Structural and optical properties of silver supported α-Fe2O3 nanocomposite fabricated by Saraca asoca leaf extract for the effective photo-degradation of cationic dye Azure B.

In recent decades, several nanocomposites developed by chemical synthetic routes, have been demonstrated as efficient photocatalysts for the photodegradation of hazardous organic dyes. The present investigation reports the sonochemical-assisted fabrication of silver-supported α-Fe2O3 nanocomposites (SA@Ag@IONCs) using the Saraca asoca leaf extract. The magnetic nanocomposites can be easily removed from the reaction mixture. The morphology of these materials was characterized by field emission scanning electron microscopy (FESEM), high-resolution transmission electron microscopy (HRTEM), XPS, BET surface area analyzer, UV-visible spectroscopy, photoluminescence, X-ray diffraction (XRD), and VSM techniques. The XRD and electron microscopy analyses revealed the small size and well-crystalline SA@Ag@IONC particles with spherical and buckyball structures. The large surface area of SA@Ag@IONCs was confirmed by BET analysis. The absorption edge in UV-visible spectra appeared to migrate towards high wavelengths for the SA@Ag@IONC composite, causing a change in the bandgap energy. In the case of the sonication assisted composite, the bandgap energy was 2.1 eV, making it easier for the electron to transfer from the valence band to conduction band. The decoration of ultrasmall silver onto the surfaces of the α-Fe2O3 nanocomposite, which considerably increases the capacity to absorb sunlight, enhances the efficiency of charge carrier separation, and inhibits the electron-hole recombination rate as confirmed by the reduced PL intensity, is responsible for the excellent photocatalytic degradation performance. Outcomes shown SA@Ag@IONCs have a high photodegradation rate as well as high-rate constant value at an optimized condition that is at pH 9 and 0.5 g L-1 dose of nanocomposite, photodegradation rate of Azure B is ∼94%. Trap experiment results indicated that O2˙- and h+ are the active species responsible for the photodegradation of AzB.

Biosynthesis of ZnO and TiO2 nanoparticles using Ipomoea carnea leaf extract and its effect on black carrot (Daucus carota L.) cv. Pusa Asita.

Nano fertilizers (NFs) are now becoming an important tool for plant nutrient management having capabilities to improve soil fertility, crop productivity and quality of agricultural products. Since, they are needed in very small amount, thus, reduces cost of crop production. Among different essential or beneficial plant nutrients, Zn and Ti are important micro nutrients having number of beneficial effect on crop growth, yield, quality and post harvest life. Present experiment was carried out to prepare ZnO and TiO2 nanoparticles (NPs) through green technology by using aqueous extract of Ipomoea carnea (morning glory) leaves. In order to investigate size, morphology, composition, and stability of selected NPs, the detailed characterization was carried out using UV-visible spectroscopy, FTIR, HRTEM, EDX, BET, X-ray diffraction, XPS and particle size distribution studies. Subsequently, the effect of foliar spray of ZnO and TiO2 NPs was evaluated in respect of vegetative growth, yield and quality of black carrot (Daucus carota L.) cv. Pusa Asita in presence of 50% Recommended dose of fertilizer (RDF) to assess their effect on fertilizer use efficiency also. There were 8 treatments viz. Control (no fertilizer), recommended dose of fertilizer (RDF), TiO2 (5, 10 and 15 ppm along with 50% RDF), ZnO (50, 75 and 100 ppm along with 50% RDF)] with 3 replications following Randomised Block Design having 24 plots (1 m × 1 m). The observations were taken for vegetative growth, edible root yield and root quality parameters. Although, the growth, yield and quality parameters were found superior (root yield 43.84 g/plant) under conventional system of recommended dose of fertilizers (RDF) of NPK, however, TiO2 NPs also showed very promising result close to RDF as compared to ZnO NPs. Among them, 5 ppm TiO2 foliar application along with 50% NPK was found to be the best in terms of vegetative growth, root yield (38.73 g/plant) and quality of black carrot. It was also found that higher concentration of TiO2 and ZnO NPs had adverse effect on the plant performance. Therefore, it can be concluded that 5 ppm TiO2 NPs along with 50% RDF was good for black carrot production.

