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Item Spectrophotometric determination of palladium(II) using piperonal thiosemicarbazone(2003) Shetty, P.; Nityananda, Shetty, A.; Gadag, R.V.A simple, rapid, selective and sensitive spectrophotometric method for the determination of palladium is proposed using piperonal thiosemicarbazone (PATS) as a reagent. The reagent forms a 1:2 complex (Pd:Reagent) with palladium. The yellow complex is soluble in 32-40% ethanol and has an absorption maximum at 363 nm. Beer's law is obeyed upto 3.85 ppm of palladium and the optimum concentration range is 0.5-2.45 ppm of Pd. The molar absorptivity and Sandell's sensitivity are 3. 80 x 104 dm3 mol-1 cm -1 and 2.8 x 10-3 ?g cm-2, respectively. The experimental conditions for complete colour development and the interference from various ions are investigated. The method is used for the determination of palladium in its complexes and synthetic mixtures.Item Thioacetamide as a releasing agent for the complexometric determination of thallium(iii) in its synthetic alloys and complexes(2007) Karthikeyan, J.; Parameshwara, P.; Nityananda, Shetty, A.; Shetty, P.A simple and selective complexometric method for the determination of thallium is proposed, based on the masking ability of thioacetamide towards thallium(III). Thallium present in a given sample solution is first complexed with a known excess of EDTA and the surplus EDTA is titrated with standard zinc sulphate solution at pH 5-6 (hexamine buffer) using xylenol orange as the indicator. A 0.8% aqueous solution of thioacetamide is then added to displace EDTA from the TI(III)-EDTA complex. The released EDTA is titrated with standard zinc sulphate solution as before. Reproducible and accurate results are obtained for 0.018 - 0.371 mol L-1(3.79mg - 75.91mg) of Tl(III) with relative error less than 0.43% and coefficient of variation not more than 0.26%. The interference of various ions was studied and the method was used for the analysis of thallium in its synthetic alloy mixtures and also in complexes.Item The inhibition action of ethyl-2-phenyl hydrozono-3-oxobutyrate on the corrosion of 6061 Al alloy/SiCp composite in hydrochloric acid medium(2010) Kini, U.A.; Shetty, P.; Shetty, S.D.; Isloor, A.M.; Herle, R.The inhibition behavior of ethyl-2-phenyl hydrozono-3-oxobutyrate on the corrosion of 6061 Al alloy/SiCp composite in 0.1, 0.5 and 1 N hydrochloric acid solution at four different temperatures (30-60 C) has been investigated using potentiostatic polarization techniques and weight loss method. The results indicated that the corrosion inhibition efficiency and the extent of surface coverage were increased with the increase in inhibitor concentration up to a critical concentration. The adsorption of the inhibitor compound on the composite surface was found to obey Temkins' and Langmuir adsorption isotherms. The potentiostatic polarization results have revealed that oxobutyrate acts as an efficient cathodic inhibitor for the corrosion of 6061 Al alloy/SiCp composite in HCl medium. The thermodynamic parameters for the corrosion and adsorption processes were determined. 2010.Item The inhibition action of N-furfuryl-N?-phenyl thiourea on the corrosion of mild steel in acid media(2006) Shetty, S.D.; Shetty, P.; Nayak, H.V.S.The inhibiting effect of N-furfuryl-N?-phenyl thiourea (FPTU) on the corrosion of mild steel in aqueous solutions of 0.05 and 0.1MHCl, as well as 0.025 and 0.05 M H2SO4 has been demonstrated using the potentiodynamic polarization technique. The polarization data showed that FPTU acts as an efficient anodic inhibitor for mild steel in both acid solutions. Avery high inhibition efficiency was evidenced in both acid solutions and it was found to vary with the concentration of the inhibitor and temperature. The obtained kinetic parameters of adsorption revealed spontaneous adsorption and a strong interaction of FPTU with the mild steel surface.Item T3P mediated synthesis of some new quinoline substituted pyrazole derivatives and its antibacterial studies(2012) Chandrakantha, B.; Isloor, A.M.; Peethambar, S.K.; Shetty, P.A series of new N-(substituted)-5-phenyl-1-(quinolin-2-yl)-1H-pyrazole-4-carboxamide derivatives (5a-h) have been synthesized by condensing ethyl-3-(dimethylamino)-2-[(phenyl)carbonyl]prop-2-enoate 2 with quinoline-2-yl-hydrazine. Compound 3 is hydrolyzed into 4 which is upon further coupled with different aromatic/aliphatic amines using 50% prpopyl phosphonic anhydride (T3P) in ethyl acetate as coupling reagent to afford different quinoline substituted pyrazole carboxamide derivatives. All the newly synthesized compounds were screened for their invitro antibacterial studies against Escherichia coli, Bacillus subtilis and Pseudomonas aeruginosa. The results revealed that compounds 5d, 5f, and 5h showed good antibacterial activity towards all bacterial strains. