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Golovnev, N. N.
Structure of two novel fluoroquinolone salts / N. N. Golovnev, A. D. Vasiliev, A. V. Demina // J. Struct. Chem. - 2021. - Vol. 62, Is. 2. - P. 236-243, DOI 10.1134/S0022476621020074. - Cited References: 23. - The reported study was funded by RFBR, project number 19-52-80003 . - ISSN 0022-4766
Кл.слова (ненормированные):
ciprofloxacinium dichloride -- tetrakis(levofloxacin) tris{hexachlorostannate(IV)} dichloride -- synthesis -- structure -- properties
Аннотация: Fluoroquinolone compounds with the composition CfH2+2, 2Cl–, H2O (CfH2Cl2·H2O (I)) and 4LevoH2+2, 3[SnCl6]2–, 2Cl–, 2H2O ((LevoH2)4[SnCl6]3Cl2·2H2O (II)) (Cf is ciprofloxacin, Levo is levofloxacin) are prepared. Their structures are determined by XRSCD. Crystals I are monoclinic: a = 8.6389(11) Å, b = 14.5486(19) Å, c = 14.8605(19) Å, β = 91.914(3)°, V = 1866.7(4) Å3, space group P21/c, Z = 4. Crystals II are triclinic: a = 12.4821(8) Å, b = 13.8144(8) Å, c = 15.2342(9) Å, α = 84.360(1)°, β = 79.265(1)°, γ = 74.038(1)°, V = 2478.3(3) Å3, space group P1, Z = 1. The structures are stabilized by multiple hydrogen bonds. The photoluminescent properties and thermal stability of compound I are considered.

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Публикация на русском языке Головнев Н. Н. Структура двух новых солей фторхинолонов [Текст] / Н. Н. Головнев, А. Д. Васильев, А. В. Демина // Журн. структ. химии. - 2021. - Т. 62 № 2. - С. 250-257

Держатели документа:
Siberian Federal University, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Vasiliev, A. D.; Васильев, Александр Дмитриевич; Demina, A. V.
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Головнев, Н. Н.
Структура двух новых солей фторхинолонов / Н. Н. Головнев, А. Д. Васильев, А. В. Демина // Журн. структ. химии. - 2021. - Т. 62, № 2. - С. 250-257, DOI 10.26902/JSC_id68338. - Библиогр.: 23. - Исследование выполнено при финансовой поддержке Российского фонда фундаментальных исследований в рамках научного проекта № 19-52-80003 . - ISSN 0136-7463. - ISSN 2542-0976
Кл.слова (ненормированные):
дихлорид ципрофлоксациния -- дихлорид трис{гексахлоростаннат(IV)} тетракис(левофлоксациниума) -- синтез -- структура -- свойства
Аннотация: Синтезированы соединения фторхинолонов состава CfH22+, 2Cl–, H2O (CfH2Cl2·H2O (I)) и 4LevoH22+, 3[SnCl6]2–, 2Cl–, 2H2O ((LevoH2)4[SnCl6]3Cl2·2H2O (II)) (Cf — ципрофлоксацин, Levo — левофлоксацин). Методом РСА определены их структуры. Кристаллы I моноклинные: a = 8.6389(11) Å, b = 14.5486(19) Å, c = 14.8605(19) Å, β = 91.914(3)°, V = 1866.7(4) Å3, пространственная группа P21/c, Z = 4. Кристаллы II триклинные: a = 12.4821(8) Å, b = 13.8144(8) Å, c = 15.2342(9) Å, α = 84.360(1)°, β = 79.265(1)°, γ = 74.038(1)°, V = 2478.3(3) Å3, пространственная группа P1, Z = 1. Структуры стабилизированы многочисленными водородными связями. Рассмотрены фотолюминесцентные свойства и термическая устойчивость соединения I.

