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Abstract Over the past decades, tremendous effort has been made to enhance the water‐splitting via fabricating eco‐friendly electrocatalyst with increased conductivity, and large number of accessible active sites in lab scale. However, the development of earth abundant efficient electrocatalyst with superior activity for ‐seawater‐splitting remains a great challenge for the researchers. In this regard, self‐supported catalysts are found to be the most promising candidates, they have the features of increased loading, superior adhesion, rapid mass and charge transfer, and easy wettability for large scale hydrogen production via electrochemical seawater splitting. This review investigates different fabrication processes for the self‐supported catalyst, emphasizing their distinct characteristics that contribute to improved activity. Furthermore, we provided a detailed elucidation of the procedure and characteristics of seawater splitting, emphasizing the most recent progress in the creation of self‐supportive catalyst for the hydrogen evolution reaction (HER), oxygen evolution reaction (OER), and bifunctional activity. We have also examined the current barriers and potential prospects for advancing the utilization of self‐supported catalysts in the process of seawater splitting.

Nitrogen cycling in pasture soils differing in drainage characteristics and fertilization legacy needs more research to determine efficient nutrient management strategies. This study compared differences in nitrate (NO3−), ammonium (NH4+), inorganic N (IN = NO3− + NH4+), potentially mineralizable nitrogen (PMN), loss-on-ignition carbon (C), and soil pH in 10, 0.7 ha pastures in Eatonton, Georgia, historically fertilized with the same amount of N as either broiler litter (BL; >15 years, 6 pastures) or mineral fertilizer (Min; 4 pastures). We sampled to 90 cm (0–5, 5–10, 10–20, 20–40, 40–60, and 60–90 cm) on a 20 m grid. An analysis of variance indicated that below 5 cm BL pastures had significantly greater amounts of NO3−, IN, PMN, and soil pH compared to Min pastures. Comparisons of drainage classes (well drained~WD, moderately well drained~MWD, and somewhat-poorly drained~SPD) for each BL and Min were analyzed using linear regression for C:IN, C:PMN, pH: NO3−, and pH: NH4+ with all depths combined. In MWD soils, BL had 0.1 and 0.2 mg N kg−1 greater PMN and IN, respectively, for each unit increase in C. In WD soils NO3− decreased in BL by 7.4 and in Min by 12.1 mg N kg−1, while in MWD soils, this level decreased in BL by 7.8 and in Min by 4.5 mg N kg−1 for each pH unit. Five years after N fertilization stopped, BL soils have retained more inorganic N but are losing more NO3− at a greater rate in the MWD soils when all depths are considered. These losses are a combination of plant uptake, emissions, runoff and leaching. While more research is needed, these results strongly suggest the need to design N fertilization practices with drainage class and fertilization legacy in mind to improve N-use efficiency.

The need for novel approaches to the treatment of colon cancer, a common and deadly disease, is universal. In this compilation, we look at how polymeric nanoparticles (Polymeric nanoparticles) could be used to treat colon cancer. Advantages of Polymeric nanoparticles in Fig.hting this disease include targeted medication administration, enhanced therapy efficacy, and fewer adverse effects. Their impact on cancer treatment is huge. Drug release and miRNA play crucial roles in this struggle by enabling early disease identification, individualised treatment strategies, and bolstering PONP mechanisms. The most up-to-date developments in the use of biomarkers in the diagnosis and prognosis of colon cancer are also discussed. Biomarkers used in toxicology range from genes to epigenomes to molecules. Better patient outcomes can be expected when biomarkers are used in conjunction with Polymeric nanoparticles for personalised treatment and cytotoxicity assessment. This strategy has the potential to completely transform cancer care by putting the needs of each patient first. Combining therapeutic and diagnostic capabilities inside a single nanoparticle system, the use of drug delivery and miRNA elevates the concept of theranostic applications employing Polymeric nanoparticles in colon cancer. This novel method enables toxicological and diagnostic capabilities to visualise and monitor colon cancer treatment with tailored drug administration. Additional research and clinical validation are necessary to implement these developments in clinical practise. There is reason to be optimistic about the future of cancer therapy when Polymeric nanoparticles are used in conjunction with standard medical care.

