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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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11.

Vasiliev, A. D.
Crystal Structure of Three Ionic Compounds of Levofloxacin / A. D. Vasiliev, N. N. Golovnev // J. Struct. Chem. - 2019. - Vol. 60, Is. 12. - P. 1959-1964, DOI 10.1134/S0022476619120114. - Cited References: 13. - The work was performed within the State Task of the Ministry of Education and Science of the Russian Federation to the Siberian Federal University for 2017-2019 (4.7666.2017/BCh) . - ISSN 0022-4766
Кл.слова (ненормированные):
double charged levofloxacinium cation -- tetrahalides of d-elements -- ionic compounds -- structure
Аннотация: The structures of three ionic compounds of levofloxacin (LevoH or Ci18H20FN3O4) − LevoH3[CoCl4]-H2O (I), LevoH3[ZnBr4]·H2O (II), LevoH3[CuBr4]-H2O·(III) are determined. The crystals of I-III are monoclinic; in compound III, the particles are packed so that the direction of the screw axis does not coincide with the largest unit cell parameter. The asymmetric unit of the unit cell contains two LevoH32+ and CoCl42− ions and two crystallization water molecules in I; two LevoH32+ and MBr42− (M = Cu, Zn) ions and two crystallization water molecules in II and III. The absolute structure of the crystals and the configuration of the chiral center of the levofloxacinium cation S are determined. The structures are stabilized by multiple hydrogen bonds, X−Y π and π-π interactions.

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Публикация на русском языке Васильев, Александр Дмитриевич. Кристаллическая структура трёх ионных соединений левофлоксацина [Текст] / А. Д. Васильев, Н. Н. Головнёв // Журн. структ. химии. - 2019. - Т. 60 № 12. - С. 2044-2049

Держатели документа:
Siberian Federal University, Krasnoyarsk, Russian Federation
Kirensky Institute of Physics, Federal Research Center, Krasnoyarsk Science Center, Siberian Branch, Russian Academy of Sciences, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Golovnev, N. N.; Васильев, Александр Дмитриевич
}
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12.

Chemistry of vinylidene complexes. XXV. Synthesis and reactions of binuclear µ-vinylidene RePt complexes containing phosphite ligands. Spectroscopic, structural and electrochemical study / O. S. Chudin, V. V. Verpekin, A. A. Kondrasenko [et al.] // Inorg. Chim. Acta. - 2020. - Vol. 505. - Ст. 119463, DOI 10.1016/j.ica.2020.119463. - Cited References: 56. - This work was conducted within the framework of the budget project AAAA-A17-117021310221-7 for Institute of Chemistry and Chemical Technology SB RAS using the equipment of Krasnoyarsk Regional Research Equipment Centre of SB RAS . - ISSN 0020-1693
Кл.слова (ненормированные):
Vinylidene complexes -- Rhenium -- Platinum -- NMR -- X-ray diffraction -- Redox properties
Аннотация: Reactions of Cp(CO)2ReCCHPh with Pt[P(OR)3]4 (R = Pri, Et, Ph) gave binuclear μ-vinylidene complexes Cp(CO)2RePt(μ-CCHPh)[P(OR)3]2. Treatment of the previously synthesized Cp(CO)2Re(μ-CCHPh)Pt(PPh3)2 with triisopropylphosphite or triethylphosphite resulted in a stepwise substitution of PPh3 ligands, leading to the disubstituted Cp(CO)2RePt(μ-CCHPh)[P(OR)3]2 and monosubstituted Cp(CO)2RePt(μ-CCHPh)[P(OR)3](PPh3) (R = Pri or Et) species, while no triphenylphosphine ligand substitution in the reaction with P(OPh)3 occurs at all. The monosubstituted Cp(CO)2RePt(μ-CCHPh)[P(OR)3](PPh3) (R = Pri, Et, Ph) species were also obtained by reacting Cp(CO)2ReCCHPh with mixed-ligand complexes Pt(PPh3)3L (L = P(OPri)3, P(OEt)3, P(OPh)3). Reactions of Cp(CO)2RePt(μ-CCHPh)LL′ (L = L′ = P(OPri)3, P(OEt)3, P(OPh)3; L = P(OPri)3, P(OEt)3, P(OPh)3, L′ = PPh3) with Co2(CO)9 yield tricarbonyl vinylidene species Cp(CO)2RePt(μ-CCHPh)[P(OR)3](CO) (R = Pri, Et, Ph). The obtained compounds were characterized by IR and 1H, 13C, 31P NMR spectroscopy. The molecular structures of Cp(CO)2RePt(μ-CCHPh)[P(OPri)3]2, Cp(CO)2RePt(μ-CCHPh)[P(OPri)3](PPh3) and Cp(CO)2RePt(μ-CCHPh)[P(OPri)3](CO) were determined by X-ray diffraction study. The redox properties of the new complexes and their reactions of chemical oxidation were studied.

