Faculty Publications
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Item A rapid extractive spectrophotometric determination of copper(II) in environmental samples, alloys, complexes and pharmaceutical samples using 4-N,N(dimethyl)amino]benzaldehyde thiosemicarbazone(2011) Karthikeyan, J.; Naik, P.P.; Nityananda Shetty, A.N.4-[N,N-(Dimethyl)amino]benzaldehyde thiosemicarbazone (DMABT) is proposed as an analytical reagent for the extractive spectrophotometric determination of copper(II). DMABT forms yellow colored complex with copper(II) in the pH range 4.4-5.4. Beer's law is obeyed in the concentration range up to 4.7 ?g mL -1. The optimum concentration range for minimum photometric error as determined by Ringbom plot method is 1.2-3.8 ?g mL-1. The yellowish Cu(II)-DMABT complex shows a maximum absorbance at 420 nm, with molar absorptivity of 1.72 × 104dm3 mol-1 cm-1 and Sandell's sensitivity of the complex obtained from Beer's data is 0.0036 ?g cm-2. The composition of the Cu(II)-DMABT complex is found to be 1:2 (M/L). The interference of various cations and anions in the method were studied. Thus the method can be employed for the determination of trace amount of copper(II) in water, alloys and other natural samples of significant importance. © 2010 Springer Science+Business Media B.V.Item Dual colorimetric receptor with logic gate operations: Anion induced solvatochromism(Royal Society of Chemistry, 2014) Kigga, M.; Swathi, N.; Manjunatha, J.R.; Das, U.K.; Nityananda Shetty, A.N.; Trivedi, D.R.A receptor R1 was designed and synthesised for colorimetric detection of F- ions as well as Cu2+ ions via intramolecular charge transfer mechanism. Upon addition of F- ions in dry DMSO, the color of the receptor R1 changed from pale yellow to blue. The receptor showed a unique property of solvatochromism by displaying different coloration with different solvents only in the presence of F- ions, which were applied to determine the percentage composition of binary solvent mixtures. The receptor R1 was able to detect Cu2+ ions colorimetrically where it exhibited a color change from pale yellow to orange-red. In addition, the receptor was subjected to molecular logic gate applications, wherein it showed 'ON-OFF' switching operations. © 2014 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.Item Colorimetric and fluorometric turn-on sensor for selective detection of fluoride ions: Sol-gel transition studies and theoretical insights(Royal Society of Chemistry, 2018) Pangannaya, S.; Mohan, M.; Trivedi, D.R.A new organic receptor R1 based on a naphthyl unit covalently linked to a long alkyl chain has been designed, synthesized and characterized by standard spectroscopic techniques. The colorimetric response of receptor R1 from colorless to a pale yellow color and blue fluorescence emission in the presence of F- ions revealed its selective sensing ability in the solution phase. UV-Vis titration, fluorescence titration and 1H NMR titration studies confirmed the formation of the R1-F- complex. Receptor R1 formed a stable gel in DMSO and was confirmed through the standard heating-and-cooling method. Addition of F- ions resulted in disruption of the gel forming a solution that exhibited blue fluorescence emission. The binding constant of the R1-F- complex was found to be of the order of 5.9 × 105 M-1. DFT studies revealed the formation of the receptor-anion complex agreeing well with the experimental results. The detection limit was calculated and found to be 0.8 ppm, implying the potential for application of receptor R1 in environmental applications. © 2018 The Royal Society of Chemistry and the Centre National de la Recherche Scientifique.Item Colorimetric anion sensors based on positional effect of nitro group for recognition of biologically relevant anions in organic and aqueous medium, insight real-life application and DFT studies(Elsevier B.V., 2018) Singh, A.; Sahoo, S.K.; Trivedi, D.R.A new six colorimetric receptors A1-A6 were designed and synthesized, characterized by typical common spectroscopic techniques like FT-IR, UV–Visible, 1H NMR, 13C NMR and ESI-MS. The receptor A1 and A2 exhibit a significant naked-eye response towards F? and AcO? ions in DMSO. Due to presences of the NO2 group at para and ortho position with extended ?