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排序方式: 共有136条查询结果,搜索用时 15 毫秒
1.
E. G. Berezhko L. T. Ksenofontov 《Journal of Experimental and Theoretical Physics》1999,89(3):391-403
The kinetic theory of regular acceleration of cosmic rays in supernova remnants is used to investigate the expected chemical
composition of the rays. It is shown that the shapes of the calculated profiles of the chemical elements making up the cosmic
rays are consistent with experiment wherever the results of measurements are available. The acceleration process is accompanied
by relative enrichment of the cosmic rays with heavy elements. If the analogous property of the mechanism underlying the injection
of superthermal particles into the acceleration regime is taken into account, such enrichment supports the formation of the
required composition of cosmic rays in the energy range up to 1014–1015 eV.
Zh. éksp. Teor. Fiz. 116, 737–759 (September 1999) 相似文献
2.
L. N. Vasilevskaya V. S. Vasil’eva N. A. Shkredova A. S. Khatenko M. A. Ksenofontov D. S. Umreiko 《Journal of Applied Spectroscopy》2005,72(1):142-145
The spectral-structural characteristics of polyurethane compositions with antipyrene fillers were investigated by a method of IR spectroscopy. The changes revealed in the vibrational spectra can be caused by intermolecular interaction of oligoether and diphenylmethane diisocyanate with aluminum-, boron-, and phosphor-containing compounds.__________Translated from Zhurnal Prikladnoi Spektroskopii, Vol. 72, No. 1, pp. 133–135, January–February, 2005. 相似文献
3.
4.
Alexander A. Ksenofontov Galina B. Guseva Svetlana A. Stupikova Elena V. Antina 《Journal of fluorescence》2018,28(2):477-482
In this paper, we report on the results of spectrofluorimetric study of new fluorescent sensor based on [Zn2L2] doped in ethyl cellulose. The sensor optical signal is based on the rapid fluorescence quenching in the presence of acetone vapor. The acetone vapor detection limit in a gas mixture by means of sensor based on [Zn2L2] doped in ethyl cellulose is 1.68 ppb. Being highly sensitive to the acetone acetone presence, instant in response and easy to use, the sensor can find an application for the noninvasive diagnostics of diabetes as well as for the monitoring of the content of acetone acetone in the air at industrial and laboratory facilities. 相似文献
5.
E. Yu. Borovikova D. A. Ksenofontov Yu. K. Kabalov V. S. Kurazhkovskaya S. Yu. Stefanovich I. V. Korchemkin E. A. Asabina 《Crystallography Reports》2012,57(4):514-520
A complex study of the synthetic CsMgPO4 phosphate with a ??-tridymite structure type is performed. It is found that CsMgPO4 is an unstable phase. At room temperature in air, it absorbs water and turns into the CsMgPO4 · 6H2O crystal hydrate. The transformation of cubic CsMgPO4 · 6H2O into orthorhombic CsMgPO4 proceeds upon heating to 150°C by the pattern of the first-order phase transition with the dehydration of the specimen. 相似文献
6.
Ksenofontov S. Yu. Terpelov D. A. Gelikonov G. V. Shilyagin P. A. Gelikonov V. M. 《Radiophysics and Quantum Electronics》2019,62(2):151-158
Radiophysics and Quantum Electronics - We study the causes of artifact appearance in the images obtained by the method of spectral domain optical coherence tomography with parallel reception of the... 相似文献
7.