A robust method was developed using LC-ESI-MS/MS-based identification and quantification of 103 fortified pesticides in a mango fruit drink. Variations in QuEChERS extraction (without buffer, citrate, and/or acetate buffered) coupled with dispersive clean-up combinations were evaluated. Results showed 5 mL dilution and citrate buffered QuEChERS extraction with anhydrous (anhy) MgSO4 clean-up gave acceptable recovery for 100 pesticides @ 1 μg mL−1 fortification. The method was validated as per SANTE guidelines (SANTE/11813/2021). 95, 91, and 77 pesticides were satisfactorily recovered at 0.1, 0.05, and 0.01 μg mL−1 fortification with HorRat values ranging from 0.2–0.8 for the majority. The method showed matrix enhancement for 77 pesticides with a global uncertainty of 4.72%–23.89%. The reliability of the method was confirmed by real sample analysis of different brands of mango drinks available in the market. The greenness assessment by GAPI (Green Analytical Procedure Index) indicated the method was much greener than other contemporary methods.

Coumarins, in general, exhibit a wide range of photophysical characteristics and are highly sensitive to their microenvironment, and, therefore, their fluorescence characteristics have attracted immense attention as sensors in chemical and biological systems. In the present study, the supramolecular interaction of a bichromophoric coumarin dye, namely, Coumarin 7 (C7) with sulfobutylether-β-cyclodextrin (SBE7βCD) macrocyclic host at different pH conditions has been investigated by using optical spectroscopic techniques such as absorption, steady-state and time-resolved emissions, and circular dichroism measurements and compared with that of βCD. Considerable enhancement in the fluorescence intensity and lifetime of C7 on complexation with SBE7βCD proposes that non-radiative processes like TICT behavior are strictly hindered due to the confinement in the host cavity experienced by the C7 dye. The increase in the rotational correlation time evaluated from the fluorescence anisotropy decay kinetics further confirms the formation of tightly bound inclusion complexes. The binding constant values reveal that the monocationic form of dye at pH 3 shows ∼3 times stronger interaction with SBE7βCD than the neutral form of dye at pH 7 due to strong electrostatic cation-anion interaction. SBE7βCD:C7 exhibits an improved photostability and an upward pKa shift of 0.4 unit compared to the contrasting downward pKa shift of 0.5 with the βCD. The enhanced fluorescence yield and increased photostability have been exploited for bioimaging applications, and better images were captured by staining the Drosophila fly gut with the SBE7βCD:C7 complex. The enhancement in the binding interaction and the emission intensity were found to be responsive to external stimuli such as small competitive binders or metal ions and nearly quantitative dissociation of the complex was demonstrated to release the dye and would find stimuli-responsive applications.

Abstract The aqueous solution of ethylene glycol (EG) is a binary liquid mixture that displays rich conformational and structural behaviour, which has not yet been adequately explored through atomistic molecular dynamics simulations. Herein, employing an accurate force field for EG, several physical properties of this solution are calculated to be in quantitative agreement with experimental data. While 79 % of molecules in neat liquid EG exist with their central OCCO dihedral in the gauche state, this fraction increases to 89 % in the dilute aqueous solution, largely in response to the increase in the static dielectric constant of the solution from that of neat liquid EG. The increase in gauche conformers increases the mean dipole moment of EG molecules in the solution which is additionally contributed by specific conformational states of the two terminal HOCC dihedral angles.

Introduction: The Coronavirus Disease-2019 (COVID-19) pandemic has emerged from Wuhan, China in late 2019 and spread across the world in few months. This pandemic has affected people all over the world in terms of not only health but also psychologically, economically and socially. Early diagnosis by Real Time Polymerase Chain Reaction (RT-PCR) test helped the health system to isolate the patient and prevent the spread of the disease in community. Aim: To know the prevalence of asymptomatic COVID-19 infection among healthcare workers. Materials and Methods: This study was a cross-sectional study and focused on early detection of asymptomatic COVID19 infection among Healthcare Workers (HCW) by RT-PCR test. Total of 356 samples were collected of all HCW working in Nootan Medical College and Research Centre Visnagar, Gujarat, India, in month of May 2021. Data were analysed on basis of job profile, working area and vaccination status. Chi-square test was used for statistical analysis. Results: Out of total 356 samples, six were positive showing prevalence of 1.68%. Out of these six positive workers two had exposure to COVID-19 positive patients at home in last 10 days. No significance was found in positivity rate in relation to job profile, working area in hospital and vaccination status. Conclusion: This study reveals low prevalence of asymptomatic infection among HCWs engaged in COVID-19 related duties. The HCWs are at highest risk of contracting infection, hence it is necessary to protect their safety and health as infection among them can spread to other co-workers and patients.

