17 research outputs found

    ΠŸΡ€ΠΈΠΌΠ΅Π½Π΅Π½ΠΈΠ΅ ΠΏΠ»ΡƒΡ‚ΠΎΠ½ΠΈΠΉ-содСрТащСго Ρ‚ΠΎΠΏΠ»ΠΈΠ²Π° Π² Ρ€Π΅Π°ΠΊΡ‚ΠΎΡ€Π΅ Π’Π’Π­Π 

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    РасчСт нСйтронно–физичСских ΠΏΠ°Ρ€Π°ΠΌΠ΅Ρ‚Ρ€ΠΎΠ² Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΠΉ Π·ΠΎΠ½Ρ‹ ядСрного водо–водяного Ρ€Π΅Π°ΠΊΡ‚ΠΎΡ€Π°, оптимизация Ρ‚ΠΎΠΏΠ»ΠΈΠ²Π½ΠΎΠΉ ΠΊΠΎΠΌΠΏΠΎΠ·ΠΈΡ†ΠΈΠΈ для Ρ€Π΅Π°ΠΊΡ‚ΠΎΡ€Π° ВВЭР–1000, провСсти расчСт нСйтронно–физичСских ΠΏΠ°Ρ€Π°ΠΌΠ΅Ρ‚Ρ€ΠΎΠ² Π°ΠΊΡ‚ΠΈΠ²Π½ΠΎΠΉ Π·ΠΎΠ½Ρ‹ ядСрного водо–водяного Ρ€Π΅Π°ΠΊΡ‚ΠΎΡ€Π°.Π‘alculate the neutron-physical parameters of the core of a nuclear water-water reactor, optimize the fuel composition for the VVER-1000 reactor, and calculate the neutron-physical parameters of the core of a nuclear water-water reactor

    Nuclear-physical methods of analysis using spectrometric radiation sources

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    To analyze the nuclear-physical methods of elemental composition and distribution of impurities by the method of Rutherford backscattering, the 238Pu source was used as the source of ionizing radiation. It was shown that in the absence of an accelerator this method is promising, since it allows one to monitor the composition and distribution of elements during technological processes

    Selbstorganisation von Helicaten und molekularen Tetraedern

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    In this research hierarchical multi component self-assembly processes were investigated. The two ligands 2,3-dihydroxybenzaldehyde and 2,3-dihydroxyacetophenone were used for the multistep self-assembly of helicate-type dinuclear titanium(IV) or gallium(III) complexes in the presence of lithium ions. Further more, coordination studies with linear dicatechol diimine ligands, which possess due to the variation of the spacer different geometrical and electronical properties, were made. An enantiomerically pure dinuclear triple-stranded titanium(IV) helicate is formed from a dicatechol diimine ligand with an (R,R)-1,2-diaminocyclohexane spacer and its stereochemical features were elucidated by experimental and theoretical methods. By the complexation of a ligand which possesses C2h symmetry in its idealized structure with titanium(IV), homochiral helicates were diastereoselectively formed. On the other hand a ligand with idealized C2v symmetry leads with surprisingly high selectivity to the formation of the heterochiral meso-helicate. It could be shown, that a rigid connector transfers the stereochemical information of the first complex unit to a stereo-controlling unit, that is located at a distance of about 1 nm from the complex moiety. The small central unit influences the stereochemistry at the second titanium(IV) triscatecholate complex, which again is located 1 nm away. Thus, the stereochemical information is transferred over a distance of nearly 2 nm. Further on, the synthesis of linear ligands with a 2,2’-bipyridine and a dicatechol-unit with different binding sites were described. Thereby the 5,5’-diamino-2,2’-bipyridine was transformed into the imine- or amide-bridged dicatechol-bipyridine ligands. Coordination studies have shown, that it’s possible to selectively choose one of the binding sites by the choice of appropriate metal-ions. A series of triscatechols with an idealized axis of C3-symmetrie were synthesized. Hereby amide, imine or direct bonds are introduced as linkage between the catechol units and various C3-symmetric backbones. Their metal complexes with Ti(IV)ions were investigated. For the first time we succeeded to obtain a molecular tetrahedron with four Ti(IV)ions, which was big enough to bind guests in its interior. It could be shown, that the use of a flexible triscatecholate ligand with a C3-symmetrie leads to a dynamic combinatorial library. The dynamic library of complexes is formed in DMF in the presence of potassium cations. From this library three different coordination compounds can be selected by additi on of an appropriate template, by crystallization, or by equilibration of the mixture in DMSO

    Π—Π° ΠΊΠ°Π΄Ρ€Ρ‹. 1938. β„– 28 (219)

