(Acetato‐κO)[tris(3,5‐dimethylpyrazol‐1‐yl‐κN2)hydroborato]zinc(II)

The title complex, [Zn(C₁₅H₂₂BN₆)(C₂H₃O₂)] or (Tp^Me,Me)Zn(OAc), contains a tripodal tris(pyrazolyl)hydroborate ligand, a monodentate acetate ligand and a Zn^II centre in a distorted tetrahedral coordination environment capped on one triangular face by a secondary Zn...O interaction with the second O atom of the acetate ligand. The four‐coordination of Zn^II and the essentially monodentate character of the acetate ligand are due to the high steric demands of the ligand set, which prevent chelate formation and five‐coordination and lead to relatively long Zn—O and Zn—N bonds compared with related complexes of Zn^II and other metals.     

Binding of cetylpyridinum chloride to glucose oxidase

The binding of cetylpyridinum chloride (CPC) with glucose oxidase (GOD) has been extensively studied at various experimental conditions such as ionic strength, urea concentration and pH at 25 °C, using ion-selective membrane electrodes, UV–vis absorption spectroscopy and enzyme activity assay method. The accurate binding isotherms have been obtained and analyzed in terms of Scatchard plot and binding capacity concept. The results represent two binding set system for most of studied conditions. The values of Hill equation parameters have been estimated and used for calculation of intrinsic Gibbs free energy of binding. The results have been interpreted in terms of structural viewpoint of GOD and nature of interactions in the solution. The interpretations are in good agreement with denaturation experiment. Activity measurements represent the significant activation of enzyme due to binding of first CPC molecules. However, the binding of subsequent CPC diminished the activity of enzyme which may be due to the binding of second CPC to enzyme active site. The complete deactivation of enzyme is reached due to binding of about five CPC ions.     

Synthesis of salicylaldehyde-modified mesoporous silica and its application as a new sorbent for separation, preconcentration and determination of uranium by inductively coupled plasma atomic emission spectrometry

A new functionalized mesoporous silica (MCM-41) using salicylaldehyde was utilized for the separation, preconcentration and determination of uranium in natural water by inductively coupled plasma atomic emission spectrometry (ICP-AES).Experimental conditions for effective adsorption of trace levels of U(VI) were optimized. The preconcentration factor was 100 (1.0 mL of elution for a 100 mL sample volume). The analytical curve was linear in the range 2-1000 μg L⁻¹ and the detection limit was 0.5 ng mL⁻¹. The relative standard deviation (R.S.D.) under optimum conditions was 2.5% (n = 10). Common coexisting ions did not interfere with the separation and determination of uranium at pH 5. The sorbent exhibited excellent stability and its sorption capacity under optimum conditions has been found to be 10 mg of uranium per gram of sorbent. The method was applied for the recovery and determination of uranium in different water samples.     

Inhibitory effects of Ruta graveolens L. extract on guinea pig liver aldehyde oxidase

Ruta graveolens L. is a flavonoid-containing medicinal plant with various biological properties. In the present study, the effects of R. graveolens extract on aldehyde oxidase, a molybdenum hydroxylase, are investigated. Aldehyde oxidase was partially purified from liver homogenates of mature male guinea pigs by heat treatment and ammonium sulphate precipitation. The total extract was obtained by macerating the aerial parts of R. graveolens in MeOH 70% and the effect of this extract on the enzyme activity was assayed using phenanthridine, vanillin and benzaldehyde as substrates. Quercetin and its glycoside form, rutin were isolated, purified and identified from the extract and their inhibitory effects on the enzyme were investigated. R. graveolens extract exhibited a high inhibition on aldehyde oxidase activity (89-96%) at 100 microg/ml which was comparable with 10 microM of menadione, a specific potent inhibitor of aldehyde oxidase. The IC50 values for the inhibitory effect of extract against the oxidation of benzaldehyde, vanillin and phenanthridine were 10.4, 10.1, 43.2 microg/ml, respectively. Both quercetin and rutin at 10 microM caused 70-96% and 27-52% inhibition on the enzyme activity, respectively. Quercetin was more potent inhibitor than rutin, but both flavonols exerted their inhibitory effects mostly in a linear mixed-type.     