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Переводная версия Golovnev N. N. Structure of two novel fluoroquinolone salts [Текст] / N. N. Golovnev, A. D. Vasiliev, A. V. Demina // J. Struct. Chem. - 2021. - Vol. 62 Is. 2.- P.236-243

Держатели документа:
Сибирский федеральный университет, Красноярск, Россия
Институт физики им. Л.В. Киренского СО РАН, Красноярск, Россия

Доп.точки доступа:
Васильев, Александр Дмитриевич; Vasiliev, A. D.; Демина, А. В.
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    Manganese-gold-manganese complex with vinylidene and acetylide units / V. V. Verpekin, A. M. Shor, A. D. Vasiliev [et al.] // Dalton Trans. - 2020. - Vol. 49, Is. 48. - P. 17527-17531, DOI 10.1039/d0dt03530k. - Cited References: 27. - The reported study was funded by Russian Foundation for Basic Research, Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science, in frameworks of the project “New compounds based on gold and noble metals: synthesis, physico-chemical properties, catalytic activity” (grant no. 18-43-240010). This work was conducted within the frame-work of the budget project АААА-А17-117021310221-7 for Institute of Chemistry and Chemical Technology SB RAS using the equipment of Krasnoyarsk Regional Research Equipment Centre of SB RAS. The calculations were carried out at the Siberian Supercomputer Center of the Siberian Branch of the Russian Academy of Sciences (Novosibirsk, Russia). Authors are grateful to Nina I. Pavlenko for IR data, and to Anatoly I. Rubaylo and Nikolai A. Ustynyuk for useful discussions . - ISSN 1477-9226
   Перевод заглавия: Комплекс марганец-золото-марганец с винилиденовыми и ацетилидными блоками
Аннотация: A series of reactions of Cp(CO)2Mn[double bond, length as m-dash]C[double bond, length as m-dash]CHPh with different gold(I) complexes of [Au–C[triple bond, length as m-dash]C–R]n (R = 4-C5H4N, C6H5) and (tht)AuCl yielded one novel trinuclear MnAuMn cluster. The structure of this cluster can be rationalized as being formed of a vinylidene Mn–Au binuclear and Mn–acetylide fragments, and the binding between those is achieved mainly through the sharing of the electron pair of the single Mn–C σ-bond of an acetylide unit with the gold center.

