Erbay Kalay , Oguz Özbek , Muhammed Elik , Caglar Berkel , Osman Nuri Aslan
{"title":"The synthesis, sensor and biological properties of two novel rhodanine derivative molecules","authors":"Erbay Kalay , Oguz Özbek , Muhammed Elik , Caglar Berkel , Osman Nuri Aslan","doi":"10.1016/j.jics.2025.101591","DOIUrl":"10.1016/j.jics.2025.101591","url":null,"abstract":"<div><div>Herein, two different rhodanine derivative molecules (<em>E</em>)-2-(5-(4-(((2,5-dichlorophenyl)sulfonyl)oxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)acetic acid <strong>(3)</strong> and (<em>E</em>)-2-(5-(4-(((4-bromophenyl)sulfonyl)oxy)benzylidene)-4-oxo-2-thioxothiazolidin-3-yl)acetic acid <strong>(4)</strong> have been synthesized for the first time. The characterization of these molecules was carried out using various spectroscopic techniques such as <sup>1</sup>H–, <sup>13</sup>C– NMR, FT–IR and Q–TOF. Sensor properties of the newly synthesized rhodanine derivative molecules were investigated in detail using potentiometric methods. For this purpose, different polymer membrane sensors in which these two molecules were used as ionophores in the design were prepared. Potentiometric performance properties were compared among these prepared sensors, using mixtures in which the most ideal potentiometric behavior of both molecules was observed. Among the two sensors, Sensor IX exhibited much higher selectivity against Cu<sup>2+</sup> ions compared to Sensor II. The sensors had linear and Nernstian responses in the concentration range of 1.0 × 10<sup>−1</sup>–1.0 × 10<sup>−5</sup> mol L<sup>−1</sup>. The detection limits of the sensors prepared with ionophore <strong>3</strong> and <strong>4</strong> were found to be 9.77 × 10<sup>−6</sup> mol L<sup>−1</sup> and 9.36 × 10<sup>−6</sup> mol L<sup>−1</sup>, respectively, indicating that both sensors have comparable limit of detection values. While the sensor prepared with <strong>4</strong> had a very fast response time of 5 s, the sensor prepared with <strong>3</strong> exhibited a response time of approximately 10 s. The sensors prepared with both molecules worked in a wide pH range (4.0–10.0) without being affected by pH changes. Both sensors were subsequently applied to various real samples, and very high recoveries were obtained. Based on these data, it can be stated that the newly synthesized rhodanine derivatives can be used as ionophores. However, there are particular differences in terms of selectivity and other potentiometric performance criteria between the two synthesized molecules. Lastly, the anti-microbial effects of these new molecules on six different bacteria were studied, and it was determined that the synthesized molecules inhibit the growth of some bacterial species to a certain extent.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101591"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140687","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Kinetics & mechanism of oxidation of indigo carmine dye with potassium peroxydisulphate in micellar and sub –micellar medium","authors":"Kalyana Chakravarthy Mutnuru , Ram Kumar Gummaluri , Ramakrishna Karipeddi","doi":"10.1016/j.jics.2024.101554","DOIUrl":"10.1016/j.jics.2024.101554","url":null,"abstract":"<div><div>Oxidation of Indigo carmine with potassium peroxydisulphate is investigated in presence of micelles under pseudo first order conditions in acidic medium. The reactants form suspensions with CTAB micelles under the established experimental conditions. There is no appreciable change in the rate with varying [Triton-X-100]. The reaction has shown first order kinetics with varying [Indigo carmine], [S<sub>2</sub>O<sub>8</sub><sup>2−</sup>] and is independent of varying [H<sup>+</sup>] in presence of anionic SDS and neutral Triton-X-100 micelles. The ionic strength is maintained using sodium perchlorate, and there is no ionic strength effect on the rate of the reaction.The rate of the reaction is accelerated with varying [SDS], reaching a maximum under a sub-micellar concentration of 7.0 × 10<sup>−4</sup> moldm<sup>−3</sup>. At higher SDS concentrations, the reaction rate is inhibited. The rate [surfactant] profile is showing a maximum, so the reaction is a typical bimolecular catalyzed reaction. The binding constant is determined by applying Piszkiewicz and Berezin kinetic models.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101554"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140663","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
A Haseena Begum , S. Savitha , T.M Naren Vidaarth , K.S.G. Jagan , S. Surendhiran , A. Karthik , B. Kalpana
