Photoluminescent and photocatalytic behaviour of zinc oxide nanostructures synthesized through the room temperature ultrasonication method.

In the present article we report the synthesis of zinc oxide (ZnO) nanostructures at room temperature using an ultrasonication technique to study their photoluminescent and photocatalytic behaviour. Synthesized nanomaterial showed a strong near band edge ultraviolet (UV) light emission and red emission, thereby finding its use in photoluminescent materials. We developed a UV/ZnO/O2 /H2 O2 system for the photodegradation of organic pollutants in an aqueous system. We used synthesized nanostructures to photodegrade phenol red (PR) dye to check their photocatalytic activity. The ZnO nanostructures photodegraded more than 90% of the PR dye under UV light irradiation in which photonic energy is converted to chemical energy (photocatalytic energy conversion), thereby exploitable for water purification applications. Synthesized ZnO nanostructures were characterized using powder X-ray diffraction, Fourier transform infrared spectroscopy, UV-visible light spectroscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy to investigate their structural, optical, morphological, and compositional properties, respectively.

Hydrothermally grown Cu doped NiMnO3 perovskite nanostructures suitable for optoelectronic, photoluminescent and electrochemical properties.

Transition metal-based perovskites have emerged as highly promising and economically advantageous semiconductor materials due to their exceptional performance in optoelectronics, photovoltaic, photocatalysis, and photoluminescence. In this study, we employed a microwave-assisted hydrothermal process to produce a Cu-doped NiMnO3 nanocomposite electrode material. The appearance of a peak corresponding to the (110) plane with a 2θ value of 36.6° confirmed the growth of the rhombohedral NiMnO3 crystal structure. The presence of metal-oxygen bonds in NiMnO3 was confirmed through FTIR spectra. XPS validates the chemical composition, providing additional support for the results obtained from XRD and FT-IR analyses. FE-SEM affirmed the anisotropic growth of small sphere-like structures that agglomerated to form broccoli-like shapes. Cu doping modified the band gap, reducing it from 2.2 to 1.7 eV and enhancing its photoluminescent (PL) activity by introducing defects. The increase in PL intensity (visible light luminescent intensity) can be attributed to a concurrent rise in complex defects and the rate of recombination of electron-hole pairs. Finally, the electrochemical activity demonstrated the pseudo-capacitor behavior of the synthesized material, with capacitance values increasing as the copper (Cu) content in the parent lattice increased.

Photoluminescence Emission Studies on a Lanthanum-Doped Lead Free Double Halide Perovskite, La:Cs2SnCl6.

Recent advances in bandgap engineering have increased the possibility of vacancy ordered double halide perovskites (VO-DHPs), Cs2SnX6 where X = Cl, Br, I with designable optoelectronic features. Doping with La3+ ions modulates the band gap from 3.8 to 2.7 eV, allowing a steady room temperature dual emission (PL) centered at 440 and 705 nm in Cs2SnCl6. Pristine Cs2SnCl6 and La:Cs2SnCl6 both have a crystalline cubic structure with a space symmetry of Fm3m. The cubic phase correlates well with the Rietveld refinement. SEM analysis confirms anisotropic development with huge micrometer-sized (>10 µm) truncated octahedral structures. DFT investigations show that the insertion of La3+ ions into the crystal lattice leads to the band splitting. The present study elaborates the experimental understanding of the dual PL emission properties of La:Cs2SnCl6 leaving a scope for detailed theoretical study on the origin of the complex electronic transitions involving f-orbital electrons.

Synthesis of 1,5-benzodiazepine and its derivatives by condensation reaction using H-MCM-22 as catalyst.

A simple and versatile method for the synthesis of 1,5-benzodiazepines is via condensation of o-phenylenediamines (OPDA) and ketones in the presence of catalytic amount of H-MCM-22 using acetonitrile as solvent at room temperature. In all the cases, the reactions are highly selective and are completed within 1-3 h. The method is applicable to both cyclic and acyclic ketones without significant differences. The reaction proceeds efficiently under ambient conditions with good-to-excellent yields.

Growth of crystalline WO3-ZnSe nanocomposites: an approach to optical, electrochemical, and catalytic properties.

