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991.
Jaime González Velasco 《Central European Journal of Chemistry》2005,3(3):470-481
The analytical treatment of a model considering the electrooxidation of p-porous silicon layers under galvanostatic conditions
is able to give account of experimental facts such as the shape and location of the electroluminescence peak as well as of
the spectral shift of the electroluminescence peak produced by oxidation. The proposed model considers electroluminescence
to be the result of electron injection into the conduction band by an adsorbed intermediate produced by electrooxidation of
the surface coverage with hydrogen or siloxene of the silicon nanocrystallites. The access of holes to the surface is made
possible by low accumulation layer conditions and is the rate determining step in the electroluminescence mechanism. In this
way it is possible to give a satisfactory explanation to the shift towards the blue experimented by the electroluminiscence
emission maximum as a consequence of electrooxidation. 相似文献
992.
V. V. Barbakadze E. P. Kemertelidze I. Targamadze K. Mulkidzhanyan J. Kemink A. J. J. van den Berg K. J. Beukelman A. I. Usov 《Chemistry of Natural Compounds》2005,41(4):374-377
Two high-molecular-weight (>1000 kDa) water-soluble preparations were isolated from stems of Symphytum asperum and S. caucasicum. Their basic component was established as poly[hydroxy-1-carboxy-2-(3,4-dihydroxyphenyl)ethylene], analogous to that of high-molecular-weight
(>1000 kDa) preparations from roots of these same plants, using IR and NMR spectral data.
__________
Translated from Khimiya Prirodnykh Soedinenii, No. 4, pp. 303–305, July–August, 2005.
An erratum to this article is available at . 相似文献
993.
Wulff WD Korthals KA Martínez-Alvarez R Gómez-Gallego M Fernández I Sierra MA 《The Journal of organic chemistry》2005,70(13):5269-5277
By means of deuterium-labeling experiments, we have carried out a systematic ESI-MS study to determine the mechanism of ESI ionization of alkenyl and alkynyl group 6 Fischer carbene complexes. These compounds can be ionized under ESI conditions only in the presence of additives such as hydroquinone (HQ) or tetrathiafulvalene (TTF). Our results demonstrate that in the ESI source an anion-radical is formed after the initial HQ- or TTF-mediated electron transfer to the metallic carbene complex. For alkenyl carbene complexes, this species evolves by extrusion of a hydrogen radical to form an allenylchromium anion that is detected as the [M - H](-) ion in the mass spectrum. The preference for this mechanistic pathway could be rationalized by DFT calculations. In the case of alkynyl carbene complexes, experiments combining deuterated substrate, additive, and solvent demonstrate that the previously proposed allene-anion carbene complex is not formed. Instead, the H transfer from the ethoxy group in the anion radical, followed by extrusion of a hydrogen radical, leads to an allenyl anion that is detected in the ESI-MS as [M - H - CO](-). 相似文献
994.
2,4,6-Triaryl(thia)pyrylium salts have been used as electron-transfer photosensitizers for the cycloreversion of the oxetane ring system. The radical cation of 2,3-diphenyl-4-hydroxymethyloxetane (1) undergoes stepwise splitting via initial O-C2 cleavage. Spin and charge in the resulting intermediate are located in the oxygen and carbon atoms, respectively. Subsequent intramolecular nucleophilic attack produces 2,3-diphenyl-4-hydroxytetrahydrofuran (4a). Formation of this product occurs in the submicrosecond time scale, competing with C3-C4 cleavage to the detectable (lambdamax = 470 nm) trans-stilbene radical cation. 相似文献
995.
S. R. de Miguel G. Torres A. A. Castro O. A. Scelza 《Reaction Kinetics and Catalysis Letters》1993,51(2):443-447
The hydrogenation activity of Pt supported on activated carbon would depend on both the Pt dispersity (which can be modified by a partial carbon burn-off in air) and the impurities concentration. 相似文献
996.
Stephen de Mora Jean-Pierre Villeneuve Eric Wyse 《Accreditation and quality assurance》2007,12(11):587-592
Aspects of the International Atomic Energy Agency (IAEA) Analytical Quality Control Services (AQCS) for marine environmental
studies are discussed, focusing on recent laboratory performance studies (LPS) and the production of reference materials for
trace metals and organic compounds in various marine matrices. The IAEA has organized seventeen global interlaboratory studies
for a range of organic contaminants. Of note has been the inclusion of numerous polychlorinated biphenyl congeners (PCBs)
and some sterols of anthropogenic origin. Concurrently, there have been eleven worldwide intercomparison exercises for trace
metals in the marine environment, most of which included methylmercury. Although such interlaboratory studies can help improve
performance in individual laboratories and regional laboratory networks, the results reveal that problems remain in the determination
of some metals and many organic contaminants. 相似文献
997.
Summary. An efficient direct conversion of THP ethers into the corresponding acetates was achieved with acetic anhydride in the presence of CuSO4 · 5H2O as an available and green catalyst in high yields. 相似文献
998.
The use of fenugreek mucilage, a natural polysaccharide and a direct food additive, as a flocculating agent for removal of suspended and dissolved solids from sewage effluent has been reported. A flocculation study has been done by the standard jar test method. The percent removal of suspended solid (SS) and dissolved solid (TDS) was determined by varying the polymer dose, pH and contact time. X-ray diffraction patterns of the solid waste material of mucilage and flocs (so obtained after treatment) were used to suggest the incorporation of the crystalline waste material in the mucilage. The optimal mucilage concentration was found to be 0.16 mg/l. The suitable pH range for maximum solid removal (SS and TDS) was alkaline and the time required for treatment was 1-3 h. 相似文献
999.
Cycloreversion of 2-(p-cyanophenyl)-4-methyl-3-phenyloxetane (1) is achieved using 1-methoxynaphthalene (2) as electron-transfer photosensitizer. The experimental results are consistent with the reaction taking place from the singlet excited state of the sensitizer. Ring splitting of the radical anion 1*- occurs with cleavage of O-C2 and C3-C4 bonds, leading to products (acetaldehyde and p-cyanostilbene) different from the reagents used in the Paterno-Büchi synthesis of 1. The olefin radical anion involved in the electron-transfer process has been detected by means of laser flash photolysis. 相似文献
1000.
In the EURACHEM/CITAC draft ”Quantifying uncertainty in analytical measurement” estimations of measurement uncertainty in
analytical results for linear calibration are given. In this work these estimations are compared, i.e. the uncertainty deduced
from repeated observations of the sample vs. the uncertainty deduced from the standard residual deviation of the regression.
As a result of this study it is shown that an uncertainty estimation based on repeated observations can give more realistic
values if the condition of variance homogeneity is not correctly fulfilled in the calibration range. The complete calculation
of measurement uncertainty including assessment of trueness is represented by an example concerning the determination of zinc
in sediment samples using ICP-atomic emission spectrometry.
Received: 9 February 2002 Accepted: 17 April 2002 相似文献