A free-energy landscape picture and Landau theory for the dynamics of disordered materials

Landau's theory of phase transitions [Nature (London) 138, 840 (1936); Statistical Physics (Pergamon, London, 1959)] is adapted to treat independently relaxing regions in complex systems using nanothermodynamics. The order parameter we use governs the thermal fluctuations, not a specific static structure. We find that the entropy term dominates the thermal behavior, as is reasonable for disordered systems. Consequently, the thermal equilibrium occurs at the internal-energy maximum, so that the potential-energy minima have negligible influence on the dynamics. The dynamics involves normal thermal fluctuations about the free-energy minimum, with a time scale that is governed by the curvature of the internal-energy maximum. The temperature dependence of the fluctuations yields Vogel-Tamman-Fulcher-type [Phys. Z. 22, 645 (1921); J. Am. Ceram. Soc. 8, 339 (1925); Z. Anorg. Allg. Chem. 156, 245 (1926)] relaxation rates and approximate time-temperature superposition, consistent with the Williams-Landell-Ferry [J. Am. Chem. Soc. 77, 3701 (1955)] procedure for analyzing the dynamics of complex fluids, while the size dependence of the fluctuations provides an explanation for the distribution of relaxation times and heterogeneity that are found in glass-forming liquids, thus providing a unified picture for several features in the dynamics of disordered materials.     

Flow injection chemiluminescence analysis of phenolic compounds using the NCS-luminol system

A flow injection system coupled with two simple and sensitive chemiluminescence (CL) methods is described for the determination of some phenolic compounds. The methods are based on the inhibition effects of the investigated phenols on the CL signal intensities of N-chlorosuccinimide-KI-luminol (NCS-KI-luminol) and NCS-luminol systems. The influences of the chemical and hydrodynamic parameters on the decrease in CL signal intensities of NCS-KI-luminol and NCS-luminol systems for hydroquinone, catechol, and resorcinol, serving as the model compounds of analyte, were studied in the flow injection mode of analysis. Under the selected conditions, the proposed CL systems were used for the determination of some phenolic compound and analytical characteristics of the systems including calibration equation, correlation coefficient, linear dynamic range, limit of detection, and sample throughput. The limits of detection for hydroquinone, catechol, and resorcinol were 0.002, 0.01, and 0.3 μM using the NCS-KI-luminol system; for the NCS-luminol system these were 0.01, 0.17, and 1.6 μM, respectively. The relative standard deviation for 10 repeated measurements of 0.04, 0.06, and 1 μM of hydroquinone, catechol, and resorcinol were 1.9, 1.4, and 2.0%, respectively, with the NCS-KI-luminol system; for 0.2, 0.5, and 4 μM of hydroquinone, catechol, and resorcinol these were 2.6, 2.2, and 3.7%, respectively, using the NCS-luminol system. The method was applied to the determination of catechol in known environmental water samples with a relative error of less than 6%. A possible reaction mechanism of the proposed CL system is discussed briefly.      

Some properties of autocentral automorphisms of a group

Let G be a group, Aut(G) and L(G) denote the full automorphisms group and absolute centre of G, respectively. The automorphism \({\alpha\in Aut(G)}\) is called autocentral if \({g^{-1}\alpha(g)\in L(G)}\), for all \({g\in G}\). In the present paper, we investigate the properties of such automorphisms.     

Solving an inverse problem for a generalized time-delayed Burgers-Fisher equation by Haar wavelet method

In this paper, a numerical method consists of combining Haar wavelet method and Tikhonov regularization method to determine unknown boundary condition and unknown nonlinear source term for the generalized time-delayed Burgers-Fisher equation using noisy data is presented. A stable numerical solution is determined for the problem. We also show that the rate of convergence of the method is as exponential $\Bigl(O\left(\frac{1}{2^{J+1}}\right)\Bigr)$, where $J$ is maximal level of resolution of wavelet. Some numerical results are reported to show the efficiency and robustness of the proposed approach for solving the inverse problems.     

Around Jensen’s inequality for strongly convex functions

In this paper we use basic properties of strongly convex functions to obtain new inequalities including Jensen type and Jensen–Mercer type inequalities. Applications for special means are pointed out as well. We also give a Jensen’s operator inequality for strongly convex functions. As a corollary, we improve the Hölder-McCarthy inequality under suitable conditions. More precisely we show that if \(Sp\left( A \right) \subset \left( 1,\infty \right) \), then

$$\begin{aligned} {{\left\langle Ax,x \right\rangle }^{r}}\le \left\langle {{A}^{r}}x,x \right\rangle -\frac{{{r}^{2}}-r}{2}\left( \left\langle {{A}^{2}}x,x \right\rangle -{{\left\langle Ax,x \right\rangle }^{2}} \right) ,\quad r\ge 2 \end{aligned}$$

and if \(Sp\left( A \right) \subset \left( 0,1 \right) \), then

$$\begin{aligned} \left\langle {{A}^{r}}x,x \right\rangle \le {{\left\langle Ax,x \right\rangle }^{r}}+\frac{r-{{r}^{2}}}{2}\left( {{\left\langle Ax,x \right\rangle }^{2}}-\left\langle {{A}^{2}}x,x \right\rangle \right) ,\quad 0<r<1 \end{aligned}$$

for each positive operator A and \(x\in \mathcal {H}\) with \(\left\| x \right\| =1\).