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral study and also by C, H, N analyses.Item Synthesis, characterization and biological activity of some new 1,3,4-oxadiazole bearing 2-flouro-4-methoxy phenyl moiety(2010) Chandrakantha, B.; Shetty, P.; Nambiyar, V.; Isloor, N.; Isloor, A.M.In the present study a series of new 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy moiety were synthesized. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral study and also by C, H, N analyses. All the newly synthesized compounds were screened for their antibacterial and antifungal studies. Antimicrobial studies revealed that compounds 4a and 4b showed significant antibacterial activity against Escherichia coli and Pseudomonas aeruginosa Compound 4i showed significant antifungal activity against C. albicans. 2009 Elsevier Masson SAS. All rights reserved.Item Synthesis, characterization and antimicrobial activity of novel ethyl 1-(N-substituted)-5-phenyl-1H-pyrazole-4-carboxylate derivatives(2012) Chandrakantha, B.; Isloor, A.M.; Shetty, P.; Isloor, S.; Malladi, S.; Fun, H.K.In the present study, a novel series of Pyrazole derivatives (3a-m) were synthesized by condensing ethyl-3-(dimethylamino)-2-(phenylcarbonyl)prop-2- enoate with different aromatic and aliphatic hydrazines. These newly synthesized compounds were characterized by NMR, mass spectral, IR spectral studies as well as by C, H, and N analyses. All the newly synthesized compounds were screened for their antibacterial properties against Staphylococcus aureus, Bacillus subtilis, Escherichia coli, and Pseudomonas aeruginosa. Among the screened samples, 3c, 3f, 3k, and 3l have showed excellent antibacterial activity against all the tested bacterial strains as compared to the standard drug Ceftriaxone. Few of the compounds were found to be biologically potent. Molecular structure of compound 3i was confirmed by single crystal X-ray analysis. Springer Science+Business Media, LLC 2011.Item Synthesis and nonlinear optical characterization of new 1,3,4-oxadiazoles(2011) Chandrakantha, B.; Isloor, A.M.; Philip, R.; Mohesh, M.; Shetty, P.; Vijesh, A.M.A new series of 1,3,4-oxadiazole derivatives containing 2-fluoro-4-methoxy phenyl were synthesized by refluxing mixture of acid hydrazide 3 with different aromatic carboxylic acids (a-e) in phosphorous oxychloride. These newly synthesized compounds were characterized by NMR, mass spectral, and IR spectral studies, and also by C, H, N analyses. The open-aperture z-scan experiment was employed to measure the optical nonlinearity of the samples at 532 nm, using 5 ns laser pulses. The measurements indicate that compound 4a, which contains Bromine, behaves as an optical limiter at this wavelength, with potential applications in optoelectronics. Indian Academy of Sciences.Item Synthesis and biological evaluation of aminoketones(2010) Sankappa, Rai, U.; Isloor, A.M.; Shetty, P.; Isloor, N.; Malladi, S.; Fun, H.-K.A three-component Mannich reaction of different ketones with aromatic aldehydes and different amines in microwave irradiation under solvent free condition afforded corresponding ?-amino carbonyl compounds in excellent yields. This method proved as a novel and improved modification of the reported three-component Mannich reaction in terms of milder reaction conditions, reaction times, clean reaction profiles, very small quantity of catalyst and simple workup procedure. Newly synthesized ?-aminoketones were characterized by spectral studies. Structure of compound 4a was also confirmed by single-crystal X-ray analysis. All the compounds were screened for their antimicrobial activity by MIC method. Few of the molecules were found to be biologically potent. 2010 Elsevier Masson SAS. All rights reserved.Item Synthesis and anti-inflammatory evaluation of some new 3,6-disubstituted-1, 2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles bearing pyrazole moiety(2012) Malladi, S.; Isloor, A.M.; Shetty, P.; Fun, H.K.; Telkar, S.; Mahmood, R.; Isloor, N.In the present study, a new series of 3,6-disubstituted- 1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazoles (4aj) have been synthesized by condensing 3-substituted-4-amino-5- mercapto-1,2,4-triazoles (1a-b) with various 3-substitutedpyrazole- 4-carboxylic acids (3a-e) in the presence ofPOCl3. The structures of newly synthesized compounds were characterized by elemental analysis, IR, 1H NMR, 13CNMR, and mass spectroscopic studies. Structure of the compound 4b was also confirmed by recording the single crystal X-ray structure. All the synthesized compounds were screened for their anti-inflammatory activities by carrageenan induced paw edema method. Anti-inflammatory screening indicated that, compounds 4d, 4e, and 4h were found to be biologically active whereas remaining compounds showed poor antiinflammatory activity. Also molecular docking studies were also performed for compounds which showed good antiinflammatory activity. Springer Science+Business Media, LLC 2011.