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1.
To assess the character of packing of double-stranded (ds) DNA molecules in liquid-crystalline dispersion particles formed by phase exclusion of DNA molecules from aqueous salt solutions of poly(ethylene glycol), the circular dichroism spectra of these dispersions at different temperatures have been compared. It has been shown for the first time that heating dispersion particles with the hexagonal packing of ds-DNA molecules is accompanied by the hexagonal → cholesteric phase transition. This result can be described using the notion of quasi-nematic layers composed of orientationally ordered adjacent ds-DNA molecules in the structure of dispersion particles; these layers can be packed in two ways dictating their hexagonal or cholesteric spatial structure.  相似文献   
2.
This article describes the state of and progress in experimental studies of liquid crystals of naturally occurring nucleic acids and synthetic polynucleotides. The areas considered in this review include: (i) the liquid-crystalline phase of nucleic acids in aqueous salt solutions, (ii) the liquid-crystalline phase of nucleic acids in aqueous polymer solutions, (iii) the liquid-crystalline phase of nucleic acids in living systems. Some unsolved problems which are of interest from both a physicochemical and a biological point of view are discussed.  相似文献   
3.
Different strategies in design of nanoconstructions whose building blocks are both linear molecules of double-stranded nucleic acids and nucleic acid molecules fixed in the spatial structure of particles of liquid crystalline dispersions have been considered.  相似文献   
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5.
Certain physicochemical characteristics of particles of the cholesteric liquid-crystal dispersions of complexes of double-stranded nucleic acids with rare earth elements have been determined. It is shown for the first time that the binding of the rare earth cations to linear nucleic acid molecules ordered in the structure of particles of the cholesteric liquid crystal dispersions is accompanied not only by amplification of the abnormal band in the circular dichroism spectrum, but also by the disappearance of the characteristic maximum on the X-ray scattering curves for small angles. The (cholesteric 1-cholesteric 2) transition induced by rare earth cations is an example of the operation of a microscopic machine consisting of spatially ordered nucleic acid molecules. Particles of the cholesteric liquid crystal dispersions of nucleic acid complexes with rare earth elements hold the abnormal optical properties for a long time.  相似文献   
6.
CD spectra of liquid-crystalline dispersions, X-ray diffraction patterns and optical textures of liquid crystals prepared from native superhelical DNA in poly(ethyleneglycol)-containing water-salt solutions before and after treatment of DNA with micrococcal nuclease have been obtained. It was found that condensation of native superhelical DNA is accompanied by the formation of liquid crystals with a non-specific optical texture. After treatment of the DNA, liquid-crystalline dispersions, with Micrococcal nuclease the DNA is able to form two similar types of liquid crystals with abnormal optical activity which differ in the peculiarities of their textures. The data obtained demonstrate the formation of multiple types of liquid crystals from high molar mass double-stranded optically active DNA molecules.  相似文献   
7.
A streamlined method has been developed for the isolation and analysis of polycyclic aromatic hydrocarbons in avian blood cells and plasma utilizing quick, easy, cheap, effective, rugged, and safe extraction in combination with novel phospholipid cleanup technology. A variety of traditional extraction and cleanup techniques have been employed in the preparation and analysis of polycyclic aromatic hydrocarbonsin a variety of matrices; liquid–liquid partitioning, solid‐phase extractions, gel permeation chromatography, and column chromatography are all effective techniques, however they are laborious and time consuming processes that require large amounts of solvent. Using quick, easy, cheap, effective, rugged, and safe extraction coupled with phospholipid cleanup, samples can be quickly screened while maintaining high throughput and sensitivity. With a liquid chromatography approach, analysis times may be kept short at 16 min while maintaining high analyte recovery. Recoveries in quality control samples ranged from 70 to 109%, with average surrogate recoveries of 80.6 ± 1.10%. The result of using a quick, easy, cheap, effective, rugged, and safe extraction approach in conjunction with phospholipid cleanup is a methodology that significantly reduces sample preparation time and solvent use while maintaining high sensitivity and reproducibility.  相似文献   
8.
The temperature dependence of the electrical conductivity and pyroelectric coefficient of lithium niobate crystals reduced in a hydrogen atmosphere has been studied. It has been established that the activation energy of dark electrical conduction in these crystals in the temperature range 288?C350 K differs from the corresponding values for crystals reduced in vacuum and is equal to 0.68 ± 0.02 eV. It has been shown that the annealing of LiNbO3 crystals in a hydrogen atmosphere hardly affects their pyroelectric properties. The mechanism of electrical conduction of LiNbO3 crystals reduced in a hydrogen-containing atmosphere has been discussed.  相似文献   
9.
Optics and Spectroscopy - Circular dichroism (CD) spectra of liquid crystalline dispersions formed as a result of phase exclusion of double-stranded DNA molecules from aqueous-salt-poly(ethylene...  相似文献   
10.
The possible positions of H+ ions in stoichiometric crystals of lithium niobate are analyzed using computer simulation. It is shown that all hypothetical positions of H+ ions at the midpoints of the O-O bonds are unstable and must be excluded from further consideration. An analysis of the trajectories of displacement of H+ ions in the structure of LiNbO3 shows that an H+ ion is associated with one of the O2? ions of the upper oxygen face of the NbO6 octahedron and that the direction of the dipole moment of the OH? group differs only slightly from the direction of the short O-O bond.  相似文献   
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