Effective PET and ICT switching of boradiazaindacene emission: a unimolecular, emission-mode, molecular half-subtractor with reconfigurable logic gates

[reaction, structure: see text] We report a unimolecular system functioning as a combinatorial logic circuit for half-subtractor. The emission characteristics can be modulated by chemical inputs, and when followed at two different wavelengths, two functionally integrated logic gates XOR and INHIBIT are obtained. Both logic gates function in the emission mode, and with very large differences in the signal intensity allowing unequivocal assignment of logic-0 and logic-1.     

Ion sensing coupled to resonance energy transfer: a highly selective and sensitive ratiometric fluorescent chemosensor for Ag(I) by a modular approach

We report a novel dimeric boradiazaindacene dye which can be converted in one step to an efficient resonance energy transfer (RET) dyad. In addition, if this modification is done with appropriate ligands, RET can be coupled to ion sensing. The utility of this approach is demonstrated in a highly selective, emission ratiometric chemosensor for Ag(I).     

Synthesis of some 6,8‐diarylimidazo[1,2‐a]pyrazine derivatives by using either reflux or microwave irradiation method and investigation of their anticancer activities

In order to obtain some 6,8‐diarylimidazo[1,2‐a]pyrazines, 1‐(2‐aryl‐2‐oxoethyl)‐2‐aryloylimidazole derivatives were reacted with ammonium acetate in acetic acid by using a new method different from that found in the literature. Anticancer activities of the compounds obtained were evaluated and the noticeable activity values were reported.     

Auto-Bäcklund transformations and solitary wave solutions for the nonlinear evolution equation

In the present work, according to the concept of extended homogeneous balance method and with help of Maple, we get auto-Bäcklund transformations for a (2 + 1)-dimensional nonlinear evolution equation. Subsequently, by using these auto-Bäcklund transformation, exact explicit solutions of this equation are obtained.     

Potassium Sensing by Using a Newly Synthesized Squaraine Dye in Sol-Gel Matrix

Squaraines are a group of fluorescent dyes and pigments derived from squaric acid and dialkylanilines well known in applications such as photoreceptors, organic solar cells, optical recording media, and non-linear optics. Their very promising spectral properties, long wavelength absorption and emission, and high absorptivity and quantum yields have not been exploited so far in relation to optical sensor design. They exhibit excellent solubility in sol-gel matrices, and the ligand is an integral part of the fluorophore system, which makes the molecule a fluoroionophore. In this work, potassium-sensing agent, bis[4-N-(1-aza-4,7,10,13,16-pentaox acyclooctadecyl)-3,5-dihydroxyphenyl] squaraine has been used for potassium sensing in a sol-gel matrix. The spectrofluorimetric response of dye-doped tetraethyl ortosilicate (TEOS) film after exposure to certain concentrations of K⁺ has been investigated, and 62% of relative signal change was achieved. The dynamic working range of the sensor membrane has been found between 10^–9 and 10^–6 M K⁺, in other terms from nanomolar to micromolar levels, which is an advantage over flame emission spectroscopy, in view of detection limit. The sensor is fully reversible within the dynamic range and the response time (₉₀) is found to be 2 min under batch conditions. The cross-sensitivity of the molecule to Na⁺, Ba²⁺, Ca²⁺, and NH⁺ ₄ was also tested in separate solutions.     

Resonant non-linear vibrations in continuous systems—I. Undamped case

A method is presented for obtaining periodic solutions to forced oscillations of non-linear systems governed by equations of the form u_ss?u_yy?εf(u,u,_y,u_yy…,s) = 0. The method is presented by application to the equation u_ss?u_yy?εu²_yu_yy= 0 which governs the vibrations of a soil layer that is free on the top surface and is forced harmonically at the bedrock. It is shown that unlike the ODE case (Duffing equation), the PDE requires an infinite number of periodicity conditions to correctly characterize the resonant region and these conditions lead to an infinite number of branches in the dispersion spectrum. Calculations indicate that these branches tend to an envelope curve. The uniform approach presented by Millmann and Keller is discussed in order to determine in what sense it can be viewed as an effective approximation for the fundamental mode.     

