Flux synthesis of the noncentrosymmetric cluster compounds Cs2SnAs2Q9 (Q = S,Se) containing two different polychalcoarsenite beta-[AsQ4]3- and [AsQ5]3- ligands

Two noncentrosymmetric quaternary tin chalcoarsenates, Cs(2)SnAs(2)S(9) (1) and Cs(2)SnAs(2)Se(9) (2), were synthesized by the polychalcoarsenate flux method. Compound 1 crystallizes in the orthorhombic space group Pmc2(1) with a = 7.386(3) A, b = 14.614(5) A, c = 14.417(5) A, and Z = 4. Compound 2 crystallizes in the monoclinic space group P2(1) with a = 7.715(5) A, b = 17.56(1) A, c = 7.663(5) A, beta = 115.86(1) degrees, and Z = 2. Both structures contain the same tin-centered molecular cluster anions [Sn[AsQ(2)(Q(2))][AsQ(Q(2))(2)]](2)(-) (Q = S, Se) separated by Cs cations. The Sn(4+) ion is in a distorted octahedral environment coordinated by two different pyramidal-shaped tridentate ligands, [AsQ(2)(Q(2))](3)(-) and [AsQ(Q(2))(2)](3)(-). These compounds absorb visible light at energies above 1.98 and 1.45 eV for 1 and 2, respectively. Differential thermal analysis revealed that 1 melts at 350 degrees C and on cooling gives a glass. The glass recrystallizes at 268 degrees C upon subsequent heating. Compound 2 melts at 258 degrees C.     

Spectrophotometric method for the determination of demeclocycline using sodium molybdate as analytical reagent

By means of spectroscopic methods it has been found that demeclocycline reacts with molybdate ions forming a complex compound [MoO₃HDMTC]^2–. The relative stability constant of this compound has been determined by applying spectrophotometric methods. Under optimum conditions for complex formation a very sensitive spectrophotometric method for the estimation of demeclocycline in the concentration range 5.0–35.1 g/ml is proposed. The detection limit of the method is 2.5 g/ml of demeclocycline. The relative standard deviation (n=10) varies between 0.76% and 1.46%. The method proved to be accurate and sensitive for the analysis of the demeclocycline content in tablets.     

Die Sechseck-n-Waben in der Ebene,welche von n Kreisbüscheln erzeugt werden

In this paper, the problem of determining the pencils of circles which form a hexagonal n-web in E₂, is completely solved. It is well-known that n pencils of circles orthogonal to a fixed circle form a hexagonal n-web. Therefore, the main problem is the determination of all circle pencils which form a hexagonal n-web and which do not cut a fixed circle orthogonally. In this connection the following results have been obtained: The number of hexagonal 4-webs is six, whereas the number of hexagonal 5-webs is two.Finally, after having proved that the number of hexagonal 6-webs is one, it is shown that, for n7, there exist no circle pencils forming a hexagonal n-web without being orthogonal to a fixed circle.     

光纤松耦合型传感器特性研究

本文介绍一种实用的光纤传感器,它由二根光纤或多根光纤紧靠一起,并在同一位置除去局部包层,成为松耦合状态,在这种状态下,研究了它的特性和应用。 当耦合间隙中充满某种液体介质时,耦合效率明显增大,因此可以方便地判别该介质是否存在。并且实验证明了一种光纤只能有一种相近于光纤芯子折射率的介质具有最大的灵敏度。当间隙内的介质不变时,耦合功率的大小决定于耦合距离d和耦合长度l,l一旦决定以后,d的调节精度为0.1mm量级,易于在机械结构上实现线性检测。     

4,6-Thioanhydro-hexopyranosides,synthesis and chemical behaviour of methyl 2-0-p-toluenesulfonyl-4,6-thioanhydro-α-d-gulopyranoside

Methyl 4-0-benzoyl-6-bromo-6-deoxy-α-D-glucopyranoside ($\text{1}$, Figure 1) was converted, via the corresponding ditosylate $\text{2}$, into methyl 2,3-di-0-p-toluenesulfonyl-4-0-benzoyl-6-S-acetyl-6-thio-α-D-glucopyranoside ($\text{3}$) by a selective nucleophilic displacement of 6-bromo-group with thioacetate. Unexpectedly, on treating the compound $\text{3}$ with an excess of sodium methoxide in benzene-methanol (1:1) at room temperature, methyl 2-0-p-toluenesulfonyl-4,6-thioanhydro-α-D-gulopyranoside ($\text{4}$) was obtained in a yield of 84%. In order to determine the structure of the relatively unstable oily product $\text{4}$, some stable crystalline derivatives ($\text{5}$, $\text{6}$ and $\text{7}$) were prepared. Detailed analysis of the ¹H-NMR-spectra (200 MHz) of $\text{6}$ and $\text{7}$ gave the conclusive evidence for the structure of $\text{4}$ A self-imposing mechanism of the clean and smooth transformation of $\text{3}$ to $\text{4}$ is proposed, involving: a) formation of $\text{9}$ (Figure 2) as a crucial intermediate and b) a highly regioselective epoxide opening in $\text{9}$ (at C-4) by an intramolecular nucleophilic attack of the mercaptide anion from C-6.     