{"title":"Design and optimization of Ag decorated MgO nanosphere catalyst for efficient removal of textile industry pollutants and their biological applications","authors":"A Haseena Begum , S. Savitha , T.M Naren Vidaarth , K.S.G. Jagan , S. Surendhiran , A. Karthik , B. Kalpana","doi":"10.1016/j.jics.2025.101573","DOIUrl":"10.1016/j.jics.2025.101573","url":null,"abstract":"<div><div>This study presents the biogenic synthesis of phytochemical-enriched magnesium oxide nanoparticles (MgO NPs) using <em>Eucalyptus globulus</em> leaf extract and silver-doped nanocomposites (MgO–Ag NCs) at varying silver concentrations (0.1, 0.3, and 0.5 mM). Comprehensive physicochemical analyses were conducted to evaluate the influence of silver incorporation on the properties of MgO NPs. The doping of Ag in MgO increased crystalline size from 38 nm to 44 nm without introducing an Ag-specific structural phase, suggesting the successful incorporation of Ag into the MgO lattice. Optical studies revealed a notable reduction in the bandgap, decreasing from 4.7 eV for pure MgO to 3.61 eV at higher Ag concentrations suitable for photocatalytic activity. The photocatalytic analysis demonstrated exceptional dye degradation efficiencies, with MgO–Ag NCs achieving 100 % Malachite Green (MG) and 97.9 % degradation of Congo Red (CR) degradation. Scavenging activity analyses provided insights into the degradation pathways facilitated by the nanocomposites. Additionally, the antibacterial efficacy of MgO–Ag NCs showed significant improvement, with zones of inhibition increasing from 13 mm for pure MgO to 21 mm for Ag-doped MgO against <em>Staphylococcus aureus</em> and from 9 mm to 18 mm against <em>Escherichia coli.</em> These findings highlight that Ag doping profoundly enhances the physicochemical properties, photocatalytic performance, and antibacterial activity of MgO NPs, underscoring their potential for applications in environmental remediation and biomedical fields.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101573"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140666","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Microwave-assisted synthesis of primary aryl/heteroarylamines via one-pot reductive amination: A convenient and efficient synthetic route","authors":"Hasan Saral , Özgür Özdamar , Yunus Bekdemir","doi":"10.1016/j.jics.2024.101539","DOIUrl":"10.1016/j.jics.2024.101539","url":null,"abstract":"<div><div>Microwave-assisted copper-catalyzed amination process can be established for the conversion of aryl/heteroaryl bromides. The key features of this study include diverse aryl/heteroarylamine synthesis, the catalyst amount, shorter reaction time, high yields, a one-pot procedure, simple and commercially available starting materials, and moderate to good reaction yields. We have shown that using Cu(OAc)<sub>2</sub> as a catalyst combined with ethylenediamine as an additive in the ethanol as solvent, greatly improved the reaction time and yield of this system compared to the previously reported conditions. The current catalytic system contributes a valuable route for preparing aminoquinoline and aminoisoquinoline as key precursors to obtain fine chemicals.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101539"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140729","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Youness El Bakri , Kandasamy Saravanan , Shaaban K. Mohamed , Amr H. Moustafa , Hatem A. Abuelizz , Rashad Al-Salahi , Eman A. Ahmed
{"title":"Exploring non-covalent interactions in oxazolidine derivatives: Synthesis, X-ray diffraction, and quantum chemical studies","authors":"Youness El Bakri , Kandasamy Saravanan , Shaaban K. Mohamed , Amr H. Moustafa , Hatem A. Abuelizz , Rashad Al-Salahi , Eman A. Ahmed","doi":"10.1016/j.jics.2025.101596","DOIUrl":"10.1016/j.jics.2025.101596","url":null,"abstract":"<div><div>In this work, two oxazolidine derivatives <strong>4</strong> and <strong>5</strong> were conveniently prepared in high yields via the reaction of pseudoephedrine <strong>1</strong> with the corresponding bis(methythio)yledinenitriles <strong>2</strong> and/or <strong>3</strong>, respectively using both ultrasonic and microwave irradiation techniques. The yields of oxazolidines <strong>4</strong> and <strong>5</strong> were summarized and compared with their preparation by traditional methods. X-ray diffraction analysis uncovers that a multitude of non-covalent interactions collaborate to establish the arrangement of crystals and the behavior of supramolecular assemblies in the solid state. The quantification of all intermolecular interactions is achieved through Hirshfeld surface analysis and fingerprint plots, while energy frameworks are constructed to examine the predominant energy interactions that contribute to the strength of molecular packing. In the experimental investigation, we conducted a thorough theoretical analysis employing quantum chemical techniques to ascertain the characteristics of the derivatives. The comparison of geometrical parameters revealed a strong agreement with the experimental findings. QTAIM has been used to analyze and characterize both covalent and non-covalent bonds. The closed-shell interactions at the bond critical point confirm the presence of non-covalent interactions.