Retraction of "Effect of Reaction Temperature on Shape Evolution of Palladium Nanoparticles and Their Cytotoxicity against A-549 Lung Cancer Cells".

[This retracts the article DOI: 10.1021/acsomega.9b02776.].

Retraction of "One-Pot Surface Modification of ß-Cu2O NPs for Biocatalytic Performance against A-549 Lung Carcinoma Cell Lines through Docking Analysis".

[This retracts the article DOI: 10.1021/acsomega.1c02942.].

One-Pot Surface Modification of ß-Cu2O NPs for Biocatalytic Performance against A-549 Lung Carcinoma Cell Lines through Docking Analysis.

The physicochemical approaches and biological principles in bio-nanotechnology favor specially functionalized nanosized particles. Cuprous oxide nanoparticles (ß-Cu2O NPs) of cuprite phase with a little tenorite (CuO) may be very effective in the development of novel therapeutic approaches against several fatalities including A-549 lung carcinoma cell lines. Consequently, the synthesis of ß-Cu2O NPs for the improvement in the therapeutic index and drug delivery application is becoming an effective strategy in conventional anticarcinoma treatment. Hence, surface-enhanced nanosized spherical cuprous oxide nanoparticles (ß-Cu2O NPs) of cuprite phase were successfully prepared using poly(ethylene glycol) (PEG) as an amphiphilic nonionic surfactant and l-ascorbic acid (K3[Cu(Cl5)]@LAA-PEG) reduced to cuprites ß-Cu2O NPs via the sonochemical route. Less improved toxicity and better solubility of ß-Cu2O NPs compared with Axitinib were a major reason for producing ß-Cu2O NPs from K3[Cu(Cl5)]@LAA-PEG (LAA, l-ascorbic acid, PEG, poly(ethylene glycol) (PEG)). These nanoparticle syntheses have been suggested to influence their cytotoxicity, free-radical scavenging analysis, and reactive oxygen species (ROS) using poly(ethylene glycol) (PEG) and l-ascorbic acid (LAA) as coated and grafted materials due to their dose-dependent nature and IC50 calculations. The surface morphology of the formed ß-Cu2O NPs has been examined via UV-vis spectroscopy, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy with energy diffraction scattering spectroscopy (SEM@EDS), field emission scanning electron microscopy (FESEM), and transmission electron microscopy (TEM) analysis. X-ray diffraction (XRD) and Brunauer-Emmett-Teller (BET) surface analysis results confirm the presence of pure cuprite with a very little amount of tenorite (CuO) phase, Dynamic light scattering (DLS) confirms the negative ζ-value with stable nature. Docking was performed using PDB of lung carcinomas and others, as rigid receptors, whereas the ß-Cu2O NP cluster was treated as a flexible ligand.

Meta Selective C-H Borylation of Sterically Biased and Unbiased Substrates Directed by Electrostatic Interaction.

An electrostatically directed meta borylation of sterically biased and unbiased substrates is described. The borylation follows an electrostatic interaction between the partially positive and negative charges between the ligand and substrate. With this strategy, it has been demonstrated that a wide number of challenging substrates, especially 4-substituted substrates, can selectively be borylated at the meta position. Moreover, unsubstituted substrates also displayed excellent meta selectivity. The reaction employs a bench-stable ligand and proceeds at a milder temperature, precluding the need to synthesize a bulky and sophisticated ligand/template.

Double-Fold Ortho and Remote C-H Bond Activation/Borylation of BINOL: A Unified Strategy for Arylation of BINOL.