In this study, novel growth of WO3-ZnSe nanocomposites was carried out by a simple, low-cost hydrothermal process under subcritical conditions and is reported for the first time in just 5 h. The products were characterized in detail by multiform techniques: X-ray diffraction, scanning electron microscopy (SEM), optical studies, and Fourier transform analysis. The influence of ZnSe on the structural, morphological, compositional, optical, and catalytic properties of WO3 is demonstrated. The WO3 metal oxide material is grown in a hexagonal crystal structure with wide-band-gap and has been modified by ZnSe to form a composite nanostructures in the nanoscale range. The electrochemical properties of the prepared materials were studied by cyclic voltammetry, which revealed that the synthesized material exhibited remarkable electrochemical supercapacitive activity. Moreover, the composite nanostructures showed excellent photocatalytic activity for degradation of phenol and almost 93% of phenol was degraded with good recyclability and stability. According to The International Commission on Illumination (CIE), the synthesized nanomaterial shows blue emission and is suitable for blue LEDs.

Diastereoselective palladium-catalyzed functionalization of prochiral C(sp3)-H bonds of aliphatic and alicyclic compounds.

We highlight the reported developments of the palladium-catalyzed C-H activation and functionalization of the inactive/unreactive prochiral C(sp3)-H bonds of aliphatic and alicyclic compounds. There exist numerous classical methods for generating contiguous stereogenic centers in a compound with a high degree of stereocontrol. Along similar lines, the Pd(II)-catalyzed, directing group-aided functionalization of inactive prochiral/diastereotopic C(sp3)-H bonds have been exploited to accomplish the stereoselective construction of stereo-arrays in organic compounds. We present a concise discussion on how specific strategies consisting of Pd(II)-catalyzed, directing group-aided C(sp3)-H functionalization have been utilized to generate two or more stereogenic centers in aliphatic and alicyclic compounds.

Azobenzene-based unnatural amino acid scaffolds via a Pd(II)-catalyzed C(sp3)-H arylation strategy.

Azobenzene-based unnatural amino acid motifs were synthesized via Pd(II)-catalyzed diastereoselective C(sp3)-H arylation of amino acid carboxamides with iodoacetanilides and Mills azo coupling.

Optical, electrochemical and photocatalytic properties of cobalt doped CsPbCl3 nanostructures: a one-pot synthesis approach.

The present manuscript aims at the synthesis of cesium based halide perovskite nanostructures and the effect of cobalt doping on the structural, optical, lumnisent, charge storage and photocatalytic properties. In a very first attempt, we report the solvothermal synthesis of Co doped CsPbCl3 nanostructures under subcritical conditions. The structural features were demonstrated by X-ray diffraction (XRD) Surface morphology determined cubic shape of the synthesized particles. Doping is an excellent way to modify the properties of host material in particular to the electronic structure or optical properties. Incorporation of Co2+ ions in the perovskite structure tunes the optical properties of the nanostructures making this perovskite a visible light active material (Eg = 1.6 eV). This modification in the optical behaviour is the result of size effect, the crystallite size of the doped nanostructures increases with cobalt doping concentration. Photolumniscance (PL) study indicated that CsPbCl3 exhibited Blue emission. Thermogravametric analysis (TGA) revealed that the nanostructures are quite stable at elavated temperatures. The electrochemical performance depicts the pseudocapacative nature of the synthesized nanostructures and can used for charge storage devices. The charge storage capability showed direct proportionality with cobalt ion concentration. And Finally the photocatalytic performance of synthesized material shows superior catalytic ability degrading 90% of methylene blue (MB) dye in 180 min under visible light conditions.

Facile Way of Making Hydrothermally Synthesized Crystalline SrSnO3 Perovskite Nanorods Suitable for Blue LEDs and Spintronic Applications.

Mn doping in SrSnO3 perovskite material via hydrothermal process under subcritical conditions is reported for the very first time. The present article aims to carry this perovskite suitable for blue light-emitting diodes (LEDs) and spintronic applications. The influence of various Mn doping percentages on structural, morphological, compositional, optical, photoluminescent, and magnetic properties of SrSnO3 is demonstrated. The perovskite material is grown in an orthorhombic crystal structure having a space symmetry of Pnma along with point group of mmm as determined from the Rietveld refinement. Doping is an excellent way to modify the properties of wide-band-gap perovskite nanostructures. Incorporation of Mn is the result of exact substitution. Morphological studies indicate formation of rodlike structures with thickness in nanoscale dimensions (180-280 nm), and the thickness is a function of doping concentration. The higher doping concentration resulted in enhanced growth of the nanorods. Selected area electron diffraction (SAED) results showed the single-crystal nature of the nanorods. Thermogravimetric analysis (TGA) confirmed the high stability of the material at elevated temperatures. Also, the doped perovskite material is transparent in the visible light, active in the ultraviolet region having a band gap of ∼2.78 eV, and is tuned up to 2.25 eV as the Mn doping concentration reaches 10%. The transfer of excitonic energy from the host material to the dopant Mn2+ ion leads to the formation of spin-forbidden [4T1-6A1] emission. Later on, photoluminescence study indicates an enhancement in luminescence behavior of Mn doped perovskite nanostructures. The Commission Internationale de l'éclairage (CIE) diagram drawn to find the color coordinates of the nanorods determines their suitability for blue LEDs. In addition, Mn doping results the conversion of diamagnetic SrSnO3 into a ferromagnetic material, making the nanorods suitable for spintronic applications.