Gaspar Ana B. Ksenofontov Vadim Spiering Hartmut Reiman Sergey Real José A. Gütlich Philipp 《Hyperfine Interactions》2002,144(1-4):297-306
This article reports on the study of the interplay between magnetic coupling and spin transition in 2,2′-bipyrimidine (bpym)-bridged
iron(II) dinuclear compounds. Coexistence of both phenomena has been observed in [Fe(bpym)(NCS)2]2bpym, [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym (bpym = 2,2′-bipyrimidine, bt = 2,2′-bithiazoline) by the action of external physical factors namely pressure or electromagnetic
radiation. Competition between magnetic exchange and spin crossover has been studied in [Fe(bpym)(NCS)2]2bpym at 6.3 kbar. LIESST experiments carried out in [Fe(bpym)(NCSe)2]2bpym and [Fe(bt)(NCS)2]2bpym at 4.2 K have shown that is possible to achieve dinuclear molecules with different spin states in this class of compounds.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
8.
H. Spiering V. Ksenofontov O. Leupold J. Kusz L. Deák Z. Németh C. Bogdán L. Bottyán D. L. Nagy 《Hyperfine Interactions》2016,237(1):58
The effect of selfabsorption in Mössbauer sources is studied in detail. Spectra were measured using an old 57 C o/R h source of 74M B q activity with an original activity of ca. 3.7G B q and a 0.15G B q 57 C o/α ? F e source magnetized by an in-plane magnetic field of 0.2 T. The 57 C o/α ? F e source of a thickness of 25 μ was used both from the active and the inactive side giving cause to very different selfabsorption effects. The absorber was a single crystal of ferrous ammonium sulphate hexahydrate (FAS). Its absorption properties were taken over from a detailed study (Bull et al., Hyperfine Interact. 94(1–3), 1; Spiering et al. 2). FAS (space group P21/c) crystallizes as flat plates containing the (\(\overline {2}\)01) plane. The γ-direction was orthogonal to the crystal plate. The 57 C o atoms of the 57 C o/R h source were assumed to be homogeneously distributed over a 6μ thick Rh foil and to follow a one dimensional diffusion profile in the 25 μ Fe-foil. The diffusion length was fitted to 10 μ. The theory follows the Blume-Kistner equations for forward scattering (Blume and Kistner, Phys. Rev. 171, 417, 3) by integrating over the source sampled up to 128 layers. 相似文献
9.
Seredyuk M Gaspar AB Ksenofontov V Galyametdinov Y Kusz J Gütlich P 《Journal of the American Chemical Society》2008,130(4):1431-1439
Three types of interplay/synergy between spin-crossover (SCO) and liquid crystalline (LC) phase transitions can be predicted: (i) systems with coupled phase transitions, where the structural changes associated to the Cr<-->LC phase transition drives the spin-state transition, (ii) systems where both transitions coexist in the same temperature region but are not coupled, and (iii) systems with uncoupled phase transitions. Here we present a new family of Fe(II) metallomesogens based on the ligand tris[3-aza-4-((5-C(n))(6-R)(2-pyridyl))but-3-enyl]amine, with C(n) = hexyloxy, dodecyloxy, hexadecyloxy, octadecyloxy, eicosyloxy, R = hydrogen or methyl (C(n)-trenH or C(n)-trenMe), which affords examples of systems of types i, ii, and iii. Self-assembly of the ligands C(n)-trenH and C(n)-trenMe with Fe(A)2 x xH2O salts have afforded a family of complexes with general formula [Fe(C(n)-trenR)](A)2 x sH2O (s > or = 0), with A = ClO4(-), F-, Cl-, Br- and I-. Single-crystal X-ray diffraction measurements have been performed on two derivatives of this family, named as [Fe(C6-trenH)](ClO4)2 (C(6)-1) and [Fe(C6-trenMe)](ClO4)2 (C(6)-2), at 150 K for C(6)-1 and at 90 and 298 K for C(6)-2. At 150 K, C(6)-1 displays the