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11.
Erdal Ertas Hakan Bildirir Onur Sahin Ipek Oksen 《Phosphorus, sulfur, and silicon and the related elements》2013,188(12):1835-1844
Abstract Syntheses of two analogues of tetrathiafulvalene (TTF), fused to 1,4-dithiin and thiophene rings, substituted with thiophene moieties, have been illustrated. The syntheses were accomplished through the reaction of a 1,8-diketone with phosphorus pentasulfide or Lawesson's reagent in boiling dry toluene. Conversion of the thioketones to their the oxo forms with mercury (II) acetate, was followed by self-coupling in freshly distilled boiling triethyl phosphite. Attempts for their electro-polymerizations through the thiophene groups at the peripherals were unsuccessful. Computational chemistry studies revealed that the thiophene groups did not exhibit enough spin densities to perform polymerization. Supplemental materials are available for this article. Go to the publisher's online edition of Phosphorus, Sulfur, and Silicon and the Related Elements to view the free supplemental file. 相似文献
12.
Ayşegül Doğan Emirhan Nemutlu M. Aykut Özek Hakan Eroğlu Sedef Kır M. Sinan Beksaç 《Chromatographia》2013,76(21-22):1513-1519
Pregnancy alters pharmacokinetic profile of many drugs, because of altering body volume and metabolism rate. Therefore, dosage rates and concentrations of drugs must be controlled during pregnancy. Here, we identified the pharmacokinetic profile of pre-operatively given cefepime in caesarean section and gynecological operations using a simple, rapid, cost-effective and valid liquid chromatographic method. The chromatographic separation was performed using 40 mM, pH 3.2 phosphate buffer containing 6 % methanol as mobile phase at 0.30 mL min?1 flow rate. Gradient elution with methanol was applied to get shorter analysis time without any interference from plasma endogens. During analyses, temperature of column, autosampler and detector were set as 30, 10 and 40 °C, respectively. The detection wavelength was 260 nm and ceftizoxime was used as internal standard. At the optimum conditions, the cefepime analysis from plasma samples was completed in 7 min. Cefepime was extracted from plasma samples using perchloric acid with a very high recovery rate (99.3 %). The method was fully validated according to the Food and Drug Administration guidelines for bioanalytical method validation, and found to be selective, linear, repeatable, reproducible and robust. After validation studies, the method was applied to five caesarean-sectioned and four non-pregnant sectioned women treated with pre-operative, prophylactic single intravenous dose of cefepime (1 g Maxipime®) in order to determine pharmacokinetic profile of cefepime. Peak serum concentrations of cefepime in caesarean-sectioned women at the arterial port after infusion was 70.11 ± 10.74 μg mL?1. The mean elimination half-life, volume of distribution and calculated area under the concentration–time curve (AUC)0–∞ were 1.10 ± 0.23 h, 14.22 ± 2.29 L and 101.55 ± 10.99 μg h mL?1 for caesarean-sectioned women; and 1.14 ± 0.21 h, 14.76 ± 2.92 L and 104.71 ± 36.34 μg h mL?1 for non-pregnant sectioned women, respectively. The area under curve, elimination half-life, maximum plasma concentration and the mean distribution volume of cefepime were not changed in case of pregnancy. 相似文献
13.
Synthesis and characterization of 4-{(E)-[(5-bromo-2-hydroxyphenyl)methylidene]amino}-N-carbamimidoylbenzene-1-sulfonamide(SA) and its composites with graphene(SA-GF) were performed. Compound SA and SA-GF were characterized by FTIR and 1H NMR. The GF dispersion in the composites was analyzed by means of scanning electron microscopy(SEM) for morphology. Thermal properties of SA and nanocomposites were investigated using differential thermal analysis(DTA) and thermogravimetric analysis(TGA). The optimum electrical conductivity of the new sulfonamide-based Schiff base was determined to be 1.78×10–5 S/cm at a frequency of 9923 Hz, an applied voltage of –19 V, a mass fraction of 9.38% for graphene loading using a central composite design in the response surface methodology. The significance of the selected parameters(frequency, voltage and GF amount) in the model was determined by the analysis of variance(ANOVA). The results showed that frequency and graphene loading represent important model terms and have considerable effects on the conductivity of SA. 相似文献
14.
Selimefendigil Fatih Öztop Hakan F. Abu-Hamdeh Nidal 《Journal of Thermal Analysis and Calorimetry》2020,141(1):465-482
Journal of Thermal Analysis and Calorimetry - Forced convection of nanofluid in a vented cavity with elastic bottom wall is studied by using an inner conductive L-shaped object and magnetic field.... 相似文献
15.