Growth and properties of hydrothermally derived crystalline ZnSe quantum dots.

Chalcogenide nanostructures are the materials with diverse applications. Here, we report rapid hydrothermal synthesis of crystalline ZnSe quantum dots (QDs), avoiding the use of toxic chemicals. To the best of our knowledge, this is the first report on very rapid (5 h) hydrothermal synthesis of pristine ZnSe QDs. Elemental selenium is used as a source for selenium. Structural, morphological, compositional, and optical properties of the semiconductor were studied. Structural properties (X-ray diffraction) demonstrate that the particles have grown in a single cubic phase. Morphological studies show formation of agglomerated QDs (4 nm). The material possess stoichiometric ratio of the constituent elements that are uniformly distributed. Selected area electron diffraction (SAED) study indicated the material is polycrystalline in nature. Optical properties demonstrated that the QDs are suitable for optoelectronic devices exhibiting room temperature photoluminescence. Commission Internationale de l'Éclairage (CIE) chromaticity diagram shows the material exhibits violet emission and hence suitable for violet LEDs that have potential ability in clinical applications.

Medicinal and biological potential of pumpkin: an updated review.

The use of herbal remedies individually or in combination with standard medicines has been used in various medical treatises for the cure of different diseases. Pumpkin is one of the well-known edible plants and has substantial medicinal properties due to the presence of unique natural edible substances. It contains several phyto-constituents belonging to the categories of alkaloids, flavonoids, and palmitic, oleic and linoleic acids. Various important medicinal properties including anti-diabetic, antioxidant, anti-carcinogenic, anti-inflammatory and others have been well documented. The purpose of the present article is to discuss various medicinal and biological potentials of pumpkin that can impart further research developments with this plant for human health benefits.

Synthesis and surfactant modification of clinoptilolite and montmorillonite for the removal of nitrate and preparation of slow release nitrogen fertilizer.

This article introduces the synthesis of clinoptilolite and montmorillonite, and their surfactant modification by using solutions of hexadecyltrimethylammonium bromide (CH(3)(CH(2))(15)N(Br)(CH(3))(3), HDTMAB) and dioctadecyldimethylammonium bromide ((CH(3)(CH(2))(17))(2)N(Br)(CH(3))(2), DODMAB). The feasibility of using surfactant modified silicates (SMSs) as a potential adsorbent for nitrate and for slow release of nutrient has been investigated. Adsorption isotherms of NO(3)(-) on SMSs have been measured at aqueous concentration of 160-280 mg L(-1). The SMSs show much higher adsorption capacity than the unmodified materials as determined by Langmuir adsorption isotherm. The surfactant modification and increased surfactant loading concentration enhance the nitrate anion retaining capacity of silicates (montmorillonite (16.05 mg g(-1))

Sorption behaviour of nanocrystalline MOR type zeolite for Th(IV) and Eu(III) removal from aqueous waste by batch treatment.

The nanocrystalline mordenite (MOR) type zeolite materials with initial chemical composition Na(2)O:Al(2)O(3):10SiO(2):48H(2)O have been synthesized under hydrothermal conditions. MOR1 and MOR2 are spherically shaped nanocrystals, whereas MOR3 and MOR4 have rod-like morphology. This paper reports the sorption characteristics of MOR analogues for Th(IV) and Eu(III) removal from aqueous nuclear waste. Sorption of Th(IV) and Eu(III) on MOR1, MOR2, MOR3 and MOR4 in a single component system with varying initial metal ion concentration, solution pH, contact times, sorbent dose and temperatures has also been investigated. Further, the Langmuir and Freundlich sorption models have been applied to describe equilibrium isotherms at different temperatures. The adsorption capacity increases largely with increasing solution pH and temperature of the system. Specific surface area and pore volume have been investigated by Brunauer-Emmett-Teller (BET) method. The N(2) adsorption isotherm presents a type IV isotherm with narrow hysteresis loop which indicates the presence of mesopores related to inter-particle voids. Thermodynamic results indicate that the sorption follows an endothermic physisorption process. It has been found that these exchangers have good sorption capacity and out of which MOR4 has highest sorption capacity. Thus, nanocrystalline MOR4 is proved to be good sorbent for both Th(IV) and Eu(III).

