Synthesis, Characterization, and Analytical Applications of o-Substituted Benzoic Acid Chelating Resin
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چکیده
منابع مشابه
Selective Sorption of Heavy Metal Ions from Aqueous Solutions Using m-Cresol Based Chelating Resin and Its Analytical Applications
Salicylic acid-Formaldehyde-m-Cresol (SFM) terpolymer had been synthesized in DMF media by conventional method. The resulting resin had been characterized by FTIR spectra, elemental and thermogravimetric analyses. The morphology of SFM resin had been studied by SEM and Optical photograph. Various parameters like rate of equilibration, effect of pH on ion exchange capacity and effect of conc...
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Cr(III), Co(II), Ni(II), Cu(II) and Zn(II) salts of 2-(4-nitrophenylaminocarbonyl)benzoic acid were characterized by physical, analytical and spectroscopic studies and checked for their in-vitro antimicrobial activity against three bacterial strains, Mycobacterium smegmatis (Gram +ve), Escherichia coli (Gram -ve), Pseudomonas aeuroginosa (Gram -ve) and three fung...
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Hammett constants (σ) can be important factor to understanding substitution and position effects on benzoic acid. This report describes a computational study of ∆G◦ and σ for six substituted benzoic acid (X= F,Cl ,OH ,NH2 ,CN,NO2 )and phenylacetic acid substituted (X=OH ,NH2 ) at para and meta positions ingas and aqueousphases by DFT method and comparesit to available experimental and theoretic...
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Several cycline dependent kinase 2 (CDK2) inhibitors with different chemical structures have been introduced. The hinge region of CDK2 (residues 81–84) contains a set of hydrogen bond donor and acceptor sites some of which must be satisfied for potent inhibitor binding. The benzimidazolone skeleton may provide such interactions. Accordingly, 3-sulfonamide substituted benzamido-benzimidazolones ...
متن کاملSynthesis and Primary Cytotoxic Screening of Some 3- Sulfonamide Substituted Benzamido-benzimidazolones
Several cycline dependent kinase 2 (CDK2) inhibitors with different chemical structures have been introduced. The hinge region of CDK2 (residues 81–84) contains a set of hydrogen bond donor and acceptor sites some of which must be satisfied for potent inhibitor binding. The benzimidazolone skeleton may provide such interactions. Accordingly, 3-sulfonamide substituted benzamido-benzimidazolones ...
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