Boron nitride nanocluster as a carrier for lomustine anticancer drug delivery: DFT and thermodynamics studies

Monatshefte für Chemie - Chemical Monthly - Previous reports were shown that boron nitride nanostructures can be biocompatible and nontoxic. Therefore, interaction of lomustine as an...     

Visible light-induced degradation of phenolic compounds by Sudan black dye sensitized TiO2 nanoparticles as an advanced photocatalytic material

Research on Chemical Intermediates - Using a simple impregnation process, the present study has introduced a novel route for the photosensitization of TiO2 nanoparticles using Sudan black B dye as...     

Tucker core consistency for validation of restricted Tucker3 models

In Tucker3 analysis of three-way data array obtained from a chemical or biological system, it is sometimes possible to use a priori knowledge about the system to specify what is called a restricted Tucker3 model. Often, the restricted Tucker3 model is characterized by having some elements of the core forced to zero. As a simple example, an F-component PARAFAC model can be seen as a restricted (F, F, F) Tucker3 model in which only superdiagonal elements of the core are allowed to be nonzero. The core consistency diagnostic was previously introduced by Bro and Kiers for determining the proper number of components in PARAFAC analysis. In the current study, this diagnostic is extended to other restricted Tucker3 models to validate the appropriateness of the applied constraints. The new diagnostic is named Tucker core consistency (TuckCorCon). When the dimensionality and the pattern of the restricted core is valid, the simple core of restricted Tucker3 model and a corresponding unrestricted core will be similar and in this case the TuckCorCon will be close to maximum (100%). A simulated chemical equilibrium data set and two experimental data sets were used to evaluate the applicability of the TuckCorCon to decide about the appropriateness of dimensionality and pattern of the core nonzero elements in the restricted Tucker3 models.     

Ugi reaction of thiouridocarboxylic acids: A synthesis of thiourea-peptoids

Benzoylthioureidocarboxylic acids, prepared from benzoyl chlorides, potassium thiocyanate, and α-aminoacids, are used as acid components in the Ugi reaction to produce thiourea-peptoids in moderate to good yields.     

Advances,opportunities, and challenges of hydrogen and oxygen production from seawater electrolysis: An electrocatalysis perspective

With increasing energy consumption and greenhouse gas emissions, the importance of developing renewable energy sources to replace fossil fuels has become a vital global task. Hydrogen produced via water electrolysis powered by renewable energy systems at a large scale is an essential measure to reduce greenhouse gas and particulate emissions. Electrolysers use a substantial amount of water (mainly freshwater) to produce hydrogen and oxygen at the cathode, and anode, respectively. However, seawater is preferred because it is the most abundant water resource. Although many R&D efforts on seawater electrolysis have been carried out since the 1970s, the barriers are the undesired chlorine gas evolution reaction at the anode, and corrosion induced by chloride ions. Unlike the available data for electrocatalyst materials based upon platinum group metals in pure solutions, limited data is available for electrocatalysts in seawater. Therefore, there is an urgent need to develop new electrocatalysts for seawater electrolysis.     

The anticancer impacts of N,S donor pyrazole based ligand and its Co(III) and Cu(II) complexes on breast cancer cells

Transition Metal Chemistry - The development of suitable compounds for the effective treatment of cancer is highly demanded. Inorganic complexes based on cobalt and copper centers have revealed a...     

Determination of cobalt in water samples by atomic absorption spectrometry after pre-concentration with a simple ionic liquid-based dispersive liquid-liquid micro-extraction methodology

A rapid dispersive liquid-liquid micro-extraction (DLLME) methodology based on the application of 1-hexylpyridinium hexafluorophosphate [C₆py][PF₆] ionic liquid (IL) as an extractant solvent was applied for the pre-concentration of trace levels of cobalt prior to determination by flame atomic absorption spectrometry (FAAS). 1-Phenyl-3-methyl-4-benzoyl-5-pyrazolone (PMBP) was employed as a chelator forming a Co-PMBP complex to extract cobalt ions from aqueous solution into the fine droplets of [C₆py][PF₆]. Some effective factors that influence the micro-extraction efficiency include the pH, the PMBP concentration, the amount of ionic liquid, the ionic strength, the temperature and the centrifugation time which were investigated and optimized. In the optimum experimental conditions, the limit of detection (3s) and the enrichment factor were 0.70 μg L⁻¹ and 60, respectively. The relative standard deviation (RSD) for six replicate determinations of 50 μg L⁻¹ Co was 2.36%. The calibration graph using the pre-concentration system was linear at levels 2–166 μg L⁻¹ with a correlation coefficient of 0.9982. The applicability of the proposed method was evaluated by the determination of trace amounts of cobalt in several water samples.