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11.
Hydrodynamic properties of the homologous series of the homopolymer 2-deoxy-2-methacryla-mido-D-glucose and the copolymers of 2-deoxy-2-methacrylamido-D-glucose with unsaturated acids in 0.2 M NaCl are studied via static and dynamic light scattering, viscometry, refractometry, and translational diffusion. The copolymers synthesized via the free-radical copolymerization of 2-deoxy-2-methacrylamido-D-glucose with acrylic acid or methacrylic acid contain ~20 mol % acid units. At this amount of acid units, the equilibrium rigidity of copolymer chains corresponds to that of homopolymer chains. The copolymers are distinguished by the hydrodynamic characteristics of molecules. The copolymer with methacrylic acid is similar to the homopolymer, whereas the copolymer with acrylic acid features substantially different parameters of relationships relating the hydrodynamic characteristics of homologs to their molecular masses.  相似文献   
12.
The irreversibility lines (IL) for series of Y1?xCaxBa2Cu3O7?δ (x = 0.025; 0.10 and 0.20) polycrystalline samples with different overdoping were investigated. The irreversibility fields were determined from measurements of third harmonics AC susceptibility as a function of DC field at constant temperature. For the weakly overdoped sample (with x = 0.025) Hirr(77 K) is about 7 T, which is higher than the previously reported for the non-substituted one. The irreversibility line behavior is typical for glass–liquid phase transition and this is confirmed by transport measurements. On increasing the overdoping the irreversibility fields were shifted towards lower temperatures. The behavior of Hirr(T) for the highly overdoped sample (with x = 0.20) is influenced by the surface barrier effect. It is supposed that in highly overdoped specimen the process of phase separation is enhanced and the Fermi clusters grow in size. This leads to a suppression of the bulk pinning and to a domination of the surface barrier effects and flux creep as well. As a confirmation, the obtained quadratic Jc(T) dependences were presented demonstrating the existence of S–N–S type inter-grain joints in the highly overdoped samples.  相似文献   
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14.
1.  The Al–O and P–O chemical bonds in variscite are mainly covalent in nature. The degree of covalency of the P–Ob chemical bond is substantially greater than that of Al–Ob.
2.  The presence of nonequivalent bonds of oxygen atoms in water molecules in variscite (H–OW–H) and bonds of bridge oxygen atoms (P–Ob–Al) leads to splitting of the 02s and 02p states of the OW and Ob atoms amounting to 7 eV.
3.  The strength of the Al–OW bond is considerably lower than that of the Al–Ob bond.
4.  The H11, H21, and H22 hydrogen atoms form hydrogen bonds with the bridge oxygen atoms, but H12 does not participate in hydrogen bonding.
5.  The results from cluster calculations of the electronic structure of variscite provide a basis for interpreting the experimental x-ray photoelectron spectrum and for determining the influence of structural molecules of water on the XPS line shape and structure.
Institute of Chemistry, Ural Branch, Academy of Sciences of the USSR. Translated from Zhurnal Strukturnoi Khimii, Vol. 32, No. 5, pp. 17–22, September–October, 1991.  相似文献   
15.
The compositions of the lipids and fatty acids of the seeds ofCynoglossum officinale, familyBoraginaceae have been established. The bulk of the lipids consisted of netural compounds (95.2%), while the amounts of glycolipids and phospholipids were 3.1 and 1.7%, respectively. Among the fatty acids, in addition to the usual components, acids characteristic for theBoraginaceae family have been found: 18:3 (6, 9, 12), 18:3 (9, 12, 15), 18:4 (6, 9, 12, 15), 20:1 (11), 22:1 (13), and 24:1 (15). Institute of the Chemistry of Plant Substances, Uzbek Academy of Sciences, Tashkent. South Urals Reservation, Bashkir. Institute of Chemistry, Bashkir Scientific-Center, Urals Branch, Russian Academy of Sciences, Ufa. Translated from Khimiya Prirodnykh Soedinenii, No. 6, pp. 758–762, November–December, 1991.  相似文献   
16.
By the peptide map method, a phosphorylated peptide has been isolated from a tryptic hydrolysate of phosphorylated yeast inorganic pyrophosphatase (I), and this is a direct proof of the formation of a covalent bond between (I) and phosphate in the course of this reaction. The isolation and analysis of the peptide from the tryptic hydrolysate shows that the phosphate acceptor is probably the aspartic acid residue 240 or 248. Analysis of a tryptic hydrolysate of (I) modified with O-phosphoethanolamine has shown that O-phosphoethanolamine forms an amide bond with the carboxy group of the same aspartic acid residue. In an alkaline medium, the phosphate residue migrates to the imidazole ring of a histidine residue, apparently that present in position 222.  相似文献   
17.
Let be an entire function of finite type with respect to finite order and let be a subset of an open cone in a certain n-dimensional subspace (the smaller , the sparser ). We assume that this cone contains a ray 0} \right\}$$ " align="middle" border="0"> . It is shown that the radial indicator of at any point may be evaluated in terms of function values at points of the discrete subset . Moreover, if tends to zero fast enough as over , then this function vanishes identically. To prove these results, a special approximation technique is developed. In the last part of the paper, it is proved that, under certain conditions on and , which are close to exact conditions, the function bounded on is bounded on the ray.  相似文献   
18.
Russian Physics Journal - An approach to inkjet printing of low-viscosity liquids is suggested consisting in suppression of undesirable weakly damped acoustic oscillations under the action of a...  相似文献   
19.
Summary A study was made of the hydration of tertiary diacetylenic glycols under the action of aqueous dimethylamine solution, which leads to substituted 3(2H)-furanones. Under the conditions of acid hydration, 2-methyl-3,5-hexadiyn2-ol also gives the corresponding furanone.  相似文献   
20.
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