Resistance against anti-tubercular drugs is a significant problem. This elucidates the need for novel drug targets. Altering and targeting the enzymes involved in cell wall synthesis led to fatal damage to the bacterial cell. Mycolic acids are critically responsible for the virulence of Mycobacterium Tuberculosis. This pathway represents an essential reservoir of novel targets for developing new TB drugs. The study aims to identify phytochemicals with the capacity to bind with enzymes of mycolic acid synthesis pathways. This study shows the interaction between phytochemicals and proteins responsible for mycolic acid synthesis is shown through bioinformatics & molecular docking tools. Docking showed binding affinity between protein molecules of the mycolic acid synthesis pathway and ligand molecules in the study. PKS13 (polyketide synthase) interacts with the ligand beta-amyrin acetate with a vina score of -7.1 Kcal/mol. At the same time, its binding energy with Piperine is -6.8 Kcal/mol. DprE1 (Decaprenylphosphoryl-bet-D-ribose-2-epimerase), the other protein docked with beta-amyrin acetate, showed a vina score of -9.7 Kcal/mol binding energy. Piperine with DprE1 exhibits interaction with a score of -8.3 Kcal/mol. Beta-amyrin acetate is docked with a score of -6.9 Kcal/mol against KasA (Beta-ketoacyl-acyl carrier protein synthase). On the other hand, Piperine with KasA gave a result of -7.0 Kcal/mol. Piperine and Beta-amyrin acetate binds to PKS13, DprE1 & KasA protein/enzymes responsible for mycolic acid biosynthesis.

Air quality networks in cities can be costly and inconsistent and typically monitor a few pollutants. Space-based instruments provide global coverage spanning more than a decade to determine trends in air quality, augmenting surface networks. Here we target cities in the UK (London and Birmingham) and India (Delhi and Kanpur) and use observations of nitrogen dioxide (NO2) from the Ozone Monitoring Instrument (OMI), ammonia (NH3) from the Infrared Atmospheric Sounding Interferometer (IASI), formaldehyde (HCHO) from OMI as a proxy for non-methane volatile organic compounds (NMVOCs), and aerosol optical depth (AOD) from the Moderate Resolution Imaging Spectroradiometer (MODIS) for PM2.5. We assess the skill of these products at reproducing monthly variability in surface concentrations of air pollutants where available. We find temporal consistency between column and surface NO2 in cities in the UK and India (R = 0.5–0.7) and NH3 at two of three rural sites in the UK (R = 0.5–0.7) but not between AOD and surface PM2.5 (R < 0.4). MODIS AOD is consistent with AERONET at sites in the UK and India (R ≥ 0.8) and reproduces a significant decline in surface PM2.5 in London (2.7 % a−1) and Birmingham (3.7 % a−1) since 2009. We derive long-term trends in the four cities for 2005–2018 from OMI and MODIS and for 2008–2018 from IASI. Trends of all pollutants are positive in Delhi, suggesting no air quality improvements there, despite the roll-out of controls on industrial and transport sectors. Kanpur, identified by the WHO as the most polluted city in the world in 2018, experiences a significant and substantial (3.1 % a−1) increase in PM2.5. The decline of NO2, NH3, and PM2.5 in London and Birmingham is likely due in large part to emissions controls on vehicles. Trends are significant only for NO2 and PM2.5. Reactive NMVOCs decline in Birmingham, but the trend is not significant. There is a recent (2012–2018) steep (> 9 % a−1) increase in reactive NMVOCs in London. The cause for this rapid increase is uncertain but may reflect the increased contribution of oxygenated volatile organic compounds (VOCs) from household products, the food and beverage industry, and domestic wood burning, with implications for the formation of ozone in a VOC-limited city.