A double-fold ortho and remote C-H borylation of BINOL is described. The proposed mechanisms involved electrostatically and sterically directed ortho and remote C-H activation processes, respectively. While B2eg2 (eg = ethylene glycolate) directs the C-H activation at ortho positions, a combination of HBpin and B2pin2 activates remote C-H bonds. The strategy was combined with Suzuki arylation as a one-pot protocol for the rapid synthesis of BINOL derivatives with retention of chirality.

Nitrogen donor ligand for capping ZnS quantum dots: a quantum chemical and toxicological insight.

Nanoparticles having strong optical and electronic properties are the most widely used materials in sensor development. Since the target analyte interacts directly with the surface of the material, the choice of ligand for functionalizing the surface of the material is the key for its further applications. The functionalized surface of the material makes it suitable for required applications as it controls the size of the particle during its growth from the solution phase. Biomolecule capped nanomaterials are favourable for various applications in bio-sensing. In the present work, an attempt has been made to explore the biologically active molecule imidazole as capping agent for ZnS semiconductor nanoparticles or quantum dots (QDs). This work explores the possibility of replacing conventional thiol-zinc bonding and hence paves new pathways for biomolecules having the possibility of being efficient capping agents. Computational chemistry has been used to study the mechanism of bonding between one of the nitrogen atoms of imidazole and the zinc ion of the ZnS QDs. The quantum chemical insight not only explores the most spontaneous interaction of zinc ion and imidazole molecule so as to act as an efficient capping agent but also explains the probable bonding site for nitrogen-zinc chemistry. The tailormade Mn doped ZnS QDs are one of the most promising materials for probe and sensor development. The ZnS core having non-toxicity and the emission in longer wavelength due to manganese makes this material highly useful biologically. The aqueous route of synthesis has been employed to obtain a highly homogeneous and pure material which was further characterized by UV (Ultra Violet spectroscopy), Spectrofluorometer, Transmission Electron Microscope and X-ray Diffraction. The toxicity at the cellular and genetic levels was also investigated to prove the potential of the imidazole capped Mn doped ZnS QD as a biocompatible material.

Effect of Reaction Temperature on Shape Evolution of Palladium Nanoparticles and Their Cytotoxicity against A-549 Lung Cancer Cells.

Palladium nanoparticles (Pd NPs) of different shapes and sizes have been synthesized by reducing potassium tetrachloropalladinate(II) by l-ascorbic acid (AA) in an aqueous solution phase in the presence of an amphiphilic nonionic surfactant poly ethylene glycol (PEG) via a sonochemical method. Materials have been characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray soectrscopy (EDX), Fourier transform infrared (FTIR), surface-enhanced Raman spectroscopy (SERS), particle distribution, and zeta potential studies. Truncated octahedron/fivefold twinned pentagonal rods are formed at room temperature (RT) (25 °C) while hexagonal/trigonal plates are formed at 65 °C. XRD results show evolution of anisotropically grown, phase-pure, and well crystalline face-centered cubic Pd NPs at both temperatures. FTIR and SERS studies revealed adsorption of ascorbic acid (AA) and PEG at NP's surface. Particle's size distribution graph indicates formation of particles having wide size distribution while the zeta potential particle surface is negatively charged and stable. The truncated octahedron/fivefold twinned pentagonal rod-shaped Pd NPs, formed at RT, while thermally stable and kinetically controlled hexagonal/trigonal plate-like Pd NPs, evolved at higher temperature 65 °C. The obtained Pd NPs have a high surface area and narrow pore size distribution. To predict protein reactivity of the Pd cluster, docking has been done with DNA and lung cancer-effective proteins. The cytotoxicity of the Pd NPs has been screened on human lung cancer cells A-549 at 37 °C. The biological adaptability exhibited by Pd NPs has opened a pathway in biochemical applications.

Achieving High Ortho Selectivity in Aniline C-H Borylations by Modifying Boron Substituents.

