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131.
Abstract

The synthesis and structure of N-D-pentopyranosylamines derived from the amines tiyptamine tyramine and the pentoses D-xylose, D-arabinose and D-lyxose are presented. NMR spectroscopy and mass spectrometry were used to verify the proposed α,β-D-pentopyranosylamine structures.  相似文献   
132.
We consider the integral means for the class of functions which are meromorphic and univalent in an annulus.  相似文献   
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The present work reports semiconducting properties of high purity TiO2 determined in the gas/solid equilibrium, as well as during controlled heating and cooling in the range 300–1,273 K. The activation energy of the electrical conductivity is considered in terms of the activation enthalpy of the formation of ionic defects and the activation enthalpy of the mobility of electronic defects. These data, determined from the dynamic electrical conductivity experiments, are compared to the electrical conductivity data determined in equilibrium. It is shown that only the equilibrium electrical conductivity data for high-purity TiO2 are well defined. It is shown that the activation energy of the electrical conductivity determined in equilibrium differs substantially from that for the dynamic electrical conductivity data during cooling and heating. It is concluded that the formation enthalpy term determined from the dynamic conductivity data is determined by the heating/cooling rate rather than materials’ properties.  相似文献   
136.
The kinetics of condis (conformationally disordered) crystal formation from the melt and of rigid crystals from condis crystals has been studied by differential scanning calorimetry for trans-1,4-polybutadiene and polytetrafluoroethylene. Generally very low two-stage Avrami exponents between 0.02 and 1.74 were needed to describe the fast and often incomplete crystallizations. None of the commonly accepted crystal nucleation and growth models seems to fit the data.  相似文献   
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The average unit cell approach has been successfully used to construct the probability distributions of atomic distances from the reference lattice points and to calculate the diffraction patterns for decorated Fibonacci chains with non-Fibonacci type of decoration. General method able to distinguish between various quasilattice decorations has been elaborated and tested for decorated Fibonacci chains. Financial support from the Polish Committee for Sci. Research under grant No. 2 P03B 041 16 is acknowledged. Presented at the DI-CRM Workshop held in Prague, 18–21 June 2000.  相似文献   
139.
A hydroxylactone ((1R,5S)‐1‐hydroxy‐3,6‐dioxabicyclo [3.2.1] octan‐2‐one, abbreviated as LAC) obtained from catalytic pyrolysis of cellulose was investigated as a monomer in the synthesis of polyesters by ring‐opening polymerization (ROP) with L ‐lactide. Although stannous octoate resulted inactive, ROP initiated by zirconium (IV) acetylacetonate afforded novel copolyesters from LAC and lactide mixtures in the bulk at 110 °C. Copolymers were obtained with different LAC content (from 19 to 45%) with a random microstructure as established by detailed NMR analysis. FTIR spectrometry confirmed the presence in the polymer chain of the OH groups originally present in LAC, which do not react during polymerization due to steric hindrance and inter/intramolecular hydrogen bonding. Reaction with trichloroacetylisocyanide proved that OH groups of the polyesters can be readily derivatized. The application of LAC as a comonomer enables the insertion of the alcohol functionality in polylactide avoiding protection/deprotection steps and potentially expanding the realm of biomaterials affordable from carbohydrate feedstock. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 247–257, 2009  相似文献   
140.
Voltammetric and microscopic data on the analytical properties of small iridium-based (127- μm diameter) mercury film electrodes are presented. A method of estimating and controlling the size of the deposit is described. The voltammetric behaviour of electrodes with mercury deposits varying from a film to a near-hemisphere is discussed for linear-scan, differential- and normal- pulse voltammetry. The systems Pb2+/Pb, Fe3+/Fe2+ and Co2+/Co, are used to show that, by changing the size of the deposit, either time-dependent or almost time-independent (steady-state) voltammograms can be obtained under the same instrumental conditions. Possible applications to the determination of high concentrations of depolarizers are outlined; voltammetric data for the determination of lead in the range 10–120 mM are presented. The evaluation of diffusion coefficients is discussed.  相似文献   
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