Tailored reaction of Schiff base ligands with palladium(II) chloride and imidazole afford three complexes of formula [Pd(II)(L)(imdz)2]Cl, which are L = 2-((E)-(p-lylimino)methyl)-6-methoxyphenol (complex 1), 2-methoxy- -6-((E)-(phenylimine)methyl)phenol (complex 2) and 2-((E)-(4-chlorophenylimino) methyl)-6-methoxyphenol (complex 3). Compounds were characterized with elemental analysis, molar conductance, electronic spectroscopy, ESI-MS, FT-IR, TGA, 1H-NMR and 13C-NMR. Molecular structure and different quantum chemical parameters were calculated using the B3LYP basis set of density functional theory with the standard 6-311+G (d, 2p) level. The catalytic potential of 1-3 was examined over Heck-Mizoroki reaction and found in order of 1 > 2 > 3.

The Schiff base ligand, namely (7E)-N-benzylidene-2-styrylbenzenamine- 1,2-diamine-2,4-dihydroxy-phenol (L), was synthesized by condensation of 2,4-dihydroxybenzaldehyde with o-phenylenediamine. The reaction of the ligand with Fe(III), Co(II) and Ni(II) salts in an 1:1 ratio yielded three complexes (1–3). Different analytical tools, like elemental analysis, ESI-MS, UV–Vis, FT-IR, NMR and EPR spectroscopy, then molar conductivity and magnetic susceptibility spectra, were used to elucidate the structure of the ligand and complexes. Density functional theory calculation at the B3LYP/3- -211G++/LANL2DZ level of the theory has been carried out to optimize the geometry of the ligand and complexes. The tetradentate ligand has coordinated to metals through ONNO donors affording octahedral geometry. Complexes were studied for their oxygen-binding activity and free radical scavenging activities. Complexes 1 and 2, which contain Fe(IIl) and Co(II), displayed reversible oxygen binding activity. On the other hand, complex 3 fails to show oxygen binding. The order of antioxidant activity is: 3 > 1 > 2 > L.

To obtain high performance, generalization, and accuracy in machine learning applications, such as prediction or anomaly detection, large datasets are a necessary prerequisite. Moreover, the collection of data is time-consuming, difficult, and expensive for many imbalanced or small datasets. These challenges are evident in collecting data for financial and banking services, pharmaceuticals and healthcare, manufacturing and the automobile, robotics car, sensor time-series data, and many more. To overcome the challenges of data collection, researchers in many domains are becoming more and more interested in the development or generation of synthetic data. Generating synthetic time-series data is far more complicated and expensive than generating synthetic tabular data. The primary objective of the paper is to generate multivariate time-series data (for continuous and mixed parameters) that are comparable and evaluated with real multivariate time-series synthetic data. After being trained to produce such data, a novel GAN architecture named as MTS-TGAN is proposed and then assessed using both qualitative measures namely t-SNE, PCA, discriminative and predictive scores as well as quantitative measures, for which an RNN model is implemented, which calculates MAE and MSLE scores for three training phases; Train Real Test Real, Train Real Test Synthetic and Train Synthetic Test Real. The model is able to reduce the overall error up to 13% and 10% in predictive and discriminative scores, respectively. The research’s objectives are met, and the outcomes demonstrate that MTS-TGAN is able to pick up on the distribution and underlying knowledge included in the attributes of the real data and it can serve as a starting point for additional research in the respective area.

A highly efficient magnetically separable copper nanocatalyst has been developed for decarboxylative cross-coupling reaction for the alkynylation of haloarenes using alkynoic acid as a reaction partner. The chemical nature, morphology, size, and magnetic properties of the prepared nanocatalyst were studied by SEM, TEM, EDS, FT-IR, VSM, and ICP techniques. Remarkably, this catalyst represents the first successful copper based heterogeneous system for this type of coupling that provides a low-cost, stable, and environmentally friendly magnetically recoverable entity that can be re-used for seven consecutive runs without appreciable loss in its catalytic performance.