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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
Siberian Federal University, Svobodny Prospect, 79, Krasnoyarsk, 660041, Russian Federation
Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences, Acad. Lavrentiev Ave., 3, Novosibirsk, 630090, Russian Federation
Novosibirsk State University, 2 Pirogova Str., Novosibirsk, 630090, Russian Federation
Institute of Physics SB RAS, Federal Research Center “Krasnoyarsk Science Center SB RAS”, Akademgorodok, 50-38, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Chudin, O. S.; Verpekin, V. V.; Kondrasenko, A. A.; Burmakina, G. V.; Piryazev, D. A.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Pavlenko, N. I.; Zimonin, D. V.; Rubaylo, A. I.
}
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13.

Forming High-Temperature Superconducting Layers at the Interfaces between Nonsuperconducting Phases / M. I. Petrov, S. I. Popkov, K. Y. Terent’ev, A. D. Vasil’ev // Tech. Phys. Lett. - 2020. - Vol. 46, Is. 10. - P. 1004-1007, DOI 10.1134/S1063785020100247. - Cited References: 14. - The authors are grateful to D.M. Gokhfeld for comments made during the discussion of the results. The results were obtained using a Bruker D8Advance diffractometer (Bruker AXS) and the Quantum Design PPMS vibrating sample magnetometer of the Krasnoyarsk Regional Center for Collective Use, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences . - ISSN 1063-7850
Кл.слова (ненормированные):
high-temperature superconductor -- green phase -- superconducting layer
Аннотация: An alternative technique for synthesizing high-temperature superconductor samples is proposed, in which superconducting layers should form on the surface of hard-melting Ho2BaCuO5 green phase grains immersed in the liquid phase BaCuO2 + CuO.

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Публикация на русском языке Формирование высокотемпературных сверхпроводящих слоев на границах несверхпроводящих фаз [Текст] / М. И. Петров, С. И. Попков, К. Ю. Терентьев, А. Д. Васильев // Письма в Журн. техн. физ. - 2020. - Т. 46 Вып. 20. - С. 11-14

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

Доп.точки доступа:
Petrov, M. I.; Петров, Михаил Иванович; Popkov, S. I.; Попков, Сергей Иванович; Terent'ev, K. Yu.; Терентьев, Константин Юрьевич; Vasil'ev, A. D.; Васильев, Александр Дмитриевич
}
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14.

Формирование высокотемпературных сверхпроводящих слоев на границах несверхпроводящих фаз / М. И. Петров, С. И. Попков, К. Ю. Терентьев, А. Д. Васильев // Письма в Журн. техн. физ. - 2020. - Т. 46, Вып. 20. - С. 11-14, DOI 10.21883/PJTF.2020.20.50148.18289. - Библиогр.: 14. - Результаты получены с использованием оборудования Красноярского регионального центра коллективного пользования ФИЦ КНЦ СО РАН: дифрактометра Bruker D8Advance (Bruker AXS) и вибрационного магнитометра установки PPMS (Quantum Design). Авторы благодарят Д.М. Гохфельда за замечания при обсуждении результатов . - ISSN 0320-0116
Кл.слова (ненормированные):
ВТСП -- зеленая фаза -- сверхпроводящий слой
Аннотация: Предложен альтернативный способ синтеза образцов высокотемпературных сверхпроводников, при котором сверхпроводящие слои должны образовываться на поверхности тугоплавких гранул "зеленой фазы" Ho2BaCuO5, погруженных в жидкую фазу BaCuO2 + CuO.

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Переводная версия Forming High-Temperature Superconducting Layers at the Interfaces between Nonsuperconducting Phases [Текст] / M. I. Petrov, S. I. Popkov, K. Y. Terent’ev, A. D. Vasil’ev // Tech. Phys. Lett. - 2020. - Vol. 46 Is. 10.- P.1004-1007

Держатели документа:
Институт физики им. Л.В. Киренского Сибирского отделения Российской академии наук, Красноярск, Россия
Сибирский федеральный университет, Красноярск, Россия

Доп.точки доступа:
Петров, Михаил Иванович; Petrov, M. I.; Попков, Сергей Иванович; Popkov, S. I.; Терентьев, Константин Юрьевич; Terent'ev, K. Yu.; Васильев, Александр Дмитриевич; Vasil'ev, A. D.
}
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15.

