Библиотека института физики им. Л.В. Киренского СО РАН

Главная

Базы данных

Труды сотрудников ИФ СО РАН - результаты поиска

Вид поиска

Каталог книг и брошюр библиотеки ИФ СО РАН

Каталог журналов библиотеки ИФ СО РАН

Труды сотрудников ИФ СО РАН

Область поиска

в найденном

Найдено в других БД:

Каталог книг и брошюр библиотеки ИФ СО РАН (3)

Каталог журналов библиотеки ИФ СО РАН (2)

Формат представления найденных документов:
полный	информационный	краткий

Отсортировать найденные документы по:
автору	заглавию	году издания	типу документа

Поисковый запрос: (<.>K=Spectrometry<.>)

Общее количество найденных документов : 6
Показаны документы с 1 по 6

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Vtyurin A. N., Bulou A., Krylov A. S., Shmygol I. V., Aleksandrov K. S.
Заглавие : Raman scattering study of the upper phase transition in CsScF4
Место публикации : Journal of Raman Spectroscopy. - 2000. - Vol. 31, Is. 3. - P.151-155. - ISSN 0377-0486, DOI 10.1002/(SICI)1097-4555(200003)31:3151::AID-JRS5103.0.CO;2-T
Ключевые слова (''Своб.индексиров.''): article--crystal--heating--high temperature--melting point--neutron scattering--phase transition--photon--raman spectrometry--temperature dependence
Аннотация: Effects of the phase transition between the high-temperature tetragonal phases of the CsScF4 crystal were studied by Raman scattering. The appearance of new lines including a soft mode was observed below the phase transition point, in complete accordance with the new crystal symmetry. The behavior of the soft mode, which corresponds to in-phase rotations of ScF6 rigid groups around the z-axis (and out-of-phase within perovskite-like layers), resembles that observed earlier in RbAlF4, which suggests a similar mechanism of this transition in both crystals. Copyright (C) 2000 John Wiley and Sons, Ltd.
Scopus,
Читать в сети ИФ
Найти похожие

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Atuchin V. V., Beisel N. F., Galashov E. N., Mandrik E. M., Molokeev M. S., Yelisseyev A. P., Yusuf A. A., Xia Z.
Заглавие : Pressure-stimulated synthesis and luminescence properties of microcrystalline (Lu,Y)3Al5O12:Ce3+ garnet phosphors
Место публикации : ACS Appl. Mater. Interfaces: American Chemical Society, 2015. - Vol. 7, Is. 47. - P.26235-26243. - ISSN 19448244 (ISSN), DOI 10.1021/acsami.5b08411
Примечания : Cited References: 75. - This work was partly supported by the National Natural Science Foundations of China (Grant Nos. 51272242 and 51511130035) and the Russian Foundation for Basic Research (Grant No. 15-52-53080 GFEN_a). V.V.A. was partly supported by the Ministry of Education and Science of the Russian Federation
Предметные рубрики: LASER MASS-SPECTROMETRY
LIGHT-EMITTING-DIODES
WHITE-LIGHT
SINGLE-CRYSTALS
OPTICAL-PROPERTIES
ELECTRONIC-STRUCTURE
VIBRATIONAL PROPERTIES
PHASE-TRANSITIONS
PARTICLE-SIZE
GROWTH
Ключевые слова (''Своб.индексиров.''): synthesis--pressure--garnet--structure--luminescence--phosphor
Аннотация: The Lu2.98Ce0.01Y0.01Al5O12 and Y2.99Ce0.01Al5O12 phosphors were synthesized by solid state reaction at temperature 1623 K and pressure 1.5 × 107 Pa in (95% N2 + 5% H2) atmosphere. Under the conditions, the compounds crystallize in the form of isolated euhedral partly faceted microcrystals ∼19 μm in size. The crystal structures of the Lu2.98Ce0.01Y0.01Al5O12 and Y2.99Ce0.01Al5O12 garnets have been obtained by Rietveld analysis. The photoluminescence (PL) and X-ray excited luminescence (XL) spectra obtained at room temperature indicate broad asymmetric bands with maxima near 519 and 540 nm for Y2.99Ce0.01Al5O12 and Lu2.98Ce0.01Y0.01Al5O12, respectively. The light source was fabricated using the powder Lu2.98Ce0.01Y0.01Al5O12 phosphor and commercial blue-emitting n-UV LED chips (λex = 450 nm). It is found that the CIE chromaticity coordinates are (x = 0.388, y = 0.563) with the warm white light emission correlated color temperature (CCT) of 6400 K and good luminous efficiency of 110 lm/W. © 2015 American Chemical Society.
Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Найти похожие