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Держатели документа:
Institute of Chemistry and Chemical Technology SB RAS, Krasnoyarsk Research Center, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50-24, Krasnoyarsk, 660036, Russian Federation
Institute of Physics SB RAS, Krasnoyarsk Research Center, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50-38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Svobodny Prospect 79, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Verpekin, V. V.; Shor, A. M.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Kondrasenko, A. A.; Chudin, O. S.; Ivanova-Shor, E. A.
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    Киселев, Евгений Геннадьевич.
    Синтез и характеристики многокомпонентных ПГА / Е. Г. Киселев, А. Д. Васильев, Т. Г. Волова // Журн. СФУ. Биология. - 2021. - Т. 14, № 1. - С. 97-113 ; J. Sib. Fed. Univ. Biol., DOI 10.17516/1997-1389-0325. - Библиогр.: 32. - Работа выполнена по гранту No 19-43-240012 «Биологические и физические принципы получения биоматериалов новой генерации» при поддержке РФФИ и ККФН и госзаданию Министерства науки и высшего образования РФ No FSRZ-2020-0006. В работе использовано оборудование Центра коллективного пользования приборами ФИЦ «КНЦ СО РАН» . - ISSN 1997-1389. - ISSN 2313-5530
   Перевод заглавия: Synthesis and Characterization of Multicomponent PHAs
Кл.слова (ненормированные):
полигидроксиалканоаты (ПГА) -- биосинтез -- субстраты-предшественники -- сополимеры -- физико-химические свойства -- polyhydroxyalkanoates (PHAs) -- biosynthesis -- precursor substrates -- copolymers -- physicochemical properties
Аннотация: В культуре бактерий Cupriavidus necator B10646 в режиме синтеза резервных полигидроксиалканоатов при включении в состав ростовой среды, помимо основного субстрата, глюкозы, субстратов-предшественников различных мономеров монокарбоновых кислот – солей валериановой и гексановой кислот, пропионата, γ-бутиролактона, синтезировано семейство трех- и четырехкомпонентных полимеров с различным набором и соотношением мономеров и исследованы физико-химические свойства. Трехкомпонентные образцы были образованы мономерами 3-гидроксибутирата (3ГБ), 3-гидроксивалерата (3ГВ), 4-гидроксибутирата (4ГБ) или 3-гидроксигексаноата (3ГГ) и имели следующие составы: П(3ГБ/3ГВ/4ГБ) и П(3ГБ/3ГВ/4ГГ); четырехкомпонентные сополимеры имели состав П(3ГБ/3ГВ/4ГБ/3ГГ). Все сополимерные образцы, независимо от состава и соотношения мономеров, обладали сниженными значениями молекулярной массы и повышенными значениями полидисперсности по сравнению с высококристалличным гомополимером 3-гидроксибутирата, но сохраняли свойства термостабильности, имея разрыв между температурой плавления и термической деградации не менее 100-110 °С. Включение в С-цепь 3ГБ мономеров 3ГВ, 4ГБ и 3ГГ вызывало значительные изменения соотношения кристаллической и аморфной фаз и снижение степени кристалличности (Сх), зависящие от типа мономеров и их содержания в сополимере. Максимальное снижение Сх (до 9-17 %) зарегистрировано у трехкомпонентных образцов П(3ГБ/3ГВ/4ГБ), у четырехкомпонентных сополимеров П(3ГБ/3ГВ/4ГБ/3ГГ) – до 30-36 %. Доказана возможность синтеза полимеров разного, в том числе нового, состава, существенно различающихся базовыми свойствами.
Cupriavidus necator B10646 bacterial cells were cultivated in the mode of synthesis of the reserve polyhydroxyalkanoates (PHAs) in the growth medium that contained, in addition to glucose as the main substrate, precursor substrates of the monomers of various monocarboxylic acids – salts of valeric and hexanoic acids, propionate, and γ-butyrolactone. PHA terpolymers and quaterpolymers with different compositions and proportions of monomers were synthesized, and their physicochemical properties were studied. The terpolymers were composed of monomers of 3-hydroxybutyrate (3HB), 3-hydroxyvalerate (3HV), 4-hydroxybutyrate (4HB), or 3-hydroxyhexanoate (3HHx) and had the following compositions: P(3HB/3HB/4HHx) and P(3HB/3HV/4HHx). The quaterpolymers had the following composition: P(3HB/3HV/4HB/3HHx). All copolymer samples, regardless of the composition and proportions of monomers, had lower molecular weights and higher polydispersity values compared to the highly crystalline 3-hydroxybutyrate homopolymer, but retained thermal stability properties, with a difference between the melting point and thermal degradation of at least 100-110 °С. The inclusion of 3HV, 4HB, and 3HHx monomers in the C-chain of 3HB caused changes in the crystalline to amorphous phase ratio and a significant decrease in the degree of crystallinity (Cx), which depended on the type of monomers and their contents in the copolymer. The maximum decrease in Cx (9-17 %) was detected in the P(3HB/3HV/4HB) terpolymer and the P(3HB/3HV/4HB/3HHx) quaterpolymer (30-36 %). The study confirms that there is the possibility of synthesizing polymers with various compositions, including new ones, which differ significantly in their basic properties.

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Держатели документа:
Институт биофизики СО РАН ФИЦ «Красноярский научный центр СО РАН», Российская Федерация, Красноярск
Сибирский федеральный университет, Российская Федерация, Красноярск
Институт физики им. Л.В. Киренского ФИЦ «Красноярский научный центр СО РАН», Российская Федерация, Красноярск

Доп.точки доступа:
Васильев, Александр Дмитриевич; Vasiliev, A. D.; Волова, Т. Г.