Transition metal catalyzed Fe–C coupling reactions in synthesis of dicarbonyl(2-thienylethynyl)(η5-cyclopentadienyl)iron complex: Spectroscopic, structure and electrochemical study / V. V. Verpekin, I. S. Ahremchik, A. D. Vasiliev [et al.] // Transit. Met. Chem. - 2020. - Vol. 45. - P. 589-594, DOI 10.1007/s11243-020-00413-9. - Cited References: 31. - This research was funded by a grant from the Russian Science Foundation (Project No. 18-73-00150) . - ISSN 0340-4285
Кл.слова (ненормированные):
Catalysis -- Catalysts -- Nuclear magnetic resonance spectroscopy -- Transition metals -- X ray powder diffraction
Аннотация: The new σ-alkynyl iron(II) complex Cp(CO)2Fe-C≡C-(2-C4H3S) was synthesized with application of several known approaches based on the transition metal (Pd/Cu–, Au–, Cu– and Pd–) catalyzed Fe–C coupling reactions of 2-ethynylthiophene or 2-[(trimethylsilyl)ethynyl]thiophene with cyclopentadienyliron dicarbonyl iodide. The yield of the complex in these reactions was found to strongly depend on the catalyst used. The conditions, catalysts, and reagents that provide the highest yields of the desired 2-thienylethynyl iron complex were determined. The complex was characterized by IR, 1H and 13C NMR spectroscopy. The molecular structure of Cp(CO)2Fe–C≡C-(2-C4H3S) established by X-ray diffraction analysis exhibits a three-leg piano stool geometry. The redox properties of the new complex were studied.

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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 prospekt, 79, Krasnoyarsk, 660041, Russian Federation
A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, ul. Vavilova 28, Moscow, 119991, Russian Federation

Доп.точки доступа:
Verpekin, V. V.; Ahremchik, I. S.; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Burmakina, G. V.; Kondrasenko, A. A.; Nedelina, T. S.; Kreindlin, A. Z.
}
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16.

    Polymer Films of Poly-3-hydroxybutyrate Synthesized byCupriavidus necatorfrom Different Carbon Sources / E. Shishatskaya, I. Nemtsev, A. Lukyanenko [et al.] // J. Polym. Environ. - 2021. - Vol. 29. - P. 837-850, DOI 10.1007/s10924-020-01924-3. - Cited References: 54. - The reported study was funded by RFBR and KKRF Grant No. 19-43-240012 "Biological and physical principles of production of new generation biomaterials". The work was carried out as part of the State Assignment of the Ministry of Education and Science of the Russian Federation No. FSRZ-2020-0006. The authors would like to express their special thanks to Krasnoyarsk Regional Center of Research Equipment of Federal Research Center "Krasnoyarsk Science Center SB RAS" for providing equipment to ensure the accomplishment of this project . - ISSN 1566-2543. - ISSN 1572-8919
   Перевод заглавия: Полимерные пленки Поли-3-гидроксибутирата, синтезированные некатором Cupriavidus из различных источников углерода

РУБ Engineering, Environmental + Polymer Science
Рубрики:
CHEMOMECHANICAL PROPERTIES
RALSTONIA-EUTROPHA
SURFACE-ROUGHNESS
Кл.слова (ненормированные):
Degradable P(3HB) -- Various carbon substrates -- Films -- Structure -- Properties -- NIH 3T3 fibroblasts
Аннотация: Films were prepared from 2% solutions of biodegradable poly-3-hydroxybutyrate [P(3HB)] and investigated. The polymer was synthesized by the Cupriavidus necator B-10646 bacterium cultivated using various carbon sources (glucose and glycerol of different degrees of purity, containing 0.3 to 17.93% impurities). Glycerol as the substrate influenced molecular-weight properties and crystallinity of the polymer without affecting its temperature characteristics. The P(3HB) specimens synthesized from glycerol had reduced Mw (300–400 kDa) and degree of crystallinity (50–55%) compared to the specimens synthesized from glucose (860 kDa and 76%, respectively). The low-crystallinity P(3HB) specimens, regardless of the degree of purity of glycerol, produced a beneficial effect on the properties of polymer films, which had a better developed folded surface and increased hydrophilicity. The values of the highest roughness (Ra) of the films synthesized from glycerol were 1.8 to 4.0 times lower and the water angles 1.4–1.6 times smaller compared to the films synthesized from glucose (71.75 nm and 87.4°, respectively). Those films performed better as cell scaffolds: the number of viable NIH fibroblasts was 1.7–1.9 times higher than on polystyrene (control) or films of P(3HB) synthesized from glucose.