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Golovnev N. N., Molokeev M. S., Sterkhova I. V., Goryunov Y. V., Atuchin V. V.
Заглавие : New class of bicyclic compounds derived from thiobarbituric acid with representative compound 1,3-diethyl-7-hydroxy-5,5,7-trimethyl-2-thioxo-1,2,3,5,6,7-hexahydro-4H-pyrano[2,3-d]pyrimidin-4-one. Preparation, crystal structure, mass spectrometry and IR spectroscopy
Место публикации : J. Mol. Struct.: Elsevier, 2015. - Vol. 1102. - P.101-107. - ISSN 0022-2860, DOI 10.1016/j.molstruc.2015.08.046
Примечания : Cited References: 40. - The work was carried out within the public task of the Ministry of Education and Science of the Russian Federation for research engineering of the Siberian Federal University in 2015 (Contract 3049). V.V.A. is grateful to the Ministry of Education and Science of the Russian Federation for the financial support of the investigation (Contract 14.607.21.0106). The authors also thank SFU CEJU for the technical support
Предметные рубрики: 1,3-diethyl-2-thiobarbituric acid
Crystal-structure
2-thiobarbituric acid
Barbituric-acid
Hydrogen-bond
Derivatives
Diffraction
Equilibria
Inhibitors
Series
Ключевые слова (''Своб.индексиров.''): bicyclic compounds--thiobarbiturates--heterocycles--x-ray diffraction--ir spectroscopy--theoretical calculations
Аннотация: The colorless crystals of 1,3-diethyl-7-hydroxy-5,5,7-trimethyl-2-thioxo-1,2,3,5,6,7-hexahydro-4H-pyrano[2,3-d]pyrimidin-4-one (1) have been crystallized from the solution containing 1,3-diethyl-2-thiobarbituric acid (HDETBA) and equal volumes of concentrated HCl and acetone A possible stoichiometric reaction mechanism has been suggested. The crystal structure of 1 has been determined by X-ray single crystal analysis. The phase purity of the precipitate has been verified by powder X-ray diffraction analysis. Compound 1 crystallizes in the orthorhombic structure, space group P212121, with cell parameters a = 9.7454(4), b = 11.2225(4), c = 13.9171(5) Å, Z = 4, V = 1522.1(1) Å3. The molecules of 1 contain the bicyclic ring constructions new in thiobarbiturates. The molecules of 1 are linked by O-H...O hydrogen bonds to infinite molecule chains. The results of mass spectrometric analysis, theoretical studies and IR spectroscopy confirm the structure of 1. Using the PASS software, the general pharmacological potential of 1 was analyzed.
Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Найти похожие

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Lupu, Loredana, Wiegand, Pascal, Huttmann N., Rawer, Stephan, Kleinekofort, Wolfgang, Shugureva, Irina, Kichkailo, Anna S., Tomilin F. N., Lazarev, Alexander, Berezovski, Maxim V., Przybylski, Michael
Заглавие : Molecular epitope determination of aptamer complexes of the multidomain protein C-met by proteolytic affinity-mass spectrometry
Коллективы : LOEWE-3 Funding Agency, Hessen-Agentur, Wiesbaden, Germany [696/19-16]
Место публикации : ChemMedChem. - 2020. - Vol. 15, Is. 4. - P.363-369. - ISSN 1860-7179, DOI 10.1002/cmdc.201900489. - ISSN 1860-7187(eISSN)
Примечания : Cited References: 40. - We gratefully acknowledge the advice and assistance of Prof. Friedemann Volklein and Oliver Muller, MSc in the preparation of chips for the SPR affinity determinations. We thank Dr. Stefan Maeser, Biogen GmbH, Munchen, for valuable advice and critical reading of the manuscript. This work has been partially funded (Chip-MS epitope analysis) by the LOEWE-3 Funding Agency, Hessen-Agentur, Wiesbaden, Germany; Grant 696/19-16
Предметные рубрики: DNA APTAMERS
ANTIBODIES
RECOGNITION
Аннотация: C‐Met protein is a glycosylated receptor tyrosine kinase of the hepatocyte growth factor (HGF), composed of an α and a β chain. Upon ligand binding, C‐Met transmits intracellular signals by a unique multi‐substrate docking site. C‐Met can be aberrantly activated leading to tumorigenesis and other diseases, and has been recognized as a biomarker in cancer diagnosis. C‐Met aptamers have been recently considered a useful tool for detection of cancer biomarkers. Herein we report a molecular interaction study of human C‐Met expressed in kidney cells with two DNA aptamers of 60 and 64 bases (CLN0003 and CLN0004), obtained using the SELEX (Systematic Evolution of Ligands by Exponential Enrichment) procedure. Epitope peptides of aptamer‐C‐Met complexes were identified by proteolytic affinity‐mass spectrometry in combination with SPR biosensor analysis (PROTEX‐SPR‐MS), using high‐pressure proteolysis for efficient digestion. High affinities (KD, 80–510 nM) were determined for aptamer‐C‐Met complexes, with two‐step binding suggested by kinetic analysis. A linear epitope, C‐Met (381–393) was identified for CLN0004, while the CLN0003 aptamer revealed an assembled epitope comprised of two peptide sequences, C‐Met (524–543) and C‐Met (557–568). Structure modeling of C‐Met‐aptamers were consistent with the identified epitopes. Specificities and affinities were ascertained by SPR analysis of the synthetic epitope peptides. The high affinities of aptamers to C‐Met, and the specific epitopes revealed render them of high interest for cellular diagnostic studies.
Смотреть статью,
Scopus,
WOS,
Читать в сети ИФ
Найти похожие