Fractionation and Bioaccessibility of Manganese,Copper, Zinc,Cadmium, and Lead in Commercial Vegetable and Rice Baby Foods Using Inductively Coupled Plasma - Mass Spectrometry (ICP-MS) with Central Composite Design (CCD)

Abstract

Herein the bioaccessibility of Mn, Cu, Zn, Cd, and Pb, selected from essential and toxic elements, was determined in commercially sold vegetable purees intended for infant and toddler consumption. Chemical fractionation studies using water, acetone, diethyl ether, chloroform:methanol, and n-hexane were employed to predict the importance of the protein and lipid parts of a matrix to assess the bioaccessibility data. In addition, in-vitro gastrointestinal digestion was performed to determine the bioaccessibility of the elements using a five level, three factor central composite design (CCD) to maximize the elemental solubility. The total elemental concentrations in all of the fractions were determined by inductively coupled plasma – mass spectrometry (ICP-MS). Based on the consumption of one jar of vegetable/rice-based baby food, Zn was 1.3% of the recommended dietary allowance and Mn was 4.2% of the adequate intake level, while Cu was almost 100% of the adequate intake level. Additionally, Pb was always below the detection limit and Cd was sometimes under the detection limit for the percent bioaccessibility. However, in some samples, Cd was as high as 80% of the tolerable weekly intake level depending on the body weight.     

Building an Iron Chromophore Incorporating Prussian Blue Analogue for Photoelectrochemical Water Oxidation

The replacement of traditional ruthenium-based photosensitizers with low-cost and abundant iron analogs is a key step for the advancement of scalable and sustainable dye-sensitized water splitting cells. In this proof-of-concept study, a pyridinium ligand coordinated pentacyanoferrate(II) chromophore is used to construct a cyanide-based CoFe extended bulk framework, in which the iron photosensitizer units are connected to cobalt water oxidation catalytic sites through cyanide linkers. The iron-sensitized photoanode exhibits exceptional stability for at least 5 h at pH 7 and features its photosensitizing ability with an incident photon-to-current conversion capacity up to 500 nm with nanosecond scale excited state lifetime. Ultrafast transient absorption and computational studies reveal that iron and cobalt sites mutually support each other for charge separation via short bridging cyanide groups and for injection to the semiconductor in our proof-of-concept photoelectrochemical device. The reorganization of the excited states due to the mixing of electronic states of metal-based orbitals subsequently tailor the electron transfer cascade during the photoelectrochemical process. This breakthrough in chromophore-catalyst assemblies will spark interest in dye-sensitization with robust bulk systems for photoconversion applications.     

Determination of some phthalate acid esters in artificial saliva by gas chromatography-mass spectrometry after activated carbon enrichment

The determination of six phthalate acid esters was achieved in artificial saliva using gas chromatography-mass spectrometry following activated carbon enrichment of samples. Central composite experimental design was applied to optimize method parameters, such as pH, adsorption time and amount of activated carbon. The best compromise of analytical conditions for the simultaneous determination of analytes from spiked artificial saliva were found to be: pH (3), adsorption time (30 min), activated carbon amount (1.8 g L⁻¹) and elution solvent (chloroform). These conditions were applied to study the migration of phthalate acid esters from different children's toys into saliva. A horizontal agitation method was applied to extract the analytes from plastic toys into saliva for 2 h at 37 °C. The detection limits of the method were in the range of 1.3-5.1 μg L⁻¹, while the relative standard deviation (%) values for the analysis of 100 μg L⁻¹ of the analytes were below 3.0% (n = 5). Di-2-ethylhexyl phthalate was the main analyte found in these samples.     

Nafion-graphene composite film modified glassy carbon electrode for voltammetric determination of p-aminophenol

A Nafion-graphene (Nafion-GR) nanocomposite film modified glassy carbon electrode was fabricated by a simple drop-casting method, and used in the electrochemical detection of p-aminophenol (4-AP). Owing to the large surface area, good conductivity of GR and good affinity of Nafion, the sensor exhibited excellent electrocatalytic activity for the oxidation of 4-AP. The electrochemical behaviors of 4-AP on Nafion/GR film modified glassy carbon electrodes were investigated by cyclic voltammetry and differential pulse voltammetry. A calibration curve is constructed in the same matrix, urine, as the unknown samples to be analyzed. The Nafion-GR film modified electrode was linearly dependent on the 4-AP concentration and the linear analytical curve was obtained in the ranges of 0.5–200 μM with differential pulse voltammetry (DPV) and the detection limit was 0.051 μM. The Nafion-graphene nanocomposite modified electrode exhibited good reusability than pure graphene modified GCE. This procedure can be used for the determination of p-aminophenol in the presence of its degradation products and paracetamol. Finally, the proposed method was successfully used to determine p-aminophenol in local tap water samples in urine samples and pharmaceutical preparations.