-conjugation of naphthyl group carrying –OH as a binding site. Compared to receptor A2, A1 is extremely capable of detecting F? and AcO? ions present in the form of sodium salts in an aqueous medium. This is owed to the occurrence of –NO2 group at para position induced in increasing the acidity of –OH proton. Consequently, it easily gets deprotonated in aqueous media. The detection limit of receptor A1 was turned out to be 0.40 and 0.35 ppm for F? and AcO? ions which is beneath WHO permission level (1.0 ppm). Receptor A1 shows a solitary property of solvatochromism in different aprotic solvents in presence of AcO? ion. Receptor A1 depicts high selectivity towards AcO? ion in DMSO: HEPES buffer (9:1, v/v). Receptor A1 proved itself for real life application by detecting anion in solution and solid state. The binding mechanism of receptor A1 with AcO? and F? ions was monitored from 1HNMR titration and DFT study. © 2017 Elsevier B.V.Item Inhibition of Na + /K + - and Ca 2+ -ATPase activities by phosphotetradecavanadate(Elsevier Inc. usjcs@elsevier.com, 2019) Fraqueza, G.; Fuentes, J.; Krivosudský, L.; Dutta, S.; Mal, S.S.; Roller, A.; Giester, G.; Rompel, A.; Aureliano, M.Polyoxometalates (POMs)are promising inorganic inhibitors for P-type ATPases. The experimental models used to study the effects of POMs on these ATPases are usually in vitro models using vesicles from several membrane sources. Very recently, some polyoxotungstates, such as the Dawson anion [P 2 W 18 O 62 ] 6? , were shown to be potent P-type ATPase inhibitors; being active in vitro as well as in ex-vivo. In the present study we broaden the spectrum of highly active inhibitors of Na + /K + -ATPase from basal membrane of epithelial skin to the bi-capped Keggin-type anion phosphotetradecavanadate Cs 5.6 H 3.4 PV 14 O 42 (PV 14 )and we confront the data with activity of other commonly encountered polyoxovanadates, decavanadate (V 10 )and monovanadate (V 1 ). The X-ray crystal structure of PV 14 was solved and contains two trans-bicapped ?-Keggin anions H x PV 14 O 42 (9-x)- . The anion is built up from the classical Keggin structure [(PO 4 )@(V 12 O 36 )]capped by two [VO]units. PV 14 (10 ?M)exhibited higher ex-vivo inhibitory effect on Na + /K + -ATPase (78%)than was observed at the same concentrations of V 10 (66%)or V 1 (33%). Moreover, PV 14 is also a potent in vitro inhibitor of the Ca 2+ -ATPase activity (IC 50 5 ?M)exhibiting stronger inhibition than the previously reported activities for V 10 (15 ?M)and V 1 (80 ?M). Putting it all together, when compared both P-typye ATPases it is suggested that PV 14 exibited a high potential to act as an in vivo inhibitor of the Na + /K + -ATPase associated with chloride secretion. © 2019 The AuthorsItem Design and synthesis new colorimetric receptors for naked-eye detection of biologically important fluoride and acetate anions in organic and arsenite in aqueous medium based on ICT mechanism: DFT study and test strip application(Elsevier B.V., 2020) Singh, A.; Mohan, M.; Trivedi, D.R.Novel three colorimetric anion receptors R1, R2 and R3 have been designed and synthesized via condensation reaction and characterized using IR, MS, and NMR spectroscopic techniques. Anion sensing properties were studied using colorimetric, UV–vis titration, 1H NMR titration, and Cyclic Voltammetric Studies. Comparing the UV–visible titration data of the receptors R1 and R2, R2 showed high redshift (??max) in the mixed competitive solution (DMSO: H2O, 9: 1; v/v) of about 155 nm, 157 nm, 169 nm for Na+F?, Na+AcO?, and Na+AsO2 ? ions with LOD of 0.23 ppm, 0.18 ppm, and 0.30 ppm, respectively. The observed spectral change of receptor R2 is due to the anion-induced deprotonation of the OH proton, which is confirmed by UV–vis titration, 1HNMR titration, and cyclic voltammetric studies. Theoretical studies via DFT calculation were carried for R1 and R2 to optimize the structure and to explain the anion-binding mechanism. The application of designed receptor R2 was successfully demonstrated for the detection of F? and AsO2 ? ions using a test strip. The receptors R1 and R2 proved itself to be potentially useful for real-life application by sensing F? and AcO? ions in real samples like toothpaste, mouthwash, vinegar and seawater in a complete aqueous medium. © 2019 Elsevier B.V.Item Design and synthesis of malonohydrazide based colorimetric receptors for discrimination of maleate over fumarate and detection of F?, AcO? and AsO2 ? ions(Elsevier B.V., 2020) Singh, A.; Mohan, M.; Trivedi, D.R.In this study, we have designed and synthesized two new organic receptors R1 and R2 based on malonohydrazide for the recognition of biologically important anions. The receptor R1 capable of colorimetric discrimination of maleate over fumarate ion, exhibit significant color change from pale yellow to wine red due to intermolecular hydrogen bond between the R1 and maleate ion, supported by 1HNMR titration, where the peak at ?12.0 ppm attributed to the NH proton experiences a downfield shift upon binding with maleate ion. Receptor R1, equipped with two electron-withdrawing [sbnd]NO2 moieties as the chromogenic signaling unit enhance the hydrogen bonding tendency and acidity, and thus when comparing with receptor