In recent years, due to its high hole-mobility, high on/off current ratio and low threshold voltage, pentacene and its derivatives have found increasing application in the fabrication of light-emitting diodes, field-effect transistors and photovoltaic cells. It has also emerged as an alternative to silicon due to its similar performance to inorganic semiconductors. Pentacene cannot be isolated from the petroleum fractions like other acenes such as anthracene or tetracene, and therefore it needs to be chemically synthesized. The first successful synthesis of pentacene was reported in early 19th century where pentacene was obtained via dehydrogenation of 6,14-dihydropentacene. Since then a number of methods have been reported for the synthesis of pentacene. This review describes various strategies used for the synthesis of pentacene and its derivatives reported since 2005. Keywords: Pentacene, Synthesis, Semi-conductor, Aromatic compounds, Acenes

The present study reported the synthesis of SnS2 nanoparticles by using a thermal decomposition approach using tin chloride and thioacetamide in diphenyl ether at 200 °C over 60 min. SnS2 nanoparticles with novel morphologies were prepared by the use of different alkylamines (namely, octylamine (OCA), dodecylamine (DDA), and oleylamine (OLA)), and their role during the synthesis was explored in detail. The synthesized SnS2 nanostructures were characterized using an array of analytical techniques. The XRD results confirmed the formation of hexagonal SnS2, and the crystallite size varied from 6.1 nm to 19.0 nm and from 2.5 to 8.8 nm for (100) and (011) reflections, respectively. The functional group and thermal analysis confirmed the presence of organics on the surface of nanoparticles. The FE-SEM results revealed nanoparticles, nanoplates, and flakes assembled into flower-like morphologies when dodecylamine, octylamine, and oleylamine were used as capping agents, respectively. The analysis of optical properties showed the variation in the bandgap and the concentration of surface defects on the SnS2 nanoparticles. The role of alkylamine as a capping agent was explored and discussed in detail in this paper and the mechanism for the evolution of different morphologies of SnS2 nanoparticles was also proposed.

All humans and animals need access to clean water in their daily lives. Unfortunately, we are facing water scarcity in several places around the world, and, intentionally or unintentionally, we are contaminating the water in a number of ways. The rise in population, globalization, and industrialization has simultaneously given rise to the generation of wastewater. The pollutants in wastewater, such as organic contaminants, heavy metals, agrochemicals, radioactive pollutants, etc., can cause various ailments as well as environmental damage. In addition to the existing pollutants, a number of new pollutants are now being produced by developing industries. To address this issue, we require some emerging tools and materials to remove effluents from wastewater. Zeolites are the porous aluminosilicates that have been used for the effective pollutant removal for a long time owing to their extraordinary adsorption and ion-exchange properties, which make them available for the removal of a variety of contaminants. However, zeolite alone shows much less photocatalytic efficiency, therefore, different photoactive materials are being doped with zeolites to enhance their photocatalytic efficiency. The fabrication of zeolite-based composites is emerging due to their powerful results as adsorbents, ion-exchangers, and additional benefits as good photocatalysts. This review highlights the types, synthesis and removal mechanisms of zeolite-based materials for wastewater treatment with the basic knowledge about zeolites and wastewater along with the research gaps, which gives a quality background of worldwide research on this topic for future developments.

Nanomaterials are materials with one or more nanoscale dimensions (internal or external) (i.e., 1 to 100 nm). The nanomaterial shape, size, porosity, surface chemistry, and composition are controlled at the nanoscale, and this offers interesting properties compared with bulk materials. This review describes how nanomaterials are classified, their fabrication, functionalization techniques, and growth-controlled mechanisms. First, the history of nanomaterials is summarized and then the different classification methods, based on their dimensionality (0–3D), composition (carbon, inorganic, organic, and hybrids), origin (natural, incidental, engineered, bioinspired), crystal phase (single phase, multiphase), and dispersion state (dispersed or aggregated), are presented. Then, the synthesis methods are discussed and classified in function of the starting material (bottom-up and top-down), reaction phase (gas, plasma, liquid, and solid), and nature of the dispersing forces (mechanical, physical, chemical, physicochemical, and biological). Finally, the challenges in synthesizing nanomaterials for research and commercial use are highlighted.