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Properties of degradable polyhydroxyalkanoates (PHAs) synthesized by a new strain, Cupriavidus necator IBP/SFU-1, from various carbon sources / N. O. Zhila, K. Yu. Sapozhnikova, E. G. Kiselev [et al.] // Polymers. - 2021. - Vol. 13, Is. 18. - Ст. 3142, DOI 10.3390/polym13183142. - Cited References: 78. - This work was financially supported by Project “Agropreparations of the new generation: a strategy of construction and realization” (Agreement No 075-15-2021-626) in accordance with Resolution No 220 of the Government of the Russian Federation of 9 April 2010, “On measures designed to attract leading scientists to the Russian institutions of higher learning” (strain isolation, polymer synthesis and investigation), and by the State Assignment of the Ministry of Science and Higher Education of the Russian Federation No. FSRZ-2020-0006 (study of film properties) . - ISSN 2073-4360
Кл.слова (ненормированные):
Cupriavidus necator IBP/SFU-1 -- cell growth and PHA synthesis -- various carbon sources -- PHA composition and properties -- polymer films
Аннотация: The bacterial strain isolated from soil was identified as Cupriavidus necator IBP/SFU-1 and investigated as a PHA producer. The strain was found to be able to grow and synthesize PHAs under autotrophic conditions and showed a broad organotrophic potential towards different carbon sources: sugars, glycerol, fatty acids, and plant oils. The highest cell concentrations (7–8 g/L) and PHA contents were produced from oleic acid (78%), fructose, glucose, and palm oil (over 80%). The type of the carbon source influenced the PHA chemical composition and properties: when grown on oleic acid, the strain synthesized the P(3HB-co-3HV) copolymer; on plant oils, the P(3HB-co-3HV-co-3HHx) terpolymer, and on the other substrates, the P(3HB) homopolymer. The type of the carbon source influenced molecular-weight properties of PHAs: P(3HB) synthesized under autotrophic growth conditions, from CO2, had the highest number-average (290 ± 15 kDa) and weight-average (850 ± 25 kDa) molecular weights and the lowest polydispersity (2.9 ± 0.2); polymers synthesized from organic carbon sources showed increased polydispersity and reduced molecular weight. The carbon source was not found to affect the degree of crystallinity and thermal properties of the PHAs. The type of the carbon source determined not only PHA composition and molecular weight but also surface microstructure and porosity of the polymer films. The new strain can be recommended as a promising P(3HB) producer from palm oil, oleic acid, and sugars (fructose and glucose) and as a producer of P(3HB-co-3HV) from oleic acid and P(3HB-co-3HV-co-3HHx) from palm oil.

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Держатели документа:
Basic Department of Biotechnology, School of Fundamental Biology and Biotechnology, Siberian Federal University, 79 Svobodnyi Av., Krasnoyarsk, 660041, Russian Federation
Federal Research Center, “Krasnoyarsk Science Center SB RAS”, Institute of Biophysics SB RAS, 50/50 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Federal Research Center, “Krasnoyarsk Science Center SB RAS”, L.V. Kirensky Institute of Physics SB RAS, 50/38 Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Federal Research Center, “Krasnoyarsk Science Center of the Siberian Branch of the Russian Academy of Sciences”, 50 Akademgorodok, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Zhila, N. O.; Sapozhnikova, K. Yu.; Kiselev, E. G.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Nemtsev, I. V.; Немцев, Иван Васильевич; Shishatskaya, E. I.; Volova, T. G.
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Structure, UV spectroscopic and electrochemical properties of 2-methyl-8-quinolinolato rhodium (I) complexes, containing carbonyl, triphenylphosphine or triphenylphosphite ligands / V. V. Verpekin, A. D. Vasiliev, N. G. Maksimov [et al.] // J. Mol. Struct. - 2022. - Vol. 1249. - Ст. 131557, DOI 10.1016/j.molstruc.2021.131557. - Cited References: 31. - This work was conducted within the framework of the budget project # 121031500209-6 for Institute of Chemistry and Chemical Technology SB RAS using the equipment of Krasnoyarsk Regional Research Equipment center of Federal Research center, SB RAS. Authors are grateful to Alexander A. Kondrasenko for NMR measurements . - ISSN 0022-2860
Кл.слова (ненормированные):
Rhodium -- 2-methyl-8-quinolinolate -- Carbonyl -- Triphenylphosphine -- Triphenylphosphite -- Electrochemistry -- UV spectroscopy -- X-ray structure
Аннотация: The known Rh(2-Me-8-Oxq)(CO)2 complex (1) was prepared through treatment of dicarbonyl(acetylacetonate)rhodium (I) with 2-methyl-8-hydroxyquinoline for the first time. The reactions of 1 with triphenylphosphine and triphenylphosphite result in complexes Rh(2-Me-8-Oxq)(PPh3)(CO) (2) and Rh(2-Me-8-Oxq)[P(OPh)3](CO) (3) that were characterized by IR and NMR spectroscopy. The structures of complexes 2 and 3 were determined by single-crystal X-ray diffraction analysis. The complexes show the 2-methyl-8-quinolinolato ligand in the expected coordination mode with a slightly disordered square planar geometry at the rhodium center. In the crystal, molecules of Rh(2-Ме-8-Oxq)(CO)(PPh3) (2) form centrosymmetric dimers due to π-stacking interactions. No intermolecular contacts are observed in the crystal of 3. The UV spectroscopic and electrochemical properties of complexes 1–3 were studied. Their electronic spectra in CH3CN show three quinoline-centered absorptions. The electrochemical study revealed that the oxidation of the complexes 1–3 is two-electron and leads to the formation of dication Rh (III) species while their reduction gives radical anions, which undergoes rapid decomposition.