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    Π—Π° дальнСйший подъСм Π² Ρ€Π°Π±ΠΎΡ‚Π΅ ΠΏΡ€ΠΎΡ„ΡΠΎΡŽΠ·ΠΎΠ²Πž ростС ΠΏΠ°Ρ€Ρ‚ΠΈΠΈ / Ал. Π¨.Агитационная Ρ€Π°Π±ΠΎΡ‚Π° Π½Π° 10-ΠΌ участкС / А. Π‘.ΠŸΡ€ΠΈΠ²Π΅Ρ‚ΡΡ‚Π²ΡƒΠ΅ΠΌ Ρ‚ΠΈΠΏΠΎΠ²Ρ‹ΠΉ устав Π²Ρ‹ΡΡˆΠ΅ΠΉ ΡˆΠΊΠΎΠ»Ρ‹ / Π’. Π‘ΠΎΡ€ΠΎΠ΄ΠΈΠ½ [ΠΈ Π΄Ρ€.]Комсомол пополняСтся ΠΏΠ΅Ρ€Π΅Π΄ΠΎΠ²ΠΎΠΉ молодСТью / Π›-овДоска ΠΏΠΎΡ‡Π΅Ρ‚Π° ΠΈΠΌΠ΅Π½ΠΈ 20-лСтия Π’Π›ΠšΠ‘ΠœΠ’Ρ‹ΠΏΠΎΠ»Π½ΡΡŽΡ‚ ΠΎΠ±ΡΠ·Π°Ρ‚Π΅Π»ΡŒΡΡ‚Π²ΠΎ / А. Π€Π΅Π΄ΠΎΡ€Π΅Π½ΠΊΠΎΠ Π°Π·Π²Π΅Ρ€Π½ΡƒΡ‚ΡŒ социалистичСскоС сорСвнованиС ΠΌΠ΅ΠΆΠ΄Ρƒ Π³Ρ€ΡƒΠΏΠΏΠ°ΠΌΠΈ / Π—Π°Ρ€ΠΈΠ½ΠŸΠΎΡ‡Π΅ΠΌΡƒ Π·Π°ΠΊΡ€Ρ‹Ρ‚ мСдицинский ΠΏΡƒΠ½ΠΊΡ‚? / А. Π€.Π‘Π΄Π΅Π»Π°Ρ‚ΡŒ Π³Π°Π·Π΅Ρ‚Ρƒ ΠΎΠ±Ρ€Π°Π·Ρ†ΠΎΠ²ΠΎΠΉΠž ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½ΠΈΠΈ Π²Ρ‹Π±ΠΎΡ€ΠΎΠ² руководящих ΠΊΠΎΠΌΡΠΎΠΌΠΎΠ»ΡŒΡΠΊΠΈΡ… ΠΎΡ€Π³Π°Π½ΠΎΠ². ΠŸΠΎΡΡ‚Π°Π½ΠΎΠ²Π»Π΅Π½ΠΈΠ΅ ЦК Π’Π›ΠšΠ‘ΠœΠ˜Π½ΡΡ‚Ρ€ΡƒΠΊΡ†ΠΈΠΈ ΠΎ ΠΏΡ€ΠΎΠ²Π΅Π΄Π΅Π½ΠΈΠΈ Π²Ρ‹Π±ΠΎΡ€ΠΎΠ² руководящих ΠΊΠΎΠΌΡΠΎΠΌΠΎΠ»ΡŒΡΠΊΠΈΡ… ΠΎΡ€Π³Π°Π½ΠΎΠ²ΠŸΡ€ΠΈΠ²Π»Π΅Ρ‡ΡŒ ΠΊ отвСтствСнности Π±Π΅Π·Π·Π°Π±ΠΎΡ‚Π½Ρ‹Ρ… Ρ€ΡƒΠΊΠΎΠ²ΠΎΠ΄ΠΈΡ‚Π΅Π»Π΅ΠΉΠ‘ΠΊΠΎΡ€ΠΎ-Π»ΠΈ Π±ΡƒΠ΄Π΅Ρ‚ Π½Π°Π²Π΅Π΄Π΅Π½ порядок Π² ΠΎΠ±Ρ‰Π΅ΠΆΠΈΡ‚ΠΈΠΈ? / Π’ΡƒΠ±ΠΎΠ»ΡŒΡ†Π΅Π²Π Π°ΡΠΏΠΈΡΠ°Π½ΠΈΠ΅ составлСно ΠΏΠ»ΠΎΡ…ΠΎ / ΠœΠ°ΠΌΠ°Π΅Π²Π°Π›ΡŽΠ±ΠΈΡ‚Π΅Π»ΠΈ Π²ΠΎΠ»ΠΎΠΊΠΈΡ‚Ρ‹Π•Π΄ΠΈΠ½Ρ‹ΠΉ ΠΊΠ°Π»Π΅Π½Π΄Π°Ρ€Π½Ρ‹ΠΉ ΠΏΠ»Π°Π½ Ρ€Π°Π±ΠΎΡ‚Ρ‹ ΠΎΡ€Π³Π°Π½ΠΈΠ·Π°Ρ†ΠΈΠΉ Вомского ΠΈΠ½Π΄ΡƒΡΡ‚Ρ€ΠΈΠ°Π»ΡŒΠ½ΠΎΠ³ΠΎ института / МамаСваО Ρ€Π°Π±ΠΎΡ‚Π΅ ΠΈΠ½Ρ„ΠΎΡ€ΠΌΠ°Ρ†ΠΈΠΎΠ½Π½ΠΎ - библиографичСского ΠΎΡ‚Π΄Π΅Π»Π° / Π’. Π›Π΅Ρ‚ΡƒΠ½ΠΎΠ²Π¨Π°Ρ…ΠΌΠ°Ρ‚Ρ‹ / Π›. ΠŸΠΎΡΡ‚Π½ΠΈΠΊΠΎ
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