Faculty Publications
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Item Insights into the electrooptical anion sensing properties of a new organic receptor: Solvent dependent chromogenic response and DFT studies(Royal Society of Chemistry, 2016) Pangannaya, P.; Tarafder, K.; Nityananda Shetty, A.N.; Trivedi, D.R.A highly selective hydrazine based electrooptical receptor featuring solvent based color transition properties in the presence of acetate ions has been developed. The AcO- ion mediated color transition properties of a new organic receptor in solvents of varying polarity highlights the influence of dipole moment in stabilizing the excited state. Selective detection of acetate ions by a new organic receptor in the presence of DMSO : Tris HCl buffer (9 : 1, v/v) has been the pivotal concept of the present work. 1H-NMR titration and DFT studies provide quantitative proof of the underlying detection mechanism. Solution and solid state sensing response of anions by the receptor reflects the practical utility in real time sample analysis. © 2016 The Royal Society of Chemistry.Item Electrooptical characteristics and anion binding behaviour of organic receptors: Effect of substitution on colorimetric response(Elsevier B.V., 2017) Pangannaya, S.; Trivedi, D.R.A series of four organic receptors, R1, R2, R3 and R4 possessing [sbnd]NH unit as binding site with varied positional substitution of [sbnd]OH and [sbnd]NO2functionalities have been synthesized and studied for their anion binding ability. Significant changes were observed in the UV–vis spectra of receptors with the addition of AcO?ion justifying the observed color changes visible to naked eye. Receptors R1, R2 and R3 showed mild color changes in the presence of F?and H2PO4 ?ions whereas R4 exhibited selective response towards AcO?ion. UV–vis titration and cyclic voltammetric studies performed with the incremental addition of AcO?ion to the receptors confirmed the anion binding process. The band gap value derived from the experimental results of UV–vis spectroscopic and cyclic voltammetric studies support the formation of AcO?ion-receptor complex. 1H NMR titration studies performed with the addition of AcO?ion to receptor R3 confirms the deprotonation of the [sbnd]NH proton involved in the binding mechanism. © 2017 Elsevier B.V.Item Design and synthesis of a new organic receptor and evaluation of colorimetric anion sensing ability in organo-aqueous medium(Elsevier B.V., 2017) Pangannaya, S.; Tarafder, K.; Trivedi, D.R.A new organic receptor has been designed and synthesized by the combination of aromatic dialdehyde with nitro-substituted aminophenol resulting in a Schiff base compound. The receptor exhibited a colorimetric response for F? and AcO? ion with a distinct color change from pale yellow to red and pink respectively in dry DMSO solvent and yellow to pale greenish yellow in DMSO:H2O (9:1, v/v). UV–Vis titration studies displayed a significant shift in absorption maxima in comparison with the free receptor. The shift could be attributed to the hydrogen bonding interactions between the active anions and the hydroxyl functionality aided by the electron withdrawing nitro substituent on the receptor. 1H NMR titration and density functionality studies have been performed to understand the nature of interaction of receptor and anions. The lower detection limit of 1.12 ppm was obtained in organic media for F? ion confirming the real time application of the receptor. © 2016Item 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 Hydrazinylpyridine based highly selective optical sensor for aqueous source of carbonate ions: Electrochemical and DFT studies(Elsevier B.V., 2018) Thimaradka, V.; Pangannaya, S.; Mohan, M.; Trivedi, D.R.A series of new receptors PDZ1–3 based on 2-(arylidenehydrazinyl)pyridines have been designed and synthesized for the detection of biologically and environmentally important ions. The colorimetric detection of CO32 ? using neutral organic receptor PDZ-1 has been achieved with characteristic visual colour change from yellow to green accompanied by a large redshift of 215 nm in absorption maxima. UV–Vis spectroscopic and cyclic voltammetric studies reveal the stoichiometry of binding and electrochemistry of host-guest complex formation. The binding constant was found to be 0.77 × 104 M? 2. In addition, electrochemical studies provide an insight into the stability of the complex. DFT studies performed on the PDZ-1 and PDZ-1 ? CO32 ? complex reveal the binding mechanism involved in the anion detection process. PDZ-1 is highly selective for carbonate and does not show any colorimetric response towards any other anions or cations, while PDZ-2 and PDZ-3 remain inactive in the ion detection process. The