R2, R1 displayed substantial higher redshift (??max) of 148 nm, 143 nm, and 140 nm towards F?, AcO?, and maleate anion in the DMSO. In addition, the synthesized receptors R1 and R2 are able to detect F?, AcO?, and AsO2 ? ions as their sodium salts in an aqueous solution with visual color change. Receptor R1 exhibit electrochemical response towards F? and AcO? ions. The receptors R1 and R2 are successfully applied for quantitative detection of F? ion in the toothpaste solution in an aqueous medium. Additionally, R1 and R2 exhibit fluorescence enhancement towards F? and AcO? ions in the DMSO. As well, R1 and R2 demonstrate to be potentially useful colorimetric chemosensor for sensing maleate ion using the test strip. The theoretical calculation based on TD-DFT corroborates well with the experimental results of the receptors R1 and R2 with fluoride, acetate and maleate. © 2019 Elsevier B.V.Item Colorimetric differentiation of arsenite and arsenate anions using a bithiophene sensor with two binding sites: DFT studies and application in food and water samples(Royal Society of Chemistry, 2024) K, K.; Nityananda Shetty, A.N.; Trivedi, D.R.Chemosensor N7R1 with two acidic binding sites was synthesized, and the ability of the sensor to differentiate arsenite and arsenate in the organo-aqueous medium was evaluated using colorimetric sensing methods. N7R1 distinguished arsenite with a peacock blue color and arsenate with a pale green color in a DMSO/H2O (9 : 1, v/v) solvent mixture. The specific selectivity for arsenite was achieved in DMSO/H2O (7 : 3, v/v). The sensor demonstrated stability over a pH range of 5 to 12. The computed high binding constant of 9.3176 × 1011 M−2 and a lower detection limit of 11.48 ppb for arsenite exposed the chemosensor's higher potential for arsenite detection. The binding mechanism with a 1 : 2 binding process is confirmed using UV-Vis and 1H NMR titrations, electrochemical studies, mass spectral analysis and DFT calculations. Practical applications were demonstrated by utilizing test strips and molecular logic gates. Chemosensor N7R1 successfully detected arsenite in real water samples, as well as honey and milk samples. © 2024 The Royal Society of Chemistry.Item Selective Chromogenic Chemosensors for Arsenite Anion: A Facile Approach to Analyzing Arsenite in Honey, Milk, and Water Samples(John Wiley and Sons Inc, 2024) K, K.; Nityananda Shetty, A.N.; Trivedi, D.R.In this study, two chemosensors, N5R1 and N5R2, based on 5-(4-nitrophenyl)-2-furaldehyde, with varying electron-withdrawing groups, were synthesized and effectively employed for the colorimetric selective detection of arsenite anions in a DMSO/H2O solvent mixture (8 : 2, v/v). Chemosensors N5R1 and N5R2 exhibited a distinct color change upon binding with arsenite, accompanied by a spectral shift toward the near-infrared region (??max exceeding 200 nm). These chemosensors established stability between a pH range 6–12. Among them, N5R2 displayed the lowest detection limit of 17.63 ppb with a high binding constant of 2.6163×105 M?1 for arsenite. The binding mechanism involved initial hydrogen bonding between the NH binding site and the arsenite anion, followed by deprotonation and an intramolecular charge transfer (ICT) mechanism. The mechanism was confirmed through UV and 1H NMR titrations, cyclic voltammetric studies, and theoretical calculations. The interactions between the sensor and arsenite anions were further analyzed using global reactivity parameters (GRPs). Practical applications were demonstrated through the utilization of test strips and molecular logic gates. Real water samples, honey, and milk samples were successfully analyzed by both chemosensors for the sensing of arsenite. © 2024 Wiley-VCH GmbH.Item Chromogenic Chemosensor for Simultaneous Detection of PO43? and CO32? Anions in Organo-Aqueous Solutions: Application in Arduino Based Electronic Color Sensor Device and Logic Gate(John Wiley and Sons Inc, 2024) Dhawale, A.; Trivedi, D.R.Three new chromogenic receptors have been synthesized with the primary objective of facilitating the selective recognition of PO43?and CO32? ions in an organo-aqueous medium. R1 and R2 exhibit an extraordinary detection limit aligning with both EPA and WHO guidelines. R1 shows LOD of 0.135 ppm for PO43? and 0.175 ppm for CO32?, while R2 sets forth a LOD of 0.427 ppm for PO43? and 0.729 ppm for CO32?. The binding mechanism involves intramolecular charge transfer (ICT) band are substantiated by comprehensive studies that include UV-Vis titration, 1H-NMR titration, DFT studies and electrochemical studies. Chemosensors were employed in the formulation of logic gate, the fabrication of a paper strip test kit and its application in RGB color sensor device. © 2024 Wiley-VCH GmbH.