Electron spin resonance studies of the radiolysis of bi-π-cyclopentadienylalkyls of molybdenum and tungsten

Exposure of (C₅H₅)₂MO(CH₃)₂ and (C₅H₅)₂W(CH₃)₂, prepared from the corresponding dichlorides, to ²⁰Co γ-rays at 77 K gave H₂C.CML₃ carbene species characterised by their ESR spectra, together with a central feature possibly due to the parent cations. Dilute solutions in CD₃OD gave features assigned to the parent anions which were converted on bleaching with visible light into methyl radicals, and H₂C.ML₃ radicals. From the magnitude of the ¹H and ¹⁸³W hyperfine coupling constants, it is deduced that the SOMO for H₂C.WL₃ radicals is strongly localised on carbon.Dilute solutions in aqueous sulphuric acid also gave species with A(2H) = 20 G, identified as the carbene derivatives, H₂C.Ml₃. These were formed on annealing, as signals assigned to HSO₄ · radicals were lost.     

α-CGRP disrupts amylin fibrillization and regulates insulin secretion: implications on diabetes and migraine

Despite being relatively benign and not an indicative signature of toxicity, fibril formation and fibrillar structures continue to be key factors in assessing the structure–function relationship in protein aggregation diseases. The inability to capture molecular cross-talk among key players at the tissue level before fibril formation greatly accounts for the missing link toward the development of an efficacious therapeutic intervention for Type II diabetes mellitus (T2DM). We show that human α-calcitonin gene-related peptide (α-CGRP) remodeled amylin fibrillization. Furthermore, while CGRP and/or amylin monomers reduce the secretion of both mouse Ins1 and Ins2 proteins, CGRP oligomers have a reverse effect on Ins1. Genetically reduced Ins2, the orthologous version of human insulin, has been shown to enhance insulin sensitivity and extend the life-span in old female mice. Beyond the mechanistic insights, our data suggest that CGRP regulates insulin secretion and lowers the risk of T2DM. Our result rationalizes how migraine might be protective against T2DM. We envision the new paradigm of CGRP : amylin interactions as a pivotal aspect for T2DM diagnostics and therapeutics. Maintaining a low level of amylin while increasing the level of CGRP could become a viable approach toward T2DM prevention and treatment.

CGRP concentration is elevated in migraine conditions. The protective effect of migraine against type 2 diabetes is attributed to the ability of CGRP to remodel human amylin aggregation and to suppress the secretion of mouse insulin 2 (the orthologue of human insulin).     

Diffusion-controlled reaction. V. Effect of concentration-dependent diffusion coefficient on reaction rate in graft polymerization

The effect of diffusion on radiation-initiated graft polymerization has been studied with emphasis on the single- and two-penetrant cases. When the physical properties of the penetrants are similar, the two-penetrant problem can be reduced to the single-penetrant problem by redefining the characteristic parameters of the system. The diffusion-free graft polymerization rate is assumed to be proportional to the v power of the monomer concentration C, in which the proportionality constant a = k_pR/k, where k_p and k_t are the propagation and termination rate constants, respectively, and R_i is the initiation rate. The values of v, w, and z depend on the particular reaction system. The results of our earlier work were generalized by allowing a non-Fickian diffusion rate, obtained from an extension of the Fujita free-volume theory, which predicts an essentially exponential dependence on the monomer concentration of the diffusion coefficient, D = D₀ [exp(δC/M)], where M is the saturation concentration. It was shown that a reaction system is characterized by the three dimensionless parameters v, δ, and A = (L/2)[aM^(v?1)/D₀]^1/2, where L is the polymer film thickness. Graft polymerization tends to become diffusion controlled as A increases. Larger values of δ and v cause a reaction system to behave closer to the diffusion-free regime. The transition from diffusion-free to diffusion-controlled reaction involves changes in the dependence of the reaction rate on film thickness, initiation rate, and monomer concentration. Although the diffusion-free rate is w order in initiation rate, v order in monomer, and independent of film thickness, the diffusion-controlled rate is w/2 order in initiator rate and inverse first-order in film thickness. The dependence of the diffusion-controlled rate on monomer is dependent in a complex manner on the diffusional characteristics of the reaction system.     

Computer-assisted optimization of selectivity by tuning temperature and carrier gas pressure drop in two GC capillary columns coupled in series

The paper shows a computer-assisted procedure for the optimization of selectivity of two columns coupled in series by tuning the working temperature (using the isothermal mode) and columns coupling-point pressure at constant inlet and outlet carrier gas pressures. The optimization procedure validation was tested by the separation of 32 hydrocarbons in a column series with the aim to resolve the maximum number of components in the shortest possible analysis time.Dedicated to Professor J. F. K. Huber on the occasion of his 65th birthday     

Conjugated enynes as a new type of substrates for olefin metathesis

[reaction: see text] It has been demonstrated for the first time that conjugated enynes can be employed as a facile substrate in olefin metathesis with the use of a bispyridine-substituted ruthenium benzylidene catalyst. Cross-metathesis of the enynes with alkenes turns out to proceed with preferential formation of (Z)-isomers over (E)-isomers up to >25:1 in moderate to good yields. The intramolecular version of conjugated enynes affords novel butadienyl cycloalkenes, which are a highly useful synthetic building blocks, in acceptable yields.