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排序方式: 共有129条查询结果,搜索用时 437 毫秒
121.
A novel fluorescent reagent for hydroperoxides, 4-(2-diphenylphosphinoethylamino)-7-nitro-2,1,3-benzoxadiazole (1), was developed on the basis of the method for designing photoinduced electron transfer (PET) reagents having a benzofurazan skeleton. Compound 1 was quantitatively reacted with hydroperoxides to give its fluorescent derivative, 2. In acetonitrile, the Phi value (0.44) of 2 was 31 times greater than that of 1. The long excitation (458 nm) and emission (520 nm) wavelengths of 2 are suitable for the determination of hydroperoxides, especially in biosamples. [structure: see text] 相似文献
122.
V. Lavayen N. Mirabal M.A. Santa Ana C.M. Sotomayor Torres 《Applied Surface Science》2007,253(12):5185-5190
This work reports the successful realization of MoS2 nanotubes by a novel intercalation chemistry and hydrothermal treatment. An inorganic-organic precursor of hexadecylamine (HDA) and molybdenum disulphide (MoS2) were used in synthesizing the nanocomposite comprising laminar MoS2 with HDA intercalated in the interlaminar spacing. The formation of MoS2 nanotubes occurred during hydrothermal treatment (HT) by a self-organized rolling mechanism. The nanotubes were observed to have dimensions 2-12 m in length and inner diameters typically in the range of 25-100 nm. We also report the formation of amorphous nanocoils of MoS2 obtained during similar procedures. 相似文献
123.
Santa T Al-Dirbashi OY Ichibangase T Fukushima T Rashed MS Funatsu T Imai K 《Biomedical chromatography : BMC》2007,21(11):1207-1213
The applicability of benzofurazan derivatization regents to carboxylic acids analysis in LC/ESI-MS/MS (high-performance liquid chromatography/electrospray ionization tandem mass spectrometry) was examined. The product ion spectra of DAABD-AE {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(2-aminoethylamino)-2,1,3-benzoxadiazole}, DAABD-PZ {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-N-piperazino-2,1,3-benzoxadiazole}, DAABD-PiCZ {4-[4-carbazoylpiperidin-1-yl]-7-[2-(N,N-dimethylamino)ethylaminosulfonyl]-2,1,3-benzoxadiazole}, DAABD-ProCZ {4-[2-carbazoylpyrrolidin-1-yl]-7-[2-(N,N-dimethylamino) ethylaminosulfonyl]-2,1,3-benzoxadiazole} and DAABD-Apy {4-[2-(N,N-dimethylamino)ethylaminosulfonyl]-7-(3-aminopyrrolidin-1-yl)-2,1,3-benzoxadiazole}, and their acetylated compounds were obtained. An intense fragment ion at m/z 151 corresponding to (dimethylamino)ethylaminosulfonyl moiety was observed in each spectra, suggesting that these reagents were suitable for ESI-MS/MS analysis. DAABD-AE, DAABD-APy and DAABD-PZ were applied to the analysis of octanoic acid and it was found that DAABD-AE and DAABD-APy gave high signal intensity suitable for LC/ESI-MS/MS. 相似文献
124.
Gita Sakale Maris Knite Valdis Teteris Velta Tupureina Santa Stepina Elina Liepa 《Central European Journal of Physics》2011,9(2):307-312
Polymer-nanostructured carbon composites (PNCC) using three different polymers as composite matrix materials (polyvinylacetate
(PVAc), polyethylene glycol (PEG) and ethylene-vinylacetate copolymer (EVA)) have been developed. High structure carbon black
Printex XE2 (Degussa AG) was used as a composites filler. Ethanol vapour sensor-effect of composites was determined as a change
of electrical resistance as the composite was held in ethanol vapour for 30 seconds. Reversibility of electrical resistance
of PNCC, response stability and repeatability have been measured and compared. The electrical resistance response of EVA-nanostructured
carbon composite (EVA-NCC) to ethanol vapour as a function of vinylacetate content in the copolymer has been evaluated. Promising
ethanol vapour sensor-effect has been observed for PEG-NCC followed by PVAc-NCC and EVA-NCC. 相似文献
125.
Santa GL Bernardino SM Magalhães S Mendes V Marques MP Fonseca LP Fernandes P 《Applied biochemistry and biotechnology》2011,165(1):1-12
The present work aims to provide the basic characterization of sol–gel immobilized inulinase, a biocatalyst configuration
yet unexploited, using as model system the hydrolysis of inulin to fructose. Porous xerogel particles with dimensions in slight
excess of 10 μm were obtained, yielding an immobilization efficiency of roughly 80%. The temperature– and pH–activity profiles
displayed a broader bell-shaped pattern as a result of immobilization. In the latter case, a shift of the optimal pH of 0.5
pH units was observed towards a less acidic environment. The kinetic parameters estimated from the typical Michaelis–Menten
kinetics suggest that immobilization in sol–gel did not tamper with the native enzyme conformation, but on the other hand,
entrapment brought along mass transfer limitations. The sol–gel biocatalyst displayed a promising operational stability, since
it was used in more than 20 consecutive 24-hour batch runs without noticeable decay in product yield. The performance of sol–gel
biocatalyst particles doped with magnetite roughly matched the performance of simple sol–gel particles in a single batch run.