triclinic space group P, whereas at 90 and at 298 K C(6)-2 adopts the monoclinic P2(1)/c space group. In both compounds the iron atoms adopt a pseudo-octahedral symmetry and are surrounded by six nitrogen atoms belonging to imino groups and pyridines of the ligands C(n)-trenH and C(n)-trenMe. The average Fe(II)-N bonds (1.963(2) A) at 150 K denote that C(6)-1 is in the low-spin (LS) state. For C(6)-2 the average Fe(II)-N bonds (2.007(1) A) at 90 K are characteristic of the LS state, while at 298 K they are typical for the high-spin (HS) state (2.234(3) A). Compound C(6)-1 and [Fe(C18-trenH)](ClO4)2 (C(18)-1) adopts the LS state in the temperature region between 10 and 400 K, while compound C(6)-2 and [Fe(Cn-trenMe)](ClO4)2 (n = 12 (C(12)-2), 18 (C(18)-2)) exhibit spin crossover behavior at T(1/2) centered around 140 K. The thermal spin transition is accompanied by a pronounced change of color from dark red (LS) to orange (HS). The light-induced excited spin state trapping (LIESST) effect has been investigated in compounds C(6)-2, C(12)-2 and C(18)-2. The T(1/2)LIESST is 56 K (C(6)-2), 48 K (C(16)-2), and 56 K (C(18)-2). On the basis of differential scanning calorimetry, optical polarizing microscopy, and X-ray diffraction findings for C(18)-1, C(12)-2, and C(18)-2 at high temperature a smectic mesophase SX has been identified with layered structures similar to C(6)-1 and C(6)-2. The compounds [Fe(C(n)-trenH)](Cl)2 x sH2O (n = 16 (C(16)-3, s = 3.5, C(16)-4, s = 0.5, C(16)-5, s = 0), 18 (C(18)-3, s = 3.5, C(18)-4, s = 0.5, C(18)-5, s = 0), 20 (C(20)-3, s = 3.5, C(20)-4, s = 0.5, C(20)-5, s = 0)) and [Fe(C18-tren)](F)2 x sH2O (C(18)-6, s = 3.5, C(18)-7, s = 0) show a very particular spin-state change, while [Fe(C18-tren)](Br)2 x 3H2O (C(18)-8) together with [Fe(C18-tren)](I)2 (C(18)-9) are in the LS state (10-400 K) and present mesomorphic behavior like that observed for the complexes C(18)-1, C(12)-2, and C(18)-2. In compounds C(n)-3 50% of the Fe(II) ions undergo spin-state change at T(1/2) = 375 K induced by releasing water, and in partially dehydrated compounds (s = 0.5) the Cr-->SA phase transition occurs at 287 K (C(16)-4), 301 K (C(18)-4) and 330 K (C(20)-4). For the fully dehydrated materials C(n)-5 50% of the Fe(II) ions are in the HS state and show paramagnetic behavior between 10 and 400 K. In the partially dehydrated C(n)-4 the spin transition is induced by the change of the aggregate state of matter (solid<-->liquid crystal). For compound C(18)-6 the full dehydration to C(18)-7 provokes the spin-state change of nearly 50% of the Fe(II) ions. The compounds C(n)-3 and C(18)-6 are dark purple in the LS state and become light purple-brown when 50% of the Fe(II) atoms are in the HS state. 相似文献
10.
Olesia I. Kucheriv Dr. Sergii I. Shylin Valerii Y. Sirenko Dr. Vadim Ksenofontov Prof. Wolfgang Tremel Dr. Ioan-Andrei Dascălu Dr. Sergiu Shova Dr. Il'ya A. Gural'skiy 《Chemistry (Weinheim an der Bergstrasse, Germany)》2022,28(44):e202200924
Spin-crossover complexes with multistep transitions attract much attention due to their potential applications as multi-switches and for data storage. A four-step spin crossover is observed in the new iron(II)-based cyanometallic guest-free framework compound Fe(2-ethoxypyrazine)2{Ag(CN)2}2 during the transition from the low-spin to the high-spin state. A reverse process occurs in three steps. Crystallographic studies reveal an associated stepwise evolution of the crystal structures. Multiple transitions in the reported complex originate from distinct FeII sites which exist due to the packing of the ligand with a bulky substituent. 相似文献