Water is a vital resource that is required for social and economic development. A rapid increase in industrialization and numerous anthropogenic activities have resulted in severe water contamination. In particular, the contamination caused by heavy metal discharge has a negative impact on human health and the aquatic environment due to the non-biodegradability, toxicity, and carcinogenic effects of heavy metals. Thus, there is an immediate need to recycle wastewater before releasing heavy metals into water bodies. Hydrogels, as potent adsorbent materials, are a good contenders for treating toxic heavy metals in wastewater. Hydrogels are a soft matter formed via the cross-linking of natural or synthetic polymers to develop a three-dimensional mesh structure. The inherent properties of hydrogels, such as biodegradability, swell-ability, and functionalization, have made them superior applications for heavy metal removal. In this review, we have emphasized the recent development in the synthesis of hydrogel-based adsorbent materials. The review starts with a discussion on the methods used for recycling wastewater. The discussion then shifts to properties, classification based on various criteria, and surface functionality. In addition, the synthesis and adsorption mechanisms are explained in detail with the understanding of the regeneration, recovery, and reuse of hydrogel-based adsorbent materials. Therefore, the cost-effective, facile, easy to modify and biodegradable hydrogel may provide a long-term solution for heavy metal removal.

In the last few decades, the vast potential of nanomaterials for biomedical and healthcare applications has been extensively investigated. Several case studies demonstrated that nanomaterials can offer solutions to the current challenges of raw materials in the biomedical and healthcare fields. This review describes the different nanoparticles and nanostructured material synthesis approaches and presents some emerging biomedical, healthcare, and agro-food applications. This review focuses on various nanomaterial types (e.g., spherical, nanorods, nanotubes, nanosheets, nanofibers, core-shell, and mesoporous) that can be synthesized from different raw materials and their emerging applications in bioimaging, biosensing, drug delivery, tissue engineering, antimicrobial, and agro-foods. Depending on their morphology (e.g., size, aspect ratio, geometry, porosity), nanomaterials can be used as formulation modifiers, moisturizers, nanofillers, additives, membranes, and films. As toxicological assessment depends on sizes and morphologies, stringent regulation is needed from the testing of efficient nanomaterials dosages. The challenges and perspectives for an industrial breakthrough of nanomaterials are related to the optimization of production and processing conditions.

A mild and efficient catalytic method has been developed to synthesize 3,4-dihydropyrimidinones in high yield by one-pot three component Biginelli condensation in the presence of triethylammonium acetate (TEAA) which acts as catalyst/reaction medium. Further, we have studied the antioxidant and antibacterial activities of these synthesized 3,4-dihydropyrimidinones. All the synthesized compounds reveal the significant antioxidant properties, these properties have been studied using 1,1-diphenyl-2-picrylhydrazyl (DPPH) free radical scavenging and cupric reducing antioxidant capacity (CUPRAC) assays. In addition, to this, these compounds also show the good antibacterial activity against four human pathogenic bacteria.

With the rapid growth in population and economic development, emissions of greenhouse gases (GHGs) from the Indian subcontinent have sharply increased during recent decades. However, evaluation of regional fluxes of GHGs and characterization of their spatial and temporal variations by atmospheric inversions remain uncertain due to a sparse regional atmospheric observation network. As a result of an Indo-French collaboration, three new atmospheric stations were established in India at Hanle (HLE), Pondicherry (PON) and Port Blair (PBL), with the objective of monitoring the atmospheric concentrations of GHGs and other trace gases. Here we present the results of the measurements of CO2, CH4, N2O, SF6, CO, and H2 from regular flask sampling at these three stations over the period 2007–2011. For each species, annual means, seasonal cycles and gradients between stations were calculated and related to variations in natural GHG fluxes, anthropogenic emissions, and monsoon circulations. Covariances between species at the synoptic scale were analyzed to investigate the likely source(s) of emissions. The flask measurements of various trace gases at the three stations have the potential to constrain the inversions of fluxes over southern and northeastern India. However, this network of ground stations needs further extension to other parts of India to better constrain the GHG budgets at regional and continental scales.

Vinyl ester resin (VEOCN) was prepared from o-cresol epoxy resin (EOCN) and methacrylic acid in the presence of triphenyl phosphine as catalyst and hydroquinone as inhibitor with acid value of ~ 7 mg of KOH per gram of solid. O-cresol based novolac resin (OCN), OCN based epoxy resin (EOCN) and VEOCN were characterized by Fourier transform infra red spectroscopy (FT-IR), 1H-NMR and 13C-NMR. The thermal and mechanical behavior of the samples prepared at 30°C from VEOCN using styrene and methyl-methacrylate respectively as reactive diluents, in the presence of benzoyl peroxide (2 phr) as initiator was studied using Differential Scanning Calorimetry (DSC), Thermogravimetric analysis (TGA) and Universal Testing Machine (UTM). Chemical resistance of above VER samples was also evaluated as a function of % weight loss and with the help of Scanning Electron Microscopy (SEM), upon immersing the VEOCN samples in different solutions for 90 days.