However, the operational stability of the former proved poorer, since activity decay was evident after four consecutive 24-hour
batch runs. 相似文献
126.
Otaciro R. Nascimento Claudio J. Magon Jose Fernando Lima Jose Pedro Donoso Eglantina Benavente Jaime Paez Vladimir Lavayen Maria Angelica Santa Ana Guillermo Gonzalez 《Journal of Sol-Gel Science and Technology》2008,45(2):195-204
In this work we report results from continuous-wave (CW) and pulsed electron paramagnetic resonance (EPR) and proton nuclear
magnetic resonance (NMR) studies of the vanadium pentoxide xerogel V2O5:nH2O (n ≈ 1.6). The low temperature CW-EPR spectrum shows hyperfine structure due to coupling of unpaired V4+ electron with the vanadium nucleus. The analysis of the spin Hamiltonian parameters suggests that the V4+ ions are located in tetragonally distorted octahedral sites. The transition temperature from the rigid-lattice low-temperature
regime to the high temperature liquid-like regime was determined from the analysis of the temperature dependence of the hyperfine
splitting and the V4+ motional correlation time. The Electron Spin Echo Envelope Modulation (ESEEM) data shows the signals resulting from the interaction
of 1H nuclei with V4+ ions. The modulation effect was observed only for field values in the center of the EPR absorption spectrum corresponding
to the single crystals orientated perpendicular to the magnetic field direction. At least three protons are identified in
the xerogel by our magnetic resonance experiments: (I) the OH groups in the equatorial plane, (ii) the bound water molecules
in the axial V=O bond and (iii) the free mobile water molecules between the oxide layers. Proton NMR lineshapes and spin-lattice
relaxation times were measured in the temperature range between 150 K and 323 K. Our analysis indicates that only a fraction
of the xerogel protons contribute to the measured conductivity. 相似文献
127.
Tsukamoto Y Santa T Yoshida H Miyano H Fukushima T Hirayama K Imai K Funatsu T 《Biomedical chromatography : BMC》2006,20(10):1049-1055
The combined use of a so-called internal standard and the isotope-labeled derivatization reagent for the quantification of analytes for liquid chromatography-mass spectrometry (LC/MS) was further studied. The sample solution (containing the analytes and an internal standard) was derivatized with the light form of the derivatization reagent, 7-(N,N-dimethylaminosulfonyl)-4-(aminoethyl)piperazino-2,1,3-benzoxadiazole (DBD-PZ-NH(2)) or 7-(N,N-dimethylaminosulfonyl)-4-piperazino-2,1,3-benzoxadiazole (DBD-PZ). A standard solution of the analytes (containing an internal standard) was derivatized with the isotope (d(6))-labeled derivatization reagent, DBD-PZ-NH(2) (D) or DBD-PZ (D), and served as the isotope-labeled internal standards. The peak heights of the targeted analytes derivatives in the sample solution were corrected using those of the internal standard and the heavy form derivatives of the standards, and the calibration curves were constructed. The curve bending of the calibration curves caused by the ion suppression at the ion source was suppressed and the linear dynamic ranges of the calibration curves were expanded. The derivatives of DBD-PZ-NH(2) were about 10 times more sensitively detected than those of DBD-PZ derivatives and, therefore, DBD-PZ-NH(2) might be suitable for sensitive detection. 相似文献
128.
Ciapina EM Melo WC Santa Anna LM Santos AS Freire DM Pereira N 《Applied biochemistry and biotechnology》2006,131(1-3):880-886
The production of biosurfactant by Rhodococcus erythropolis during the growth on glycerol was investigated. The process was carried out at 28 degrees C in a 1.5-L bioreactor using glycerol as carbon source. The bioprocess was monitored through measurements of biosurfactant concentration and glycerol consumption. After 51 h of cultivation, 1.7 g/L of biosurfactant, surface, and interfacial tensions values (with n-hexadecane) of 43 and 15 mN/m, respectively, 67% of Emulsifying Index (E (24)), and 94% of oil removal were obtained. The use of glycerol rather than what happens with hydrophobic carbon source allowed the release of the biosurfactant, originally associated to the cell wall. 相似文献
129.
Claramunt RM Santa María MD Sanz D Alkorta I Elguero J 《Magnetic resonance in chemistry : MRC》2006,44(5):566-570
Three N-substituted pyrazoles and three N-substituted indazoles [1-(4-nitrophenyl)-3,5-dimethylpyrazole (1), 1-(2,4-dinitrophenyl)-3,5-dimethylpyrazole (2), 1-tosyl-pyrazole (3), 1-p-chlorobenzoylindazole (4), 1-tosylinda-zole (5) and 2-(2-hydroxy-2-phenylethyl)-indazole (6)] have been studied by NMR spectroscopy in solution (1H, 13C, 15N) and in the solid state (13C, 15N). The chemical shifts have been compared with GIAO/DFT calculated absolute shieldings. Some discrepancies have been analyzed. 相似文献