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81.
N. V. Kandalintseva A. E. Prosenko O. I. Dyubchenko E. S. Stoyanov 《Russian Journal of Organic Chemistry》2001,37(9):1249-1252
A number of new S-alkylisothiuronium salts were synthesized by reaction of -[4-hydroxy(methoxy)aryl]alkyl halides with thiourea. The resulting isothiuronium salts in aqueous solution react with sodium (potassium) halides to form halogen exchange products. 相似文献
82.
A. E. Chalykh V. K. Gerasimov S. N. Rusanova O. V. Stoyanov O. G. Petukhova G. S. Kulagina S. A. Pisarev 《Polymer Science Series A》2006,48(10):1058-1066
For (ethylene-vinyl acetate copolymer)-tetraethoxysilane and (ethylene-vinyl acetate copolymer)-polydimethylsiloxane systems, the solubility of components has been studied in a wide range of temperatures and compositions. Phase diagrams have been constructed, pair interaction parameters have been calculated, and diffusion coefficients and activation energies of diffusion have been estimated. The temperature and concentration ranges of a change in solubility related to chemical interactions between the components have been revealed, and the structure of the modified copolymers has been studied. On the basis of the kinetic data on the movement of isoconcentration planes in diffusion zones of component mixing, time intervals corresponding to the onset of the chemical reaction between the components have been determined and the apparent activation energies of the process have been computed. Complex-shaped binodal and boundary curves have been interpreted within the framework of the classical Flory-Huggins theory. 相似文献
83.
Subhadeep Kal Emil Stoyanov Thomas L. Groy Ulrich Hussermann 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(10):i96-i98
Single crystals of strontium undecazinc, SrZn11, were obtained when decomposing SrZn2 under conditions of high pressure and high temperature. The new binary Sr–Zn compound crystallizes in the space group I41/amd (BaCd11 structure type) with one Sr position (m2) and three Zn sites (m2, .2/m., 1). The structure is described in terms of all‐face‐capped Zn8 tetrahedra as the central building unit, defined by the Zn atoms on .2/m. and 1. The building units are condensed into chains by the central tetrahedra sharing edges, and the chains are interconnected by shared capping atoms. The resulting three‐dimensional framework of Zn atoms yields channels that are occupied by Sr and Zn atoms on the high‐symmetry m2 positions. 相似文献
84.
Cathryn G. Conner Anka N. Veleva Vesselin N. Paunov Simeon D. Stoyanov Orlin D. Velev 《Particle & Particle Systems Characterization》2020,37(7):2000122
A highly controllable and scalable process for fabrication of large amounts of concentrated lignin nanoparticles (LNPs) is reported. These lignin core nanoparticles are formed through flash nanoprecipitation, however, scaling up of the fabrication process requires fundamental understanding of their operational formation mechanism and surface properties. It is shown how a semicontinuous synthesis system with a recirculation loop makes it possible to produce flash precipitated lignin nanoparticles in large amounts for practical applications. The roles of the process parameters, including flow rates and lignin concentration, are investigated and analyzed. The results indicate that the LNPs are formed by a process of continuous burst nucleation at the point of mixing without diffusive growth, which yields nanoparticles of highly uniform size following a modified LaMer nucleation and growth mechanism. This mechanism makes possible facile process control and scale-up. Effective control of the resulting nanoparticle size is achieved through the initial concentration of lignin in the injected solution. The impressive capability to produce suspensions of any predesigned multimodal distribution is demonstrated. The resulting nanofabrication technique can produce large volumes of concentrated LNP suspensions of high stability and tightly controlled size distributions for biological or agricultural applications. 相似文献
85.
86.
Capillary electrophoresis of peptides and proteins in isoelectric buffers: an update 总被引:2,自引:0,他引:2
Righetti PG Gelfi C Bossi A Olivieri E Castelletti L Verzola B Stoyanov AV 《Electrophoresis》2000,21(18):4046-4053
Capillary electrophoresis in acidic, isoelectric buffers is a novel methodology allowing fast protein and peptide analysis in uncoated capillaries. Due to the low pH adopted and to the use of dynamic coating with cellulose derivatives, silanol ionization is essentially suppressed and little interaction of macromolecules with the untreated wall occurs. In addition, due to the low conductivity of quasi-stationary, isoelectric buffers, high-voltage gradients can be applied (up to 800 V/cm) permitting fast peptide analysis with a high resolving power due to minimal diffusional peak spreading. Four such buffers are here described: cysteic acid (Cys-A, pI 1.85), iminodiacetic acid (IDA, pI 2.23), aspartic acid (Asp, pI 2.77) and glutamic acid (Glu, pI 3.22). A number of applications are reported, ranging from food analysis to the study of folding/unfolding transitions of proteins. 相似文献
87.
V. Yu. Ponomarev Ch. Stoyanov A. I. Vdovin 《Zeitschrift für Physik A Hadrons and Nuclei》1982,308(2):157-163
The cross section of inelastic scattering of slow electrons at large angles with excitation of high-lying 1+-states in208Pb are calculated in DWBA. The calculations are carried out both in the random-phase approximation and with the interaction of one-and two-phonon states in the framework of semi-microscopic quasi-particle-phonon model. A group of noncollective 1+-states with a large excitation probability in backward (e, é)-scattering is found in the excitation energy region of 17–21 MeV. We discuss also the problem of existence, properties, and possibility of discovery the high-lying collective 1+-states (2?ω M 1-resonance) predicted by Speth et al. 相似文献
88.
89.
M. M. El'chaninov V. M. Stoyanov A. M. Simonov B. Ya. Simkin 《Chemistry of Heterocyclic Compounds》1986,22(8):872-875
Electrophilic substitution reactions in the furylvinylbenzimidazole series were studied. In nitration, sulfonation, bromination, acylation, formylation, and hydroxymethylation reactions, the substituent enters at the -position of the furan ring. The presence of a vinylene group reduces the influence of the benzimidazole fragment on the furan ring, and therefore the reactions in the latter proceed considerably more rapidly and under milder conditions than in the case of furylbenzimidazole. Calculated data are given for the -electronic density on the carbon atoms of furyl-vinylbenzimidazole, obtained by the CNDO method.For Communication 6, see [1].Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1078–1081, August, 1986.The authors wish to express their gratitude to Yu. N. Sheinker for help in the interpretation of the PMR spectra. 相似文献
90.
It is shown using the example of polyolefin thermoplasts that the value of adhesion strength is determined by the mechanical
properties of a composition. 相似文献