Sulfonated poly (arylene ether sulfone) membranes were synthesized by direct copolymerization of 4,4-bis (4-hydroxyphenyl) valeric acid, 4,4′-difluorodiphenyl sulfone and synthesized sulfonated 6F-bisphenol-A/bisphenol-A as novel proton exchange membranes for fuel cell applications. Prepared membranes were subsequently crosslinked with synthesized 6F-bisphenol-A based epoxy resin (EFN) by thermal curing reaction keeping in view the resilience and toughness of the membranes. The structural characterization was done by using Fourier transform infrared (FTIR), 1H nuclear magnetic resonance (NMR) and 13C NMR techniques. Proton conductivity of the membranes was determined by a four-point probe technique. Methanol permeability was determined by using a diffusion cell in which concentration of the liquids was determined by UV-spectroscopic technique. The enhancement in mechanical properties determined by a universal testing machine and also a better oxidative stability were observed for the crosslinked membranes. However, a decrease in their water and methanol absorption, ion exchange capacity, proton conductivity and methanol permeability was observed. This was due to the reduction in the numbers of ionic channels in case of crosslinked membranes which was confirmed by carrying out morphological analysis of the membranes using atomic force microscopy. In addition, X-ray diffraction measurement by XPERT-PRO diffractometer was also used for structural characterization. Crosslinked membranes showed better thermal stability as determined by thermogravimetric analysis and differential scanning calorimetry.

Methacrylated lignin model compounds (LMCs, i.e., eugenol and guaiacol) monomers are ideal candidates as styrene replacements because they have low volatilities and can free-radically polymerize with vinyl ester resins. This article reports the synthesis of methacrylated eugenol (ME), methacrylated guaiacol (MG) using LMCs and methacrylic anhydride in the presence of 4-dimethylaminopyridine (DMAP) as a catalyst. ME and MG were characterized using FT-IR, 1H-NMR and 13C-NMR. The thermal and mechanical properties of the samples prepared at 30°C from o-cresol epoxy based vinyl ester resin (VEOCN) using MG and ME, respectively, as reactive monomers, in the presence of benzoyl peroxide (2 phr) as initiator were further investigated using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA/DTG/DTA) and universal testing machine (UTM). Chemical and corrosion resistance of cured VEOCN samples coated on steel panels were also evaluated as a function of percentage weight loss and with the help of scanning electron microscopy (SEM), upon immersing the VEOCN samples in 1 m HCl, 1 m NaOH and 1 m NaCl solutions for 90 days. Thermal, mechanical and chemical performance of VEOCN using ME and MG was also compared with VEOCN samples containing styrene and methyl methacrylate (MMA) as reactive monomers.

In this study, a dinucleating spacer incorporating two 2-aminopyridine units has been used to prepare seven novel dinuclear compounds. These molecules were characterized by elemental analyses, conductivity measurements, magnetic susceptibility, FT-IR, FAB-Mass, electronic, 1H and 13C{1H}NMR spectral studies. The complex [{trans,mer-RuCl2(DMSO)3}2(μ-5,5'-methylenebis(2-aminopyridine))].2DMSO, 2 was also characterized through 1H-1H COSY NMR. There are mainly three different formulations; [{cis,fac-RuCl2(SO)3}2(μ-MBAP)].2SO; [{trans,mer-RuCl2(SO)3}2(μ-MBAP)].2SO and [{trans-RuCl4(SO)}2(μ-MBAP)]2- [X]2+; where SO = DMSO / TMSO; MBAP = 5,5'-methylenebis(2-aminopyridine) and [X]+ = [(DMSO)2H]+, Na+ or [(TMSO)H]+. The coordination was found through cyclic nitrogen of pyridine ring in octahedral environment for both metal centers. The chemical behivour of [{cis,fac-RuCl2(DMSO)3}2(μ-5,5'-methylenebis(2-aminopyridine))].2DMSO, 1 and 2 in aqueous solution with respect to time was observed by conductivity measurements and UV-vis spectrophotometer. All complexes were found to possess prominent antibacterial activity against Escherichia coli in comparison to Chloramphenicol and Gatifloxacin.