limit of detection (LOD) and limit of quantification (LOQ) of PDZ-1 for carbonate was found to be 0.11 mM and 0.36 mM respectively. Considerable binding constant and limit of detection make PDZ-1 to be used as a real time sensor for the detection of carbonate in environmental and biological samples. © 2017 Elsevier B.V.Item Substituent effect on colorimetric detection of biologically and environmentally relevant anions: Insight in real-life applications(Elsevier B.V., 2019) Singh, A.; Girish Gowda, R.; Trivedi, D.A new set of chromogenic anion receptors R1-R4 have been synthesized with a different substituent, including electron withdrawing (nitro moiety in R1), conjugated group (naphthyl in R2), and electron donating (methyl in R3), respectively. The receptors R1-R4 exhibited very good sensitivity towards the F ? and AcO ? anions in the DMSO. In addition, R1 showed selectivity towards H 2 PO 4 ? ions over other tested anions. R1 especially acted as an effective sensor for sodium salts of F ? , AcO ? , AsO 2 ? , and AsO 4 2? ions in an aqueous medium due to the presence of two electron-withdrawing nitro substituents, which showed hydrogen bond donor tendency and acidity of the OH proton. This result indicates that R1 is highly capable of competing with an aqueous medium to detect anions without counter Na + ion interference. Interestingly, R1 displays solvatochromic property in the presence of AcO ? ions in different aprotic solvents. Additionally, the receptor R1 shows high binding affinity towards AcO ? ions in the buffer medium (DMSO: HEPES, 9:1 v/v), which displayed remarkable colour change from pale yellow to blue with a large ?? red shift of 170 nm. The CV studies reveal the deprotonation of the -NH proton upon interaction with the AcO ? ions. The receptor R1 is subjected to practical application to sense F ? and AsO 2 ? ions using the test strip. In addition, the receptor R1 proves itself as a potential applicant for the detection of F ? ions quantitatively in commercially available mouthwash. © 2019 Elsevier B.V.Item Investigating the solubility of petroleum asphaltene in ionic liquids and their interaction using COSMO-RS(Korean Society of Industrial Engineering Chemistry A-803 Twin Bldg 275-3 Yangjae-Dong Seocho-Kul Seoul 137-130, 2019) Rashid, Z.; Wilfred, C.D.; Iyyaswami, I.; Arunagiri, A.; Murugesan, M.Dispersion of asphaltene in crude oil using ionic liquids (ILs) is being considered as a viable solution, in extraction and transportation processes. In this work, the interplay between asphaltene and ILs has been studied systematically to understand the effect of structural variation of ILs on asphaltene solubility. The activity coefficient of the total of 1517 ILs with different combinations of cation and anion of ILs for representative asphaltene molecule (asphaltene) was estimated via COSMO-RS (Conductor-like Screening Model for Real Solvents). COSMO_RS predictions were validated using experimental data on asphaltene solubility. Among the studied ILs, asphaltene showed high solubility in imidazolium-based ILs with hydrophobic anions. The present approach paved a way forward to rationally understand the impact of structural variation of ILs on their interaction with asphaltene molecule and to design new ILs for the dispersion and stabilization of asphaltene. © 2019 The Korean Society of Industrial and Engineering ChemistryItem 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 recognition of water-polluting inorganic arsenic anions using near-infrared chemosensors in organic and semi-aqueous medium(Springer Science and Business Media Deutschland GmbH, 2023) K, K.; Nityananda Shetty, A.N.; Trivedi, D.R.Highly sensitive and selective chemosensors N2R1–N2R3 for detecting water-polluting inorganic arsenic anions, arsenite, and arsenate were synthesized and characterized. The selectivity of anions was studied in the pure organic media as well as the organo-aqueous media. Receptors N2R1 and N2R3 exhibited selectivity toward arsenite ion over arsenate ion in the acetonitrile media with a Limit of Detection (LOD) of 0.119 ppm and 0.323 ppm, respectively. In 30% aq. DMSO, receptors N2R1–N2R3 displayed selectivity toward arsenite and arsenate with a better LOD of 0.044 ppm. The anion binding to the receptor achieved a spectral absorption shift toward the near-infrared region in both organic and aqueous media, making the receptors better colorimetric sensors. The cyclic voltammetric investigations, 1H–NMR titration, UV–Vis titration, and DFT experiments provided strong evidence for the initial H-bonding upon interaction with the anions and the subsequent deprotonation pathway for the detection of inorganic arsenic anions. © 2023, King Abdulaziz City for Science and Technology.