Bülbül Hakan Köysal Yavuz Doğan Onur Erman Dege Necmi Ağar Erbil 《Crystallography Reports》2019,64(3):403-406
Crystallography Reports - The title compound, C17H15NOS, crystallizes in the orthorhombic sp. gr. Pca21. Two molecules in the asymmetric unit have similar structure. Crystal structure contains weak... 相似文献
16.
In this Letter, the dynamic plane elasticity problems of 2D quasicrystals is considered. By use of the Fourier transform and matrix transformations the system is reduced to uncoupled ordinary differential equations. Fourier images of Green's functions for dynamic plane elasticity problems of 2D dodecagonal, pentagonal and decagonal quasicrystals are obtained explicitly by the suggested method. 相似文献
17.
When 7-oxodesacetamidothiocolchicine (1) was treated with various peroxides in order to afford a Baeyer-Villiger rearrangement, a complex mixture of products was formed, which included the sulfoxide, (2) and sulfone, (3). When peracetic acid was used two additional products were formed; a C-ring lactone (4) and a ring-contracted allocolchicine derivative (5). The sulfoxide (2) was semi-preparatively resolved into enantiomers by chromatography on microcrystalline triacetylcellulose. Rotational barriers around the A-C pivot bond of, and were determined by dynamic 1H NMR analysis. The compounds, and exhibit moderate inhibition of tubulin polymerization, according to in vitro turbidity studies, whereas was inactive. 相似文献
18.
In this study, a generalized method based upon nonextensive statistics is presented for nucleation and growth processes in a thin layer between two interfaces. It is shown that the presented mathematical model, which uses an index called the entropic index that measures the nonextensivity of the physical system, successfully deals with the nucleation and growth processes, and works better than Johnson–Mehl–Avrami–Kolmogorov model. The presented model also contains Austin–Rickett model as a special case. 相似文献
19.
Ozlem Yazici M. Reyhan Moroglu Husnu Cankurtaran Ozlem Cankurtaran Ferdane Karaman 《Mikrochimica acta》2008,160(4):441-445
The composites of graphite with Ardel?D-100 which is a trademark of a polyester of bisphenol-A with terephthalic and isophthalic acid were used as a sensing material
in a conductometric vapor sensor. The magnitudes of responses are increased in the order of benzene, isobutyl acetate, isoamyl
acetate, ethyl benzene and chloro benzene. This suggests that Ardel?D-100 can be used as a sensing material for chlorobenzene, ethyl benzene and isoamyl acetate. On the other hand, specific
retention volumes of the sensed vapors on Ardel?D-100 coated on graphite were determined by inverse gas chromatography at temperatures between 200 and 260 °C. The distribution
coefficient, K
s of the vapors between stationary and mobile phases in the column was obtained. It was revealed for the first time that the
logarithm of K
s of the solvents varies almost linearly with their responses based on conductometric resistance of the sensing polymer composite.
Subsequently, the study suggests that gas chromatographic retention data can be used in prediction of the conductometric responses
of a polymeric sensor to vapors.
Correspondence: Ferdane Karaman, Department of Chemistry, Yildiz Technical University, 34220 Istanbul-Esenler, Turkey 相似文献
20.
Hakan Durmaz Aydan Dag Alp Hizal Gurkan Hizal Umit Tunca 《Journal of polymer science. Part A, Polymer chemistry》2008,46(21):7091-7100
3‐Arm star‐block copolymers, (polystyrene‐b‐poly(methyl methacrylate))3, (PS‐b‐PMMA)3, and (polystyrene‐b‐poly(ethylene glycol))3, (PS‐b‐PEG)3, are prepared using double‐click reactions: Huisgen and Diels–Alder, with a one‐pot technique. PS and PMMA blocks with α‐anthracene‐ω‐azide‐ and α‐maleimide‐end‐groups, respectively, are achieved using suitable initiators in ATRP of styrene and MMA, respectively. However, PEG obtained from a commercial source is reacted with 3‐acetyl‐N‐(2‐hydroxyethyl)‐7‐oxabicyclo[2.2.1]hept‐5‐ene‐2‐carboxamide (7) to give furan‐protected maleimide‐end‐functionalized PEG. Finally, PS/PMMA and PS/PEG blocks are linked efficiently with trialkyne functional linking agent 1,1,1‐tris[4‐(2‐propynyloxy)phenyl]‐ethane 2 in the presence of CuBr/N,N,N′,N″,N″‐pentamethyldiethylenetriamine (PMDETA) at 120 °C for 48 h to give two samples of 3‐arm star‐block copolymers. The results of the peak splitting using a Gaussian deconvolution of the obtained GPC traces for (PS‐b‐PMMA)3 and (PS‐b‐PEG)3 displayed that the yields of target 3‐arm star‐block copolymers were found to be 88 and 82%, respectively. © Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 7091–7100, 2008 相似文献