A new approach to the total synthesis of (±)‐20‐ epidasycarpidone

In this study, a new synthetic route to the total synthesis of (±)‐20‐ epidasycarpidone (1b) is described. This route involves acid catalyzed ring closure and the formation of the intermediate 13 in the key step. The relative stereochemistry of 13 has been confirmed by X‐ray structure analysis. The tetracyclic intermediate 13 was synthesized through several steps starting from 3. The removal of the protecting group of 13 yielded the lactam 15, which was reduced by Red‐Al® to give 16. The synthesis of (±)‐20‐ epidasycarpidone (1b) was finally completed by the oxidation of 16.     

1,3‐Dibenzoylimidazolidine‐2‐thione and 1,3‐dibenzo­yl‐3,4,5,6‐tetra­hydro­pyrimidine‐2(1H)‐thione

The title compounds, 1,3‐dibenzo­ylimidazolidine‐2‐thione, C₁₇H₁₄N₂O₂S, (I), and 1,3‐dibenzo­yl‐3,4,5,6‐tetra­hydro­pyrimidine‐2(1H)‐thione, C₁₈H₁₆N₂O₂S, (II), were obtained from the reactions of imidazolidine‐2‐thione and 1,4,5,6‐tetra­hydro­pyrimidine‐2‐thiol, respectively, with benzoyl chloride. Compounds (I) and (II) contain, respectively, imidazolidinethione [C=S = 1.6509 (14) Å] and ­pyrimidinethione [C=S = 1.6918 (19) Å] moieties bonded to two benzoyl rings. The mol­ecules of (I) exhibit C₂ symmetry, the C=S bond lying along the twofold rotation axis, while the mol­ecules of (II) have mirror symmetry (C_s). The imida­zolidine ring in (I) is essentially planar, while the pyrimidine ring in (II) adopts a boat conformation. Mol­ecules of (I) are linked by weak inter­molecular C—H⋯O inter­actions, while mol­ecules of (II) are held together by van der Waals inter­actions.     

Long Afterglow Room‐Temperature Phosphorescence from Nanopebbles: A Urea Pyrolysis Product

Materials having long afterglow are highly sought after for various applications such as light‐emitting diodes, security signs and bioimaging. Herein, we report a simple, low‐cost synthesis of a purely organic room‐temperature phosphorescent nanomaterial with a pebble‐like structure by heating urea, a biocompatible and easily available precursor, at 200 °C with a high phosphorescence lifetime of 1.0365 s and a visible afterglow for up to 10 s. This urea derived phosphorescent nanocomposite (UPNC) can be mixed with commercially available acrylic paint base and common gum, which can be readily used as a phosphorescent pigment.     

On 4-transitivity in the Moufang plane

The purpose of this paper is to give a short proof of 4-transitivity in Moufang planes. This proof originated in the observation of the two first name authors that the standard Moufang identities, together with the identity (1) x^–1(y(xz)) = (x^–1(yx)z, which is asserted in [2, p. 103] to hold in Cayley-Dickson division algebras, can be applied to give a particularly simple algebraic proof of the fact that the collineation group of a Moufang plane is transitive on four-points. Unfortunately, as pointed out by H. Karzel and demonstrated here in Proposition 1, (1) does not hold in Cayley-Dickson algebras. Nevertheless, the algebraic proof of transitivity remains valid after slight modifications and is given here as Theorem 1.The authors wish to thank Professor Karzel for pointing out the error in [2] and for his suggestions in preparing the final version of this paper.Dedicated to Professor H. Karzel on the occasion of his 60th birthday.     

Enhanced optical oxygen sensing using a newly synthesized ruthenium complex together with oxygen carriers

In this article, an emission based, simple and fast method is proposed for the determination of gaseous oxygen. A newly synthesized fluorophore, dichloro-{2,6-bis[1-(4-dimethylamino-phenylimino) ethyl]pyridine}ruthenium(II) has been used for oxygen sensing together with oxygen carrier perfluorochemicals (PFCs) in silicon matrix. It should be noted that the solubility of oxygen in fluorocarbons is about three to ten times large as that observed in the parent hydrocarbons or in water, respectively. Employed PFCs are chemically and biochemically inert, have high dissolution capacities for oxygen, and, once doped into sensing film, considerably enhance the response of sensing agent.     