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Habibullayev N. N., Naumov N. G., Lavrov A.N., Kuratieva N. V., Aleksandrovsky A. S., Oreshonkov A. S., Molokeev M. S., Palamarchuk I. V., Yurev I. O., Denisenko Y. G., Andreev O. V., Zakharova A. D.
Заглавие : Magnetic, optical, and thermic properties of SrLnCuSe3 (Ln = Dy, Ho, Er, Tm) compounds
Место публикации : Magnetochemistry. - 2023. - Vol. 9, Is. 8. - Ст.194. - ISSN 23127481 (eISSN), DOI 10.3390/magnetochemistry9080194
Примечания : Cited References: 36. - The study was funded by the Russian Science Foundation, project No. 23-23-00488
Аннотация: SrLnCuSe3 (Ln = Dy, Ho, Er, Tm) compounds crystallize in the Pnma and Cmcm orthorhombic space group and belong to the Eu2CuS3 and KCuZrS3 structural type, respectively. According to a single-crystal XRD study, the SrTmCuSe3 unit cell parameters are a = 4.0631 (4), b = 13.4544 (14), c = 10.4430 (10) A, and V = 570.88 (10) A3. All the studied SrLnCuSe3 samples in the temperature range of 1.77–300 K demonstrate paramagnetic behavior without any features pointing to magnetic ordering. The measured Curie constants coincide with the values expected for Ln3+ ions with good accuracy, which confirms the stoichiometric composition of the samples and the non-magnetic state of the copper ions, Cu1+ (S = 0). The conducted optical absorption study showed that the polycrystalline SrLnCuSe3 (Ln = Dy, Ho, Er, Tm) samples are semiconductors with a direct bandgap ranging from 2.14 eV to 2.31 eV. Two indirect bandgaps were revealed and explained by the presence of optical transitions to highly dispersive subbands in the conduction band. The compounds demonstrate two reversible phase transitions α⇆β, β⇆γ and an incongruent melting at 1606 K (Dy), 1584 K (Ho), 1634 K (Er), and 1620 K (Tm) associated with the formation of solid solutions of SrSe, Cu2-XSe, and Ln2Se3 binary compounds.
смотреть статью,
Scopus,
WOS
Найти похожие

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Mamalis A. G., Ovchinnikov S. G., Petrov M. I., Balaev D. A., Shaihutdinov K. A., Gohfeld D. M., Kharlamova S. A., Vottea I. N.
Заглавие : Composite materials on high-T-c superconductors and BaPbO3, Ag basis
Коллективы : International Conference on New Theories, Discoveries and Applications of Superconductors and Related Materials
Разночтения заглавия :авие SCOPUS: Composite materials on high-Tc superconductors and BaPbO3, Ag basis
Место публикации : Physica C. - 2001. - Vol. 364. - P.174-177. - ISSN 0921-4534, DOI 10.1016/S0921-4534(01)00749-3
Примечания : Cited References: 9
Ключевые слова (''Своб.индексиров.''): composite high-t-c superconductors--superconducting fault current limiter--composite high-tc superconductors--superconducting fault current limiter--composite materials--electric fault currents--interfaces (materials)--magnetic variables measurement--mathematical models--scanning electron microscopy--spectrometry--superconducting transition temperature--superconductivity--x ray diffraction analysis--solid state reactions--high temperature superconductors
Аннотация: The preparation., processing and characterization of the composite materials on high-T-c superconductor (HTSC) basis, YBa2Cu3O7/Ag and Y0.75Lu0.25Ba2Cu3O7/BaPbO3, is reported. The initial components YBa2Cu3O7 and BaPbO3 were prepared by the standard solid state reaction technique. The microstructures of the samples were observed by scanning electron microscopy. whilst the XRD paterns of the composites HTSC+Ag and HTSC+BaPbO3 revealed the 123 superconducting phase and the Ag or BaPbO3 structure. The chemical compositions of the powders and the interface zone were found by employing energy dispersive spectrometry. The resistive and magnetic measurements of the composites indicated the transition temperature 93.5 K. Application of such composite materials in the construction of a superconducting fault current limiter model is reported. (C) 2001 Elsevier Science B.V. All rights reserved.
WOS,
Scopus,
Читать в сети ИФ
Найти похожие