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Держатели документа:
Institute of Chemistry and Chemical Technology SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-24, Krasnoyarsk, 660036, Russian Federation
Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-38, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Svobodny Prospect, 79, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Verpekin, V. V.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Maksimov, N. G.; Burmakina, G. V.; Zimonin, D. V.; Nedelina, T. S.; Chudin, O. S.; Rubaylo, A. I.
}
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Co5/3Nb1/3BO4: A new cobalt oxyborate with a complex magnetic structure / N. V. Kazak, N. A. Belskaya, E. M. Moshkina [et al.] // J. Magn. Magn. Mater. - 2021. - Vol. 534. - Ст. 168056, DOI 10.1016/j.jmmm.2021.168056. - Cited References: 50. - The authors acknowledge M. Molokeev for the orientating the single crystal for magnetic measurements. The X-ray diffraction and specific heat measurements were carried out in the Common Access Facility Centres of SB RAS (Krasnoyarsk, Russia) and P.N. Lebedev Physical Institute of RAS (Moscow, Russia). This work has been financed by the Russian Foundation for Basic Research (project no. 20-02-00559). We acknowledge financial support from the Spanish MINECO DWARFS project MAT2017-83468-R and Gobierno de Aragón (Group, E12-20R) . - ISSN 0304-8853
Кл.слова (ненормированные):
Warwickites -- Ferrimagnet
Аннотация: Needle-shape single crystals of Co5/3Nb1/3BO4 warwickite were grown using the flux technique. X-ray diffraction measurements have revealed an orthorhombic structure (Sp. Gr. Pbnm) where the octahedral M1 site is occupied by a mixture of Co2+/Nb5+ ions and the M2 site is exclusively filled by Co2+ ions. Using dc magnetization measurements it was established that the new material undergoes two magnetic transitions: an antiferromagnetic transition at TN1 = 27 K and a ferrimagnetic one at TN2 = 14 K, below which a hysteresis cycle opens. Both magnetic transitions are marked by anomalies in the specific heat. High magnetic anisotropy with c-axis as a hard magnetization direction was detected.

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Держатели документа:
Kirensky Institute of Physics, FRC SB RAS, Krasnoyarsk, Russian Federation
Reshetnev Siberian State University of Science and Technology, Krasnoyarsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation
Instituto de Nanociencia y Materiales de Aragon (INMA), CSIC-Universidad de Zaragoza and Departamento de Fisica de la Materia Condensada, Zaragoza, 50009, Spain
Servicio de Medidas Fisicas, Universidad de Zaragoza, Zaragoza, Spain
P.N. Lebedev, Physical Institute of RAS, Moscow, 119991, Russian Federation

