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991.
Aromatic peptide nucleic acid analogs having an N-(2-aminobenzyl)glycine backbone (APNA 1) were previously identified as promising new leads for the design of polyaromatic DNA mimics. Structural modifications of 1, which lock the aromatic backbone into a unique conformation, while maintaining the same space distribution between the nucleobases as in 1, were investigated. The electrostatic potential of the aromatic backbone was also modified in an attempt to improve the solubility of these compounds in aqueous media and to evaluate how the quadrapole of the aromatic backbone may influence the biophysical properties of the APNA oligomers. PNA hexamers containing a single monomer insert of each new APNA monomer were used to explore the hybridization properties of these analogs with poly rA and poly dA. Preliminary results indicated that these modifications do not seriously alter the molecular recognition properties of APNAs towards DNA and RNA. 相似文献
992.
Tetramethyldisilane-1,2-diyl bridged Dicyclopentadienyl and Diindenyl Metal Dichlorides of the Group 4 Metals – Crystal Structure of Dicyclopentadienyl and diindenyl metal dichlorides of the type Cp′? SiMe2SiMe2? Cp′MCl2 (Cp′ = C5H4, M = Ti ( 1 ), Zr ( 2 ), Hf ( 3 ); Cp′ = C9H7, M = Zr ( 4 ), Hf ( 5 )) were synthesized and characterized by means of their 1H, 13C, 29Si-n.m.r., MS, and IR spectra. The crystal structure of 2 was determined. 相似文献
993.
A polyaluminum chloride (PAC) sample was prepared using a slow alkaline titration method. The Bio-Gel P-100 gel column chromatographic
technique was used to separate and characterize the various forms of aluminum present in the prepared PAC solution. The effluents
from a gel column were monitored using online chemical method: Al-Ferron timed complexation spectrophotometry and by 27Al nuclear magnetic resonance (NMR) spectroscopy. Effects of different experimental conditions such as eluent flow rate, ionic
strength and pH on separation of Al13 were investigated. Experimental results indicated that molecule size exclusion was not the only parameter affecting the column
chromatographic separation efficiency of Al13 but molecule charge as well. Reducing the eluent flow rate, increasing the ionic strength and suitable pH resulted in increase
in the separation efficiency. Experimental results clearly indicated that by varying the experimental conditions, it is possible
to produce pure Al13 species using a gel column chromatographic technique. 相似文献
994.
C. Santos 《European Polymer Journal》2006,42(12):3277-3285
Chitosan samples with different N-deacetylation levels were obtained from β-chitin under heterogeneous alkali conditions. Oxidative depolymerisation was performed to attain low-acetylated chitosan samples with different molecular mass. Water vapour permeability, membrane swelling and tensile mechanical properties were analysed in plasticized self-supporting chitosan membranes. The main purpose was to describe unambigously the effect of the biopolymer molecular mass and acetylation degree on these properties. Commercially available chitosan samples derived from α-chitin were also studied for comparison. The equilibrium degree of swelling in water and the water vapour permeability increase by increasing the molecular mass or the degree of acetylation. Regarding the effect on the mechanical properties, generally harder and tougher membranes were obtained for chitosans with higher molecular mass or lower acetylation degree. These observations are tentatively explained based on the different structural characteristics of the polymer and can lead to a better understanding of the tools necessary to tailor a specific type of chitosan membrane. 相似文献
995.
Donia A. M. El-Boraey H. A. El-Samalehy M. F. 《Journal of Thermal Analysis and Calorimetry》2003,73(3):987-1000
Manganese and iron complexes of Schiff bases derived from 6-formylkhellin were prepared and characterized. Complexes of o-phenylenediamine derivative (ligand (I)) are monomeric or dimeric whereas those of p-phenylenediamine derivative (ligand (II)) are polymeric. The complexes obtained are characterized by a lower magnetic moment
values. The complexes also have different solvent of crystallization with different nature of interaction. The thermal behaviour
of the ligands and their metal complexes was investigated by means of DTA, TG, IR and X-ray diffraction spectroscopy. Ligand
(I) shows different thermal behaviour from that of ligands (II) and (III). The complexes of ligand (II) give abnormal oxides
as a final product during their thermal decomposition.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
996.
997.
A novel microcalorimeter based on a miniature liquid-in-glass thermometer is described. Heat is transduced into an optical,
rather than electrical, signal, facilitating a future array format. The instrument performs batch analysis (drop mixing) with
a 2 μL sample volume. Energy changes of 4 μJ produced by a dilution of sulfuric acid are resolvable. The effect of evaporation,
and measures taken to limit it, are discussed. 相似文献
998.
文章从催化原理、制备方法、影响光/高能诱导催化反应的各种因素,提高纳米TiO2系催化剂催化活性途径及实际应用等方面,对光/高能诱导纳米TiO2及其同系物催化进行了综述。 相似文献
999.
Wiosetek-Reske AM Wysocki S Bak GW 《Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy》2005,62(4-5):1172-1178
The absorption and fluorescence spectra of N-nonyl acridine orange are determined at room temperature (298 K) in cyclohexane, benzene, carbon tetrachloride, chloroform, chlorobenzene and dichloromethane. The ground state of dipole moment was obtained by impedance measurements using Guggenheim-Debeye's method. The experimental excited state dipole moment of N-nonyl acridine orange was determined using Bakhshiev's and Kawski-Chamma-Viallet's formulae and solvent polarity parameter proposed by Reichardt. These experimental results were completed with theoretical results using quantum chemical methods. The experimental (muexp=10.76 D) and theoretical (mucal=9.9 D) dipole moments in the ground and excited state (muexp*=14.56 D) were compared. 相似文献
1000.
The 1,3-dipolar cycloaddition reactions of α-2-methoxyaryl nitrones with nitrostyrenes and chalcones have been investigated. The regiochemistry and stereochemistry of the resultant cycloadducts have been determined with the help of NMR spectroscopy and X-ray analysis. β-Nitrostyrenes add to nitrones to give two geometrical isomers, while the β-methyl-β-nitrostyrene gives a single isomer in relatively low yield. The chalcones give a single cycloadduct upon 1,3-dipolar addition. 相似文献