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101596"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140791","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Effect of different electrode configuration modes on the performance of electrocoagulation","authors":"Vinod Kumar Jaiswar, Anil K. Saroha","doi":"10.1016/j.jics.2025.101569","DOIUrl":"10.1016/j.jics.2025.101569","url":null,"abstract":"<div><div>The effect of electrode configuration on the performance of electrocoagulation has been studied by performing experiments to treat synthetic dye solution (100 ppm) containing reactive orange 4 (RO4) dye using aluminum electrodes in bipolar (BP), monopolar series (MP-S), & monopolar parallel (MP-P) connection modes. The experimental results were interpreted in terms of color removal efficiency (CRE), electrical energy consumption (EEC) & operating cost (OC). The BP connection mode was found to be efficient as the rate of color removal, CRE, EEC & OC were found to be maximum for the BP connection mode, followed by MP-S and MP-P connection mode. The experiments were conducted at the applied current of 0.05 A, pH of 6.1 ± 0.1, inter-electrode distance of 1.0 cm, agitation speed of 200 rpm, and CRE was found to be 97.12 % for BP, 96.14 % for MP-S, and 94.02 % for MP-P connection mode. Since the rate of color removal and CRE was highest in the BP connection mode, the kinetic study for dye removal was performed for the BP connection mode and it was noticed that the removal of RO4 dye from its synthetic solution follows a second-order model.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101569"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140667","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Busra Kus , Mesut Sezer , Melike Isgoren , Sevil Veli
{"title":"Anodic electrooxidation of textile wastewater by using spray coating Ti/TiO2–RuO2–IrO2 anode: Response surface optimization of the process","authors":"Busra Kus , Mesut Sezer , Melike Isgoren , Sevil Veli","doi":"10.1016/j.jics.2025.101595","DOIUrl":"10.1016/j.jics.2025.101595","url":null,"abstract":"<div><div>This study investigated wastewater treatment by a local textile company using an electrooxidation (EO) process. A Ti/TiO<sub>2</sub>–RuO<sub>2</sub>–IrO<sub>2</sub> electrode produced by spray coating was used as the anode. The EO process variables used to treat textile wastewater were optimized using the Box-Behnken Design. Color, COD, and TOC removal were selected as the model responses. Under optimum conditions (pH 3, current density 58.03 mA cm<sup>−2</sup>, and 3.04 h), the optimization resulted in removal efficiencies of 97 % for color, 84 % for COD, and 53 % for TOC. The operating cost under optimal conditions was calculated to 6.01 $ (kg COD)<sup>−1</sup>. A novel spray coating technique was successfully employed to fabricate Ti/TiO<sub>2</sub>–RuO<sub>2</sub>–IrO<sub>2</sub> electrodes for wastewater treatment via the EO process. The optimized EO process using this anode offers a promising, low-cost, and rapid method for large-scale wastewater treatment.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101595"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140675","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
B. Mahalakshmi , S. Sivakumar , Nazir Ahmad Mala , E. Manikandan
{"title":"Exploring the potential of Ni-doped CuO nanoparticles as a promising electrode material for asymmetric supercapacitors","authors":"B. Mahalakshmi , S. Sivakumar , Nazir Ahmad Mala , E. Manikandan","doi":"10.1016/j.jics.2025.101589","DOIUrl":"10.1016/j.jics.2025.101589","url":null,"abstract":"<div><div>In the current study, monoclinic Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.00, 0.03, 0.05, 0.07 M) nanoparticles (NPs) were prepared using the chemical precipitation method. NPs resulting from this process are named NC0 (pure), NC3 (3 %), NC5 (5 %), and NC7 (7 %). The X-ray diffraction confirmed the Ni ions were successfully substituted into the CuO lattice and the crystallite size of the nanoparticles