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951.
Nikos G. Tsierkezos 《Journal of solution chemistry》2007,36(10):1301-1310
The reduction of benzophenone (Bzph) in 3-pentanone (PEN), acetone (ACE), N,N-dimethylacetamide (DMA), N,N-dimethylformamide (DMF), tetrahydrofuran (THF), acetonitrile (ACN) and dimethyl sulfoxide (DMSO) with n-tetrabutylammonium hexafluorophosphate (TBAPF6) as background electrolyte was studied using the technique of cyclic voltammetry at the temperature of 263.15 K. The half-wave
potentials (E
1/2) were extracted. The reduction of Bzph occurs in two successive one-electron steps to produce first the free radical anion
Bzph− and then the dianion Bzph2−. The results indicated that the radical anion Bzph− is reoxidized to Bzph in all investigated solvent media whereas the dianion Bzph2− is reoxidized to Bzph− only in THF. The heterogeneous electron-transfer rate constants (k
s
) were evaluated by employing the electrochemical rate equation proposed by Nicholson. The rate of electron transfer for the
Bzph/Bzph− couple was found to be relatively slow in all investigated solvent media. Consequently, the electron-transfer processes can
be recognized as quasi-reversible. The diffusion coefficients (D) of Bzph in the investigated solvent media have been calculated using the modified Randles-Sevcik equation. The effect of
the physical and chemical properties of the solvent medium on the electrochemical behavior of Bzph has been examined. 相似文献
952.
Advanced oxidation processes for decolorization of aqueous solution containing acid red G azo dye 总被引:2,自引:0,他引:2
Some investigations concerning the decolorization of Acid Red G azo dye by photooxidation with hydrogen peroxide were performed.
The influences of pH, oxidant concentration, and the presence of Fe2+ or other metal ions (Co2+, Cu2+, Ni2+, Mn2+) as potential catalysts, were investigated. The best results were obtained in the presence of ferrous ions in acid and neutral
media. The other ions are not as effective as Fe2+ for dye decolorization. Co2+ and Cu2+ ions have a catalytic action, at low concentration, within a wide range of pH. Ni2+ and Mn2+ ions have no catalytic effect in photooxidation with hydrogen peroxide at acid Ni2+ and Mn2+ ions have no catalytic effect in photooxidation with hydrogen peroxide at acid pH values, but show a weak action in alkaline
media. 相似文献
953.
A. V. Makarycheva-Mikhailova S. I. Selivanov N. A. Bokach V. Yu. Kukushkin P. F. Kelly A. J. L Pombeiro 《Russian Chemical Bulletin》2004,53(8):1681-1685
Reactions of the platinum(IV) nitrile complexes [PtCl4(RCN)2] (R = Me, CH2Ph, Ph) with 1,2- and 1,4-PhS(=NH)C6H4SPh in CH2Cl2 afforded addition products of sulfimides and coordinated nitriles, viz., the [PtCl4{NH=C(R)N=S(Ph)(C6H4SPh)}2] complexes. The latter were isolated in 75—90% yields and characterized by elemental analysis, positive-ion FAB mass spectrometry, IR spectroscopy, and 1H and 13C1H NMR spectroscopy. The temperature dependence of the 1H NMR spectra of the model [PtCl4{NH=C(R)N=SPh2}2] complexes (R = Me, Et) in CD2Cl2 studied in a temperature range from +40 to -70 °C demonstrated that E—Z isomerization of the ligands is a dynamic process in a range from +40 to -10 °C. The activation free energy of this process was calculated.Published in Russian in Izvestiya Akademii Nauk.
Seriya Khimicheskaya, No. 8, pp. 1618–1622, August, 2004. 相似文献
954.
The synthesis of [Mn12O12(O2CMe)6(p-CO2-phenyl nitronyl nitroxide)10(H2O)4]· 4H2O, (1), by direct replacement of some of the acetate groups in [Mn12O12(O2CMe)16(H2O)4] · 4H2O · 2MeCO2H, (2), with the organic radical p-HO2C-phenyl nitronyl nitroxide, (3), is reported. E.p.r. spectra show exchange narrowing in (1) due to coupling between the manganese ions and radicals. The isotropic hyperfine splitting constant from the manganese ions is a = 96 Oe at 5.5K. The magnetic susceptibility indicates antiferromagnetic exchange interactions between the manganese ions and the radicals with the Weiss constant = -25 K. The spin was determined to be S = 6 from magnetization data in the 2--30 K temperature range at 50 kOe, suggesting a mixture of ground state with excited states. 相似文献
955.
Addition–elimination reactions involving a nucleophile and a remote leaving group [SH
N(AE)tele] are well-known under basic conditions, especially amongst electron-poor six-membered heterocycles, but are less commonly
encountered for five-membered heterocycles and are rare under acidic conditions. Concentrated HCl converts 1-hydroxy-1H-pyrazolo[3,4-c] isoquinoline and 1-hydroxy-1H-pyrazolo[3,4-c]quinoline into 3-chloro-1H-pyrazolo[3,4-c]isoquinoline and 3-chloro-1H-pyrazolo[3,4-c]quinoline, respectively. However, apparently neither the isomeric 1-hydroxy-1H-pyrazolo[4,3-c](iso)-quinolines nor the parent 1-hydroxypyrazole undergo this reaction. Additionally, all these systems are refractory under
basic conditions. We present a plausible mechanism for the reaction, involving the 3-addition of Cl- to the diprotonated heterocycle, followed by the elimination of water. Calculations of the initial transition states and
intermediates, using optimisation at B3LYP/6-311+G(d,p), including thermochemistry [HF/6-31+G(d)], and single-point Poisson–Boltzmann
self-consistent reaction field determination of the free energy of solvation (Jaguar Poisson–Boltzmann self-consistent reaction
field), support this mechanism and reproduce the observed order of reactivity, the addition step being 2–4 kcal less favourable
for the isomeric 1-hydroxy-1H-pyrazolo[4,3-c](iso)quinolines and provide a rationalisation for the role of strong acid.