Solid-phase extraction of bismuth, lead and nickel from seawater using silica gel modified with 3-aminopropyltriethoxysilane filled in a syringe prior to their determination by graphite furnace atomic absorption spectrometry

In this study, the use of syringe filled with sorbent for the separation and enrichment of bismuth, lead and nickel prior to their analysis by graphite furnace atomic absorption spectrometry was described to substitute for batch and column techniques. The method proposed in this paper was compared with column technique with respect to easiness, fastness, simplicity, recovery and risk of contamination. The syringe was filled with 0.5 g of sorbent and in order to retain the analyte elements, 5 ml of sample solution (pH≥5) was drawn into the syringe to 15 s and discharged again in 15 s. Then, 2.0 M of HCl, as the eluent, was drawn into the syringe and ejected back to desorb the analyte elements. At optimum conditions, the recoveries of Bi, Pb and Ni were 95-99% with relative standard deviations (RSDs) of around ±2%. Detection limit (δ) was 0.5 μg l⁻¹ for Bi, Pb and Ni, respectively. The elements could be concentrated by drawing and discharging several portions of sample successively but eluting only one time. Bi, Pb and Ni added to a seawater sample were quantitatively recovered (>95%) with low RSD values of around ±2-3%. The risk of contamination is less than that with the column technique. In addition, it is much faster, simpler, easier, more practical and handy compared with column technique.     

Investigation of the structural and thermal properties of Y,Ag and Ce-assisted SiO<Subscript>2</Subscript>–Na<Subscript>2</Subscript>O–CaO–P<Subscript>2</Subscript>O<Subscript>5</Subscript>-based glasses derived by sol–gel method

A glass with the composition of the SiO₂–Na₂O–CaO–P₂O₅ was synthesized by sol–gel method at temperature of 900 °C, and then yttrium-, silver- and cerium-containing glasses were prepared at the same conditions using this base system. The structural and thermal properties of the glass samples were investigated by X-ray diffraction, Fourier transform infrared (FTIR) spectroscopy, scanning electron microscopy, energy-dispersive X-ray (EDX) spectroscopy and differential thermal analysis techniques. The Ca₅(PO₄)₂(SiO₄)₆ phase having the orthorhombic crystal system is detected for each sample without any secondary phase, and this phase is confirmed by the FTIR spectra. With the addition of Y, Ag and Ce to the SiO₂–Na₂O–CaO–P₂O₅ system, the variations in the average crystallite size, crystallinity percent, lattice parameters and unit cell volume are observed. A decrease in the crystallization peak temperature and the changes in the glass transition temperature are seen with the addition of Y, Ag and Ce to the base system. The addition of Y, Ag and Ce to the base glass increases significantly its density. The EDX spectra of the as-prepared samples verify the introduction of the as-mentioned elements.     

Surface structure and photoluminescence properties of AZO thin films on polymer substrates

Al‐doped zinc oxide (AZO) thin films were deposited on indium tin oxide (ITO) coated polyethylene terephthalate (PET) substrates by radio frequency (RF) magnetron sputtering method at room temperature. The effects of film thickness on the surface structure and the photoluminescence properties of the films were investigated by atomic force microscopy (AFM), secondary ion mass spectroscopy (SIMS) and room temperature photoluminescence (PL). AFM analysis showed that the surface of all films was extremely flat and uniform at nanoscale. Root mean square (RMS) value of the surface roughness which scanned the surface area of 3 µm by 3 µm and grain size increased with increasing the film thickness. Thus, the surface morphology of the films became rough because of the coarse grains. The depth profile of AZO layers was analyzed by SIMS. It was found that the thickness of the AZO layer is almost same with the desired film thickness. The PL intensity of the dominant peak decreased and shifted slightly towards the shorter wavelengths with increasing the film thickness. According to the relationships between luminescence intensity and crystalline characteristics, it was observed that the intensity of the peak decreased by the increased surface area of the grains. Copyright © 2014 John Wiley & Sons, Ltd.     

Mechanical,electronic and optical properties of SeZnO3: a GGA+U study

ABSTRACT

Based on first principles computations, the structural, mechanical, electronic band structure, and optical properties of SeZnO₃ compound have been predicted. The dependence of selected observables of SeZnO₃ compound on the effective U (the Hubbard on-site Coulomb repulsion) parameter has been investigated in detail. The elastic constant, Young’s modulus, bulk modulus, shear modulus, Poisson ratio, anisotropic factor, acoustic velocity, and Debye temperature have been computed. The calculated electronic band structure and density of states indicate that SeZnO₃ is a semiconductor material and has indirect band gap. The computations of the optical spectra, as a function of the incident photon radiation in 0–35?eV energy range has also been performed and the interband transitions are examined. The results indicate that Hubbard parameter plays a crucial role in explaining mechanical, electronic, and optical properties of SeZnO₃.