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Belskaya, N. A.; Moshkina, E. M.; Мошкина, Евгения Михайловна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Bartolome, J.; Arauzo, A.; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Gavrilkin, S. Y.; Gorev, M. V.; Горев, Михаил Васильевич; Patrin, G. S.; Патрин, Геннадий Семёнович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
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    Comparative study of the magnetic phase diagrams and spin-flop-driven magnetodielectric responses of the pure and Mn3+-doped Pb2Fe2Ge2O9 single crystals / A. Pankrats, M. Kolkov, A. Balaev [et al.] // J. Magn. Magn. Mater. - 2021. - Vol. 534. - Ст. 168023, DOI 10.1016/j.jmmm.2021.168023. - Cited References: 21. - This study was supported by the Russian Foundation for Basic Research, the Government of the Krasnoyarsk Territory, and the Krasnoyarsk Territorial Foundation for Support of Scientific and R&D Activities, project no. 18-42-240008 “Effect of the Magnetic Structure on the Magnetodielectric Properties of Oxide Crystals Containing Stereoactive Pb 2+ and Bi 3+ Ions” . - ISSN 0304-8853
   Перевод заглавия: Сравнительное исследование магнитных фазовых диаграмм и индуцированных спин-флоп переходом магнитодиэлектрических откликов в чистом и допированном Mn3+ монокристаллах Pb2Fe2Ge2O9
Кл.слова (ненормированные):
Magnetic structure -- Magnetic anisotropy -- Magnetodielectric properties -- Spin reorientation -- Magnetic phase diagram
Аннотация: The Pb2Fe2-xMnxGe2O9 (x = 0.43) orthorhombic antiferromagnet single crystals have been synthesized by a modified pseudo-flux technique and their magnetic and magnetodielectric properties have been investigated. It has been established that partial substitution of highly anisotropic Mn3+ ions for iron ones significantly affects the magnetic structure of the crystal. Under magnetization of the crystal along the rhombic b and c axes, magnetization jumps have been detected, which are indicative of the occurrence of orientational transitions identified as first-order ones. No weak ferromagnetism characteristic of the pure crystal in the rhombic a axis direction has been detected. The field dependences of the magnetization for the pure and Mn-doped crystals have been analyzed using the thermodynamic potential that takes into account the crystal symmetry. It has been shown that, in the Mn-substituted crystal, the antiferromagnetic vector in the ground state is parallel to the rhombic b axis; in this state, weak ferromagnetism has not been observed. Under magnetization along the b axis, a conventional spin-flop transition occurs. The orientational transition under magnetization along the c axis has been attributed to the reorientation of the antiferromagnetic vector relative to the a axis with the simultaneous occurrence of a weak ferromagnetic moment along the c axis. Magnetic phase diagrams of the Mn-doped crystal for the magnetic fields H||b and H||c have been built. In the Mn-doped crystal, at E||c and H||c, the orientational transition-induced magnetodielectric response jump has been detected, which is higher than the jumps observed for the undoped crystal by a factor of 3. The magnetodielectric properties of the pure and Mn-doped crystals have been analyzed using their magnetic phase diagrams.

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Держатели документа:
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, 660036, Russian Federation
Siberian Federal University, Krasnoyarsk, 660041, Russian Federation

Доп.точки доступа:
Pankrats, A. I.; Панкрац, Анатолий Иванович; Kolkov, M. I.; Колков, Максим Игоревич; Balaev, A. D.; Балаев, Александр Дмитриевич; Freydman, A. L.; Фрейдман, Александр Леонидович; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Balaev, D. A.; Балаев, Дмитрий Александрович
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Antiferromagnetism of the cation-ordered warwickite system Mn2-xMgxBO4 (x=0.5, 0.6 and 0.7) / N. V. Kazak, N. A. Belskaya, E. M. Moshkina [et al.] // J. Magn. Magn. Mater. - 2020. - Vol. 507. - Ст. 166820, DOI 10.1016/j.jmmm.2020.166820. - Cited References: 39. - The reported study was funded by the Russian Foundation for Basic Research (no. 20-02-00559), Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science to the research project. 18-42243007. . - ISSN 0304-8853. - ISSN 1873-4766

РУБ Materials Science, Multidisciplinary + Physics, Condensed Matter
Рубрики:
SPIN-GLASS BEHAVIOR
   CRYSTAL-STRUCTURES
   SINGLE-CRYSTALS
   INSIGHTS
   MGFEBO4
Кл.слова (ненормированные):
Warwickites -- Antiferromagnet -- Cation ordering -- Jahn-Teller distortions
Аннотация: X-ray diffraction, heat capacity and magnetic measurements are performed on single crystals of Mn2-xMgxBO4 (x = 0.5, 0.6 and 0.7) with the warwickite structure. The monoclinic symmetry is found for all samples with the space group P21/n. The M1 site is occupied by trivalent Mn ions while the M2 site is occupied by a mixture of divalent Mg and Mn ions. Regular cation and charge distributions are observed, which is unusual for heterometallic warwickites. The local octahedral distortions of M1O6 show the monotonic dependence on the Mg content and are in accordance with the Jahn-Teller distortion. All samples are found to undergo long-range antiferromagnetic ordering with rather low transition temperatures of TN = 16, 14 and 13 K for x = 0.5, 0.6, and 0.7, respectively. The ordering of local octahedral distortions, caused by the strong electron-phonon interaction of the trivalent Mn ions, is proposed to stabilise the cationic ordering and, as a result, the long-range magnetic ordering in the material.

