as a high performance catalyst was employed for the preparation of naphthyridine derivatives in high yields via the multicomponent reactions of phthalaldehyde, 2-aminoactonitrile, activated acetylenic compounds, alpha-haloketones, triphenyphophine, and ammonium acetate in aqueous media at ambient temperature. Due to having isoquinoline core, we investigate antioxidant property of some synthesized compounds by diphenyl-picrylhydrazine (DPPH) radical trapping and power of ferric reduction experiment. Furthermore, the disk diffusion test on Gram-positive and Gram-negative bacteria IS utilized for investigation of antimicrobial activity of some naphthyridines. The achieved outcomes of this experiment demonstrate that these synthesized compounds could prevent from growth of bacteria. Short time of reaction, high yields of product, easy separation of catalyst, and products are some benefits of this process.
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Reference:
1,8-Naphthyridine – Wikipedia,
,1,8-Naphthyridine | C8H6N2 – PubChem