Complementary and comparative study on hypoglycemic and antihyperglycemic activity of various extracts of Eugenia jambolana seed, Momordica charantia fruits, Gymnema sylvestre, and Trigonella foenum graecum seeds in rats.

In present study, we investigated hypoglycemic and antihyperglycemic potential of five extracts (water, ethanol, methanol, hexane, and chloroform) of four plants (i.e., seeds of Eugenia jambolana, fruits of Momordica charantia, leaves of Gymnema sylvestre, and seeds of Trigonella foenum graecum) alone and/or in combination with glimepiride in rats. Ethanol extract of E. jambolana, water extract of M. charantia, ethanol extract of G. sylvestre, and water extract of T. graecum exhibited highest hypoglycemic and antihyperglycemic activity (most active) in rats among all the extracts, while hexane extracts exhibited least activities. Most active extracts were further studied to dose-dependent (200, 100, and 50 mg/kg body weight (bw)) hypoglycemic and antihyperglycemic effects alone and in combination with glimepiride (20, 10, and 5 mg/kg bw). The combination of most active extracts (200 mg/kg bw) and lower dose of glimepiride (5 mg/kg bw) showed safer and potent hypoglycemic as well as antihyperglycemic activities without creating severe hypoglycemia in normal rats, while higher doses (200 mg/kg bw of most active extracts, and 10 and 20 mg/kg bw of glimepiride) were generated lethal hypoglycemia in normal rats. From this study, it may be concluded that the ethanol extract of E. jambolana seeds, water extract of M. charantia fruits, ethanol extract of G. sylvestre leaves, and water extract of T. graecum seeds have higher hypoglycemic and antihyperglycemic potential and may use as complementary medicine to treat the diabetic population by significantly reducing dose of standard drugs.

Sorption of 137Cs, 133Ba and 154Eu by synthesized sodium aluminosilicate (Na-AS).

Sodium aluminosilicate has been synthesized by solution route for use as a sorbent for various radionuclides. It was characterized by XRD, zeta potential, BET surface area, FTIR spectroscopy and site density measurement. Sorption studies of (137)Cs, (133)Ba and (154)Eu on synthesized sodium aluminosilicate have been carried out at varying pH (3-10). Sorption of all the metal ions was found to increase with pH of suspension with the saturation value increasing with the oxidation state of metal ion. Effect of Aldrich humic acid (2mg/l) on sorption was also investigated. In case of (137)Cs, the sorption was not affected by the presence of humic acid, while in case of (133)Ba and (154)Eu, sorption was enhanced at lower pH and decreased at higher pH in presence of HA. A series of experiments were carried out for (154)Eu sorption on sodium aluminosilicate at various conditions. Sorption of europium was analyzed by different sorption isotherms, viz., Freundlich and D-R isotherm. Thermodynamic data reveal sorption phenomena as endothermic and spontaneous. Studies were further extended to find out effect of diverse ions (Ca(2+) and CO(3)(2-)) on sorption of europium.

Synthesis and characterization of an analogue of heulandite: sorption applications for thorium(IV), europium(III), samarium(II) and iron(III) recovery from aqueous waste.

