Novel Naphthalimide Derivatives as Selective G-Quadruplex DNA Binders

A new derivate of 4-bromo-1,8-naphthalic anhydride and its quaternized analogue have been prepared and characterized. The interactions of both derivatives with human telomere quadruplex-DNA and ds-DNA have been comparatively studied by UV-visible (UV-Vis), fluorescent intercalator displacement assays, competition dialysis, circular dichroism (CD), agarose gel electrophoresis, and polyacrylamide gel electrophoresis. The results show that both derivatives can stabilize G-quadruplexes DNA, and they show different binding affinities for G-quadruplexes-DNA and ds-DNA. All spectroscopic studies have shown that the derivatives have a modest selectivity for G-quadruplex versus ds-DNA.     

Recovery of Au(III) ions by Au(III)-imprinted hydrogel

A new Au(III)-imprinted hydrogel (Au(III)-Imp) was prepared by the photopolymerisation of 4-acryloylmorpholine (AcM), 2-hydroxyethyl acrylate (HEA), and poly(ethylene glycol) diacrylate (cross-linking monomer, PEG-DA) in the presence of gold ions. In addition, non-imprinted hydrogel (N-Imp) was similarly prepared without Au(III) ions The Au(III)-Imp hydrogel was characterised by several techniques. To achieve the optimal conditions, effect of pH, time, and initial metal ion concentrations were investigated using a batch system. The pre-concentration factor for Au(III) ions was found to be at least 100. The analytical parameters of the method were determined and the method was also successfully applied to computer circuit board scrap samples. The reusability of the Au(III)-Imp hydrogel was also determined.     

On Pell Quaternions and Pell-Lucas Quaternions

The main object of this paper is to present a systematic investigation of new classes of quaternion numbers associated with the familiar Pell and Pell-Lucas numbers. The various results obtained here for these classes of quaternion numbers include recurrence relations, summation formulas and Binet’s formulas.     

Diels‐alder click reaction for the preparation of polycarbonate block copolymers

The Diels‐Alder reaction as a click reaction strategy is applied to the preparation of well‐defined polycarbonate (PC)‐block copolymers. A well‐defined α‐anthracene‐terminated polycarbonate (PC‐anthracene) is prepared using 9‐anthracene methanol as an initiator in the ring opening polymerization of benzyl 5‐methyl‐2‐oxo‐1,3‐dioxane‐5‐carboxylate in CH₂Cl₂ at room temperature for 5 h. Next, a well‐defined α‐furan protected maleimide‐terminated‐poly(ethylene glycol) (PEG₁₁‐MI or PEG₃₇‐MI), ‐poly(methyl methacrylate) (PMMA₂₆‐MI), and ‐poly(ε‐caprolactone) (PCL₂₇‐MI) were clicked with the PC‐anthracene at reflux temperature of toluene to yield their corresponding PC‐based block copolymers (PC‐b‐PEG, PC‐b‐PMMA, and PC‐b‐PCL). The homopolymer precursors and their block copolymers were characterized by using the GPC, NMR and UV analysis. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013     

Measurements of indoor radon concentration levels in Kilis,Osmaniye and Antakya,Turkey during spring season

The fact that 50% of the natural radiation dose to which humans are exposed is caused by radon gas makes indoor radon measurements important. In this study, levels of indoor radon gas were measured in 204 houses in Kilis, Osmaniye and Antakya using passive nuclear track detectors. Cr-39 radon detectors were left in the living rooms of participants’ houses, then analyzed at the Radon Laboratory of Health Physics Department in Çekmece Nuclear Research and Training Center (ÇANEM) of Atomic Energy Agency of Turkey (TAEK). Average indoor radon activity concentrations for Kilis, Osmaniye and Antakya were 50 Bq/m³ (1.26 mSv/y), 51 Bq/m³ (1.29 mSv/y) and 40 Bq/m³ (1.01 mSv/y), respectively.     

Optimal exercise of jointly held real options: A Nash bargaining approach with value diversion

This paper provides a two-stage decision framework in which two or more parties exercise a jointly held real option. We show that a single party’s timing decision is always socially efficient if it precedes bargaining on the terms of sharing. However, if the sharing rule is agreed before the exercise timing decision is made, then socially optimal timing is attained only if there is a cash payment element in the division of surplus. If the party that chooses the exercise timing can divert value from the project, then the first-best outcome may not be possible at all and the second-best outcome may be implemented using a contract that is generally not optimal in the former cases. Our framework contributes to the understanding of a range of empirical regularities in corporate and entrepreneurial finance.     