Received: 27 June 2002 / Accepted: 6 September 2002 /
Published online: 14 February 2003 相似文献
956.
Smith CJ Huang W Walcott CJ Turner W Grainger J Patterson DG 《Analytical and bioanalytical chemistry》2002,372(1):216-220
For measurement of biomarkers from polycyclic aromatic hydrocarbon (PAH) exposure, an analytical method is described quantifying hydroxylated PAH (OH-PAH) in urine samples. This method determined monohydroxy metabolites of naphthalene, fluorene, phenanthrene, fluoranthene, pyrene, chrysene, benzo[c]phenanthrene, and benz[a]anthracene. The sample preparation consisted of enzymatic hydrolysis, solid-phase extraction and derivatization with a silylating reagent. Five carbon-13 labeled standards were used for isotope dilution. Analytes were separated by gas chromatography (GC) and quantified with high-resolution mass spectrometry (HRMS). This method produced good recoveries (41-70%), linearity, and specificity. Data were corrected for blank levels from the naphthalene, fluorene, and phenanthrene metabolites. Method detection limits ranged from 2 ng L(-1) for 1-hydroxypyrene to 43.5 ng L(-1) for 1-hydroxynaphthalene. Using quality control charts from two urine pools, the method can be readily applied to biomonitoring PAH exposure. 相似文献
957.
Érika Pinto Marinho A. G. Souza Danniely S. de Melo Iêda M. G. Santos Dulce M. A. Melo Walquíria J. da Silva 《Journal of Thermal Analysis and Calorimetry》2007,87(3):801-804
Because
of their electrical, magnetic and catalytic properties rare earth and transition
metal mixed oxides are important compounds. Lanthanum chromites have been
extensively used as solid oxide fuel cell (SOFC) interconnect materials. In
this work, lanthanum chromites partially substituted by alkaline earth metals
were synthesized by the urea combustion process. TG and DSC techniques were
used to evaluate the presence of the organic material in the powder after
reaction on the hot plate. The powders were calcinated at 900°C and characterized
by XRD and SEM. The results show that the particles have nanometric dimensions
and the perovskite structure was formed. 相似文献
958.
A major issue with the electrolytic conductivity measurement for pure water is the lack of standard or reference methods.
A primary method traceable to SI and suitable for pure-water conductivity measurement was developed at the Physikalisch-Technische
Bundesanstalt (PTB), Germany, as the base for the calibration method for the conductivity measuring devices at the low conductivity
level. This paper provides a novel method to calculate the bulk resistance of pure water using impedance measured at a single
frequency, which is one of the key procedures for the primary methods. 相似文献
959.
Fumio Kiyono Hideo Tajima Keiichi Ogasawara Akihiro Yamasaki 《Fluid Phase Equilibria》2005,230(1-2):90-98
A method for determining quadruple points of a two-component system containing a simple hydrate phase is proposed. This method utilizes the quasi-static change of the system along three-phase equilibrium lines and was proved to be able to determine the quadruple points as accurately as the conventional method. By using this method, even though some preparation is necessary, a quadruple point can be determined in just a single experimental run. The behavior of the system near the quadruple points was also examined experimentally, for both the quasi-static and the irreversible change cases. At the quadruple points, the temperature and pressure of the system were kept constant for a while, as at the triple point of water. In both cases, the representative point of the state of the system passed through the quadruple point on a p–T diagram. 相似文献
960.
Three novel heteropolytungstates, [Cu(phen)2]4[α-SiW12O40] (1), [Cu4(4,4′-bpy)3(2,2′-bpy)4][α-SiW12O40] · H2O (2) and [Cu(4,4′-bpy)(4,4′-Hbpy)0.5]2[PW12O40] (3) (phen = 1,10-phenanthroline, 4,4′-bpy = 4,4′-bipyridine, 2,2′-bpy = 2,2′-bipyridine), have been synthesized and characterized
by elemental analyses, IR, TG analyses and single-crystal X-ray diffraction. Compound (1) exhibits interesting chiral layer constructed from interperpendicular helical chains running along a crystallographic 21 axis in the c and a directions. Furthermore, the chiral layers are connected by the [α-SiW12O40]4− anions via hydrogen bonding interactions to form a 3D superamolecular structure. The [Cu4(4,4′-bpy)3(2,2′-bpy)4]4+ coordinated complexes in compound (2) are packed together via the aromatic π–π stacking interactions and exhibit an interesting 3D sandglasslike “host” network with 1D channels, in which
[α-SiW12O40]4− anions “guests” reside. Compound (3) has a unique 2D superamolecular network, which is composed of cationic CuI coordination polymer chains and discrete [PW12O40]3− polyoxoanions as linkers. It is noteworthy that the monprotonated 4,4′-bpy ligands of (3) act as arms and connect the adjacent 2D network, generating a 3D interpenetrating superamolecular structure. 相似文献