showed a decreasing trend. Scanning electron microscopy confirmed the surface morphology of samples NC0 and NC7 are rod-like and flower-like. The cyclic voltammetry (CV) and galvanostatic charge-discharge tests in 2 M KOH, the pseudocapacitive behaviour of the Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.00, 0.07 M) electrodes was examined. The computed values of specific capacitance (Cs) for the Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.00) electrode are 433.33 F/g, while the corresponding value for the Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.07) electrode is 578.97 F/g at scan rates of 5 mV/s. GCD curves demonstrate that Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.00, 0.07 M) electrodes have specific capacitance (Cp) of 238.98, and 396.67 F/g at a current density of 1 A/g. After 2000 cycles, the retention was 88.36 % and the increased coulombic efficiency was 85.74 % at Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.07 M) electrode. Vibrating sample magnetometer are characteristics at room temperature and found that Cu<sub>1-x</sub>Ni<sub>x</sub>O (x = 0.00, 0.03, 0.05, 0.07 M) becomes ferromagnetic behaviour.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101589"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140682","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Vanillin synthesis: Harnessing lignin resources from pulpwood trees through oxidative cleavage depolymerization","authors":"Prasanth Vasu , Kandeeban Rajagopalan , Gayathri Chellasamy , Mirko Magni , Kyusik Yun , Manivannan Subramanian , Yuvaraj Haldorai , M.S. Sivaramkumar","doi":"10.1016/j.jics.2024.101555","DOIUrl":"10.1016/j.jics.2024.101555","url":null,"abstract":"<div><div>This study aims to assess the potential yield of vanillin from pulp-industry black liquor using alkaline hydrolysis with oxidative cleavage depolymerization techniques in different pulpwood tree species: Casuarina, Leucaena, Eucalyptus, and Eucalyptus hybrid clone. The highest vanillin content was found in the black liquor from Eucalyptus (3.03 %), followed by Eucalyptus hybrid clone (2.11 %), Leucaena (0.55 %), and Casuarina (0.25 %). Further studies are required to identify the Eucalyptus varieties offering higher vanillin yields for potential commercial implementation.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101555"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140717","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"Polyurethane matrix as an oxide@biochar composite supports employed in heterogeneous photocatalysis","authors":"Laryssa Cristine Ribeiro dos Santos , Larissa Bach-Toledo , Glauco Meireles Mascarenhas Morandi Lustosa , Bruna Andressa Bregadiolli , Waldir Antônio Bizzo , Talita Mazon","doi":"10.1016/j.jics.2024.101559","DOIUrl":"10.1016/j.jics.2024.101559","url":null,"abstract":"<div><div>The contamination of liquid effluents with toxic and persistent substances has significant socioeconomic and environmental impacts, and the Advanced Oxidative Processes (AOPs) have shown great promise in eliminating and disinfecting wastewater. In this context, we developed a low-cost photolytic system to improve the efficiency of methylene blue (MB) dye removal. Based on biochar derived from sugarcane biomass, the proposed composites were prepared with various metal oxides (TiO<sub>2</sub>, ZnO, and CuO). Their photocatalytic property was tested in the dispersion of the biochar composite powder in the solution and a biochar composite-based porous matrix built from a commercial polyurethane sponge. High photodegradation rates of the MB dye were observed: 96 % and 98 % for dispersed powder of TiO<sub>2</sub>@biochar and ZnO@biochar, respectively, in 230 min and at room temperature. By applying a temperature of 50 °C, an efficiency of 95 % was achieved within 30 min of the photocatalysis. When immobilized on the polyurethane (PM) matrix, the results for TiO<sub>2</sub>@biochar and ZnO@biochar showed the same tendency. After three heterogeneous photocatalysis cycles, both materials showed promising results for reuse. Moreover, the main advantage of using the PM matrix is the easy recovery, avoiding significant material loss. These findings reveal a significant interaction between metal oxides and biochar from the sugarcane industry, suggesting its potential use as a semiconductor in heterogeneous photocatalysis.</div></div>","PeriodicalId":17276,"journal":{"name":"Journal of the Indian Chemical Society","volume":"102 2","pages":"Article 101559"},"PeriodicalIF":3.2,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143140726","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}