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331.
Dielectric properties of plasma polymerized PVCa and composite PVCa:Au films had been analyzed in the frequency range from 10 to 105 Hz. In order to explain experimental data obtained the modification of Maxwell-Garnett and Bruggeman self-consistent models for the case of three-component composite has been done. The theoretical analysis performed allows to determine peculiarities of dielectric behavior of a three-component system, as well as to disclose the procedure of evaluation of third-component parameters. Results of this analysis are in agreement with experimental ones. 相似文献
332.
M. Chvojka B. Králiková J. Krása E. Krouský L. Láska K. Mašek O. Renner K. Rohlena J. Skála O. Štirand P. Trenda 《Czechoslovak Journal of Physics》1992,42(9):899-905
A construction and exploitation of a medium size iodine photodissociation laser system Perun II is reported. This laser produced pulses of infrared light (=1.315m) up to 50 J in energy and 300 ps in duration. The diameter of the beam is 82 mm. The beam divergence is about 4×10–4 rad. The laser beam can be focused in a focal spot of a power density exceeding 1014 W/cm2. The resuls of measurements of basic plasma parameters on an Al foil target are also presented. A recent improvement of the system includes a conversion to the second harmonic by a DKDP crystal.Presented at bilateral international seminar of High Temperature Laser Plasma and High Gain Iodine Lasers held on 4 July 1991 in the Inst. of Physics, Czechosl. Acad. Sci., in Prague (organized by Division of Optics of the Inst. of Physics, Czechosl. Acad. Sci., and Physical Section (Plasma Division) of the Union of Czech Mathematicians and Physicists. 相似文献
333.
334.
Complexes of Dioxocyanogen (OCN)2 with TiCl4 and ZrCl4 A solution of (OCN)2 was obtained by reaction of AgOCN with Br2 in H2CCl2 at ?70°C. From this the complexes TiCl4(NCO)2 and ZrCl4(NCO)2 were obtained by addition of equimolar amounts of TiCl4 and ZrCl4, respectively. According to the i.r. and Raman spectra, the (NCO)2 ligand is bonded via its N atoms to the metal. 相似文献
335.
The reversible formation of a selenenylsulfide linkage in mammalian thioredoxin reductase was identified as having a key role in its activity. Identification of selenenylsulfide and/or diselenide linkages is therefore critical to the determination of the structure and function of selenoproteins. A selenopeptide, (298)SGSAITUQCAENLPSLCSUQGLFAEEK(324) (U=selenocysteine), was isolated from a tryptic digest of rat selenoprotein P. Its two cysteine residues and two selenocysteine (Sec) residues were determined to be present in oxidized form by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS). The selenopeptide was subjected to partial reduction by dithiothreitol with immediate alkylation by iodoacetamide. This process was monitored by MALDI-TOFMS to determine the number of alkylations that had taken place. The partially reduced and alkylated peptides were then analyzed by nano-electrospray ionization tandem mass spectrometry and the results indicated that selenenylsulfide linkages Sec304-Cys314 and Cys306-Sec316 were present. It is concluded that selenoprotein P contains these two selenenylsulfide bonds. 相似文献
336.
Summary A new Schiff base ligand, N,N-bis(l-ferrocenyl-1-oxo-3-methyl)propenylethylenediamine (H2L) and its copper(II), zinc(II), cobalt(II), nickel(II), cadmium(II) and manganese(II) complexes have been prepared, and the structure of the copper complex has been determined by single crystal X-ray techniques and refined to R = 0.041 for 7403 independent reflections. The copper atom is situated in a distorted planar environment. The dihedral angle between planes of two chelating rings which do not contain the metal is 33.5°. Two substituted Cp rings are conjugated with two chelating acacim rings. The iron-centroid forms an angle of 179.4°. The Cp rings are twisted from the eclipsed conformation. 相似文献
337.
Laser emission at different wavelengths in the range of 903–914 nm and around 2.5 m has been observed upon excitation of Na2 by uv radiation from an excimer laser at 351 nm and an excimer pumped dye laser in this wavelength range. The emission is attributed to a cascade emission
followed by
. In addition, coupled with the laser emission around 910 nm, broad-band fluorescence peaking around 855.5 nm is observed which, eventually, may be the first observation of the
bound-free transition in Na2. 相似文献
338.
稀土氨基酸固体络合物的合成及结构分析进展 总被引:16,自引:2,他引:16
本文综述了稀土氨基酸络合物的合成,以及应用红外、核磁、X-射线衍射、热分析等方法进行结构分析研究的进展情况。 相似文献
339.
Treatment of the enolates of 4 generated from the asymmetric Strecker reaction products with alkyl halides or aldehydes provided the corresponding functionalized products with high diastereoselectivity. Deprotection of these products afforded the corresponding enantiopure alpha,alpha-dialkyl amino acids. 相似文献
340.
Małgorzata Pazderska-Szabłowicz Agnieszka Białkowska Ewa Kita 《Transition Metal Chemistry》2006,31(3):413-420
New chromium(III) complexes, [Cr(C2O4)2(2-hnic)]2− and [Cr(C2O4)2(3-hpic)]2− (where 2-hnic = O,O′-bonded 2-hydroxynicotinic acid and 3-hpic = N,O-bonded 3-hydroxypicolinic acid), were obtained and characterized
in solution. The acid-catalyzed aquation of the both complexes leads to liberation of the appropriate pyridinecarboxylic acid
and formation of cis-[Cr(C2O4)2(H2O)2]−. Kinetics of these reactions were studied spectrophotometrically in the 0.1–1.0 M HClO4 range, at I = 1.0 M. In the case of [Cr(C2O4)2(2-hnic)]2−, a slow chelate-ring opening at the Cr–O (phenolate) bond is followed by a fast Cr–O (carboxylate) bond breaking. The rate
law: kobs = kHQH[H+] was established, where kH is the acid-catalyzed rate constant and QH is the protonation constant of the coordinated phenolate oxygen atom. In the case of [Cr(C2O4)2(3-hpic)]2−, the reversible chelate-ring opening at Cr–N bond is followed by the rate determining step – the one-end bonded ligand liberation.
The rate law for the first step was determined: kobs = k1+k−1/Q1[H+], where k1 and k−1 are the rate constants of the chelate-ring opening and closure and Q1 is the protonation constant of the pyridine nitrogen atom. The aquation mechanisms are proposed and the effect of ligand
coordination mode on complex reactivity is discussed. 相似文献