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Держатели документа:
FRC SB RAS, Kirensky Inst Phys, Krasnoyarsk, Russia.
Reshetnev Siberian State Univ Sci & Technol, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.
RAS, Zavoisky Phys Tech Inst, FRC Kazan Sci Ctr, Kazan, Russia.
Kazan Volga Reg Fed Univ, Kazan, Russia.

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Belskaya, N. A.; Moshkina, E. M.; Мошкина, Евгения Михайловна; Bezmaternykh, L. N.; Безматерных, Леонард Николаевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Sofronova, S. N.; Софронова, Светлана Николаевна; Eremina, R. M.; Eremin, E. V.; Еремин, Евгений Владимирович; Muftakhutdinov, A. R.; Cherosov, M. A.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [20-02-00559]; Government of Krasnoyarsk Territory; Krasnoyarsk Regional Fund of Science to the research project [18-42243007]
}
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10.

Catalyzed M–C coupling reactions in the synthesis of σ-(pyridylethynyl)dicarbonylcyclopentadienyliron complexes / V. V. Verpekin, O. V. Semeikin, A. D. Vasiliev [et al.] // RSC Adv. - 2020. - Vol. 10, Is. 29. - P. 17014-17025, DOI 10.1039/d0ra02333g. - Cited References: 86. - This research was funded by a grant from the Russian Science Foundation (project No. 18-73-00150). . - ISSN 2046-2069

РУБ Chemistry, Multidisciplinary
Рубрики:
NONLINEAR-OPTICAL PROPERTIES
METAL ALKYNYL COMPLEXES
CARBON BOND FORMATION
Аннотация: The reactions between terminal ethynylpyridines, (trimethylsilyl)ethynylpyridines and cyclopentadienyliron dicarbonyl iodide were studied under Pd/Cu-catalyzed conditions to develop a synthetic approach to the σ-alkynyl iron complexes Cp(CO)2Fe–C≡C–R (R = ortho-, meta-, para-pyridyl). Depending on the catalyst and reagents used, the yields of the desired σ-pyridylethynyl complexes varied from 40 to 95%. In some cases the reactions with ortho-ethynylpyridine gave as byproduct the unexpected binuclear FePd μ-pyridylvinylidene complex [Cp(CO)Fe{μ2-η1(Cα):η1(Cα)-κ1(N)-Cα=Cβ(H)(o-C5H4N)}(μ-CO)PdI]. The conditions, catalysts, and reagents that provide the highest yields of the desired σ-pyridylethynyl iron compounds were determined. The methods developed allowed the synthesis of the corresponding σ-4-benzothiadiazolylethynyl complex Cp(CO)2Fe–C≡C–(4-C6H3N2S) as well. Eventually, synthetic approaches to σ-alkynyl iron complexes of the type Cp(CO)2Fe–C≡C–R (R = ortho-, meta-, para-pyridyl, 4-benzothiadiazol-2,1,3-yl) based on the Pd/Cu-catalyzed cross-coupling reactions were elaborated.

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Держатели документа:
Russian Acad Sci, Krasnoyarsk Res Ctr, Siberian Branch, Inst Chem & Chem Technol, Akademgorodok 50-24, Krasnoyarsk 660036, Russia.
Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Ul Vavilova 28, Moscow 119991, Russia.
Russian Acad Sci, Siberian Branch, Krasnoyarsk Res Ctr, Inst Phys, Akademgorodok 50-38, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sobodny Prospect 79, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Verpekin, Victor V.; Semeikin, Oleg, V; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Kondrasenko, Alexander A.; Belousov, Yu. A.; Ustynyuk, Nikolai A.; Russian Science FoundationRussian Science Foundation (RSF) [18-73-00150]
}
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