The synthesis of needle/fibrous particles of analogue of heulandite with particle diameter of 0.08 microm, length 4-8 microm and high specific surface area (478 m(2) g(-1)) with cation exchange capacity (3.27 mequiv g(-1)) have been achieved. The heulandite needles were obtained by using inorganic salts as a source for silicon and aluminum in the hydrothermal synthesis of the material. Alkalinity of the medium played an important role in the formation of heulandite fibers, as it affects the nucleation rate of zeolite synthesis. The analogue of heulandite was characterized using spectroscopic, thermal analysis, scanning and adsorption techniques. After mechanical grinding of crystals of heulandite, obtained powder was used for the study of radionuclide recovery from aqueous waste. The adsorption experiments were carried out under batch process with, pH of medium, amount of sorbent, time of contact between sorbate and sorbent, metal ion concentration and temperature as the variables. The adsorption was strongly dependent on pH of the medium and the uptake of all the metal ions increased from pH 1.0 to 9.0 and the maximum sorption was noticed in the pH range of 5.0-7.0. The optimum condition for these metal ions (Th(IV), Eu(III), Sm(II), and Fe(III)) sorption on self synthesized analogue of heulandite was; 0.001 N metal ion concentration, equilibration time of 4 h, 100 mg sorbent dose and 313-323 K temperature. This sorption process is fit to both Langmuir and Freundlich sorption isotherm. Thermodynamic studies predict the endothermic and spontaneous nature of the same.

Role of magnetite and humic acid in radionuclide migration in the environment.

Sorption of (137)Cs, (90)Sr, (154)Eu and (141)Ce by magnetite has been studied at varying pH (4 to 11) in the presence and absence of humic acid. The sorption studies have also been carried out at varying ionic strength (0.01 to 0.2 M NaClO(4)) and humic acid concentration (2 to 20 mg/L). Percentage sorption of (137)Cs and (90)Sr was found to be pH dependent, with the sorption increasing with increasing pH of the suspension. At any pH, the percentage sorption of (90)Sr was higher than that of (137)Cs. The results have been explained in terms of the electrostatic interaction between the positively charged metal ions and the surface charge of the magnetite which becomes increasingly negative with increasing pH. On the other hand, (154)Eu and (141)Ce were found to be strongly sorbed by the magnetite at all pH values, with the sorption being independent of pH. The strong sorption of trivalent and tetravalent metal ions suggests the role of complexation reactions during sorption, apart from the electrostatic interactions. However, in the case of (141)Ce surface precipitation of Ce(III) formed by reduction of Ce(IV) in the presence of magnetite cannot be ruled out. Presence of humic acid (2 mg/L) was found to have negligible effect on sorption of all metal ions.

Biological and medicinal properties of grapes and their bioactive constituents: an update.

The grape is one of the most valued conventional fruits, worldwide. Although most of the parts of the grapevine are useful, primarily, the grape is considered as a source of unique natural products not only for the development of valuable medicines against a number of diseases, but also for manufacturing various industrial products. Over the last few decades, apart from the chemistry of grape compounds, considerable progress has been made towards exploring the biological activities of various grape-derived constituents. Today, it is well established that in addition to serving as food, the grape is a major source of several phytochemicals. The main biologically active and well-characterized constituent from the grape is resveratrol, which is known for various medicinal properties in human diseases. This review discusses the roles of various grape-derived phytochemicals in relation to various diseases.

Synthesis and morphological studies of nanocrystalline MOR type zeolite material.

A number of nanosize mordenite (MOR) analogues with particle size ranging from 5 to 50 nm were synthesized by the hydrothermal method. The effect of various growth parameters like: alkalinity of the medium, type of silica source, etc. on crystal morphology and the crystal size of MOR type of zeolites was investigated. Specific surface and micropore volume were investigated by the Brunauer-Emmett-Teller (BET) method. XRD, SEM, TEM studies indicate nanosize growth of the MOR type crystals. Electron diffraction patterns confirm the crystalline nature of the nanoparticles and the results of their indexing prove that the material is MOR. These synthesized materials show microporous as well mesoporous character. In the case of MOR material synthesized using sodium silicate, it was found that an increase in the alkalinity of the medium led to changes in the morphology and crystal size of the material. For low concentrations of NaOH, the crystallites were spherical in shape whereas at high concentrations, they were in the shape of nanorods of diameter 25 to 50 nm. The morphology of the MOR material synthesized using tetraethyl orthosilicate (TEOS), on the other hand, did not change when the NaOH concentration was increased beyond 2.0 molar.

Studies on the sorption of As(III) on the synthetic gel sodium potassium fluorophlogopite.

Sorption of As(III) has been studied on the synthesized gel close to Sodium potassium fluorophlogopite [Na0.5K0.5Mg3 (Si3 AlO10) F2] as a function of initial solution concentration at pH 2,4 and 7. The effect of parameters like equilibration time (0.5 - 24.0 hr), weight of the exchanger (30-150 mg) and temperature (25 degrees - 45 degrees c) has been investigated. The uptake of metal ion, As(III) has been expressed in terms of distribution coefficient i.e. (kd) values.