High ortho selectivity for Ir-catalyzed C-H borylations (CHBs) of anilines results when B2eg2 (eg = ethylene glycolate) is used as the borylating reagent in lieu of B2pin2, which is known to give isomeric mixtures with anilines lacking a blocking group at the 4-position. With this modification, high selectivities and good yields are now possible for various anilines, including those with groups at the 2- and 3-positions. Experiments indicate that ArylN(H)Beg species are generated prior to CHB and support the improved ortho selectivity relative to B2pin2 reactions arising from smaller Beg ligands on the Ir catalyst. The lowest-energy transition states (TSs) from density functional theory computational analyses have N-H···O hydrogen-bonding interactions between PhN(H)Beg and O atoms in Beg ligands. Ir-catalyzed CHB of PhN(H)Me with B2eg2 is also highly ortho-selective. 1H NMR experiments show that N-borylation fully generates PhN(Me)Beg prior to CHB. The TS with the lowest Gibbs energy was the ortho TS, in which the Beg unit is oriented anti to the bipyridine ligand.

A ternary Fe(ii)-terpyridyl complex-based single platform for reversible multiple-ion recognition.

Multiple ion-recognition activity by a ternary Fe(ii)-terpyridyl complex, [Fe(PhT)(PT)]2+ (1) (PhT = 4'-phenyl-2,2':6',2''-terpyridine; PT = 4'-pyridyl-2,2':6',2''-terpyridine), is demonstrated for cyanide (CN-), fluoride (F-) and hydroxide (OH-) ions in an aqueous medium with sufficient sensitivity, fast response, reproducibility and selectivity with a dual optical read-out. The sensing event was reversible with the "by-eye" visualization of back and forth colour changes. Three cyanide ions replaced PT from 1, as observed from the crystal structure of the 1 + CN- couple. Fluoride and hydroxide ions appeared to show multivariate interactions with 1. Observed structural and spectral changes correlated well with theoretical calculations. A string of cations at quantitative levels (Ag+/Hg2+/Fe2+/Fe3+) was used to decouple the 1 + anion complex to yield 1, which enabled the recognition of these cations while permitting the reuse of 1 for at least five set-reset cycles.

Nucleation temperature-controlled synthesis and in vitro toxicity evaluation of L-cysteine-capped Mn:ZnS quantum dots for intracellular imaging.

Quantum dots (QDs), one of the fastest developing and most exciting fluorescent materials, have attracted increasing interest in bioimaging and biomedical applications. The long-term stability and emission in the visible region of QDs have proved their applicability as a significant fluorophore in cell labelling. In this study, an attempt has been made to explore the efficacy of L-cysteine as a capping agent for Mn-doped ZnS QD for intracellular imaging. A room temperature nucleation strategy was adopted to prepare non-toxic, water-dispersible and biocompatible Mn:ZnS QDs. Aqueous and room temperature QDs with L-cysteine as a capping agent were found to be non-toxic even at a concentration of 1500 µg/mL and have wide applications in intracellular imaging.

Synthesis, characterization, spectral studies and antifungal activity of Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and Zn(II) complexes with 2-(4- sulphophenylazo)-1,8-dihydroxy-3,6-napthalene disulphonic acid trisodium salt.

Complexes of the type Na(6)[M(HL)(2)(H(2)O)(2)], where M= Mn(II), Fe(II), Co(II), Ni(II), Cu(II) and Zn(II) and Na(3)H(2)L= 2-(4-sulphophenylazo)-1,8-dihydroxy 3,6 naphthalene disulphonic acid trisodium salt, have been synthesized and characterized by physico-chemical (elemental analyses, solubility, electrolytic conductance, magnetic susceptibility measurement) and spectral (UV-Visible, IR, ESR, powder x-ray diffraction) techniques for their structure and studied for their antifungal activity against ten fungi. The anionic 1:2 metal:ligand complexes show octahedral geometry around M(II), a significant antifungal activity against Curvularia lunata and Alternaria triticina and a moderate activity against Alternaria brassicicola, Alternaria brassicae, Alternaria solanae, Curvularia species, Helminthosporium oryzae, Collectotrichum capsici, Aspergillus niger, Aspergillus flavus and Fusarium udum.