Comparative characterisation of zinc oxide thin films prepared from zinc acetate with or without water of hydration via the sol–gel method

Zinc oxide thin films were prepared using either zinc acetate dihydrate or anhydrous zinc acetate via the sol–gel method. Comparative characterisation of the crystallographical, morphological, optical/spectroscopical and electrical properties of the so-obtained films was performed. The idea of one- (in the case of the anhydrous precursor), and two- (in the other case) stage hydrolysis/condensation was postulated, which was supported by the characterisation results. The film prepared using the anhydrous precursor had a more pronounced c-axis crystal orientation preference, with a larger average crystallite size and more porous morphology. The transparency of this film was significantly lower over the UV/visible region due to its more porous morphology, which also resulted in lower intensity of the ‘near band edge emission’, and higher electrical resistivity. The overall results also suggested that anhydrous zinc acetate could be employed as a precursor for the sol–gel synthesis of zinc oxide thin films, which might have potential advantages in microelectronic and optoelectronic applications.     

Synthesis and characterization of new metal-free and metallophthalocyanines fused α-methylferrocenylmethoxy units

Synthesis of metal-free and metallophthalocyanines bearing α-methylferrocenylmethoxy units was described. Precursor 3 required for the preparation of phthalocyanines 4–9, was synthsized by the nucleophilic aromatic substitution reaction between α-methylferrocenylmethanol and 4-nitrophthalonitrile in dry DMF. The metal-free phthalocyanine 4 was prepared from 4-(α-methylferrocenylmethoxy)phthalonitrile 3 in 1-pentanol with a catalytic amount of 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU). Metallophthalocyanines (M = Zn, Cu, Co, Ni and Pb) were prepared by cyclotetramerization reaction of phthalonitrile with appropriate materials. The phthalonitrile, metal-free and metallophthalocyanines were characterized by ¹H and ¹³C NMR, FT-IR UV–Vis and mass spectral data, as well as elemental analyses, which were consistent with the proposed structures.     

Antibacterial glass films prepared on metal surfaces by sol–gel method

This paper describes the preparation and characterization of glass films consisting of SiO₂, Li₂O, Na₂O, K₂O or MgO in varying compositions on stainless steel and aluminum substrates by sol–gel method. Silver phosphate or silver incorporated zeolite was also introduced into the sols for obtaining antibacterial effect. The SiO₂/Li₂O/Na₂O system having the composition of 85:5:10 wt% was found as the optimum for obtaining a stable sol and film formation. The films were investigated by scanning electron microscopy (SEM) and electron dispersive analysis by X-ray (EDX), Fourier transformed infrared (FTIR) spectroscopy, thermo-gravimetric analysis (TGA) and differential thermal analysis (DTA). Homogenous films having 300 ± 20 nm thicknesses were formed by spin coating and then by curing at 500 °C for 1 h. Obtained films had high adherence to the metal substrates and they were also durable in acidic, basic or NaCl environments. They also presented a powerful antibacterial effect against E. coli.     

Sol–gel derived mesoporous and microporous alumina membranes

Stable polymeric and colloidal boehmite sols were prepared by sol–gel process through controlled hydrolysis/condensation reactions. The particle sizes of the colloidal sols were in the 12–25 nm range depending on the process parameters and about 2 nm for polymeric sols. The presence of a significant increase in the microporosity content of the heat treated polymeric membranes relative to the mesoporous colloidal membranes might make the design of thermally stable microporous alumina membranes with controlled pore structures possible. The phase structure evolution in the 600–800 °C range had shown that the crystallization of the gamma alumina in the amorphous matrix starts at about 800 °C. This indicated that the pore structure stability may be enhanced through processing up to this relatively high temperature in polymeric alumina derived unsupported membranes. The permeance values of the two and three layered colloidal alumina membranes were observed to be independent of pressure which implies that the dominant gas transport mechanism is Knudsen diffusion in these structures. This was also supported by the 2.8 nm BJH pore sizes of the colloidal membranes. The Knudsen diffusion equation derived permeances of the polymeric alumina membranes with thicknesses of about 300 nm were determined to be very close to the experimentally determined permeance values.