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Держатели документа:
Siberian Fed Univ, 79 Svobodnyi Av, Krasnoyarsk 660041, Russia.
RAS, Krasnoyarsk Sci Ctr SB, Fed Res Ctr, Inst Biophys, Krasnoyarsk, Russia.
RAS, Krasnoyarsk Sci Ctr SB, Fed Res Ctr, LV Kirenskii Inst Phys, Krasnoyarsk, Russia.

Доп.точки доступа:
Shishatskaya, Ekaterina; Nemtsev, I. V.; Немцев, Иван Васильевич; Lukyanenko, A. V.; Лукьяненко, Анна Витальевна; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Kiselev, Evgeniy; Sukovatyi, Aleksey; Volova, Tatiana; RFBRRussian Foundation for Basic Research (RFBR); KKRF [19-43-240012]; Ministry of Education and Science of the Russian FederationMinistry of Education and Science, Russian Federation [FSRZ-2020-0006]
}
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17.

Эффект катионного замещения во фторкислородных молибдатах (NH)2-xAxMoO2F4 / Е. В. Богданов, А. Д. Васильев, И. Н. Флеров, Н. М. Лапташ // Физика твердого тела. - 2011. - Т. 53, № 2. - С. 284-288 . - ISSN 0367-3294
Аннотация: Выполнены теплофизические и структурные исследования твердых растворов оксифторидов (NH4)2-xAxMoO2F4 (A:Cs, Rb, K). Выяснен характер влияния катионных замещений на устойчивость исходной фазы (пр. гр. Cmcm) и механизм фазовых переходов. Работа выполнена при финансовой поддержке Российского фонда фундаментальных исследований (грант N 09-02-00062), гранта президента РФ для поддержки ведущих научных школ РФ (НШ-1011.2008.2).

РИНЦ
Держатели документа:
Институт инженерной физики и радиоэлектроники Сибирского федерального университета, Красноярск, Россия
Институт физики им. Л.В. Киренского СО РАН, Красноярск, Россия
Институт химии ДВО РАН, Владивосток, Россия

Доп.точки доступа:
Богданов, Евгений Витальевич; Bogdanov, E. V.; Васильев, Александр Дмитриевич; Vasiliev, A. D.; Флеров, Игорь Николаевич; Flerov, I. N.; Лапташ, Н. М.
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18.

Новые сведения о фазовом переходе в SrAlF5 / В. С. Бондарев, А. Д. Васильев, М. В. Горев [и др.] // Кристаллография. - 2011. - Т. 56, № 1. - С. 33-38 . - ISSN 0023-4761

ГРНТИ

31.15

Аннотация: Проведены исследования теплофизических характеристик кристалла SrAlF5 на образцах различного качества, а также анализ результатов по исследованию теплового расширения и двупреломления в процессах нагрева?охлаждения в интервале температур 100?800 К. Обнаружены аномалии теплоемкости, положение которых на шкале температур зависит от качества образцов и термической предыстории. Рентгеноструктурные исследования SrAlF5 показали отсутствие структурных фазовых переходов в исследованной области температур. Предполагается, что аномалии теплоемкости связаны с особенностью транспортных свойств данного кристалла.

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Держатели документа:
Институт геологии и минералогии СО РАН, Новосибирск
Институт физики СО РАН, Красноярск

Доп.точки доступа:
Бондарев, Виталий Сергеевич; Bondarev, V. S.; Васильев, Александр Дмитриевич; Vasiliev, A. D.; Горев, Михаил Васильевич; Gorev, M. V.; Мельникова, Светлана Владимировна; Mel'nikova, S. V.; Исаенко, Л. И.
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19.

Bacterial cellulose (BC) and BC composites: Production and properties / T. G. Volova, S. V. Prudnikova, E. G. Kiselev [et al.] // Nanomaterials. - 2022. - Vol. 12, Is. 2. - Ст. 192, DOI 10.3390/nano12020192. - Cited References: 113. - This research was financially supported by the State Assignment of the Ministry of Science and Higher Education of the Russian Federation No. FSRZ-2020-0006 . - ISSN 2079-4991

РУБ Chemistry, Multidisciplinary + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
SILVER NANOPARTICLES
GLUCONACETOBACTER-HANSENII
MICROBIAL CELLULOSE
Кл.слова (ненормированные):
bacterial cellulose -- composites -- production -- properties
Аннотация: The synthesis of bacterial cellulose (BC) by Komagataeibacter xylinus strain B-12068 was investigated on various C-substrates, under submerged conditions with stirring and in static surface cultures. We implemented the synthesis of BC on glycerol, glucose, beet molasses, sprat oil, and a mixture of glucose with sunflower oil. The most productive process was obtained during the production of inoculum in submerged culture and subsequent growth of large BC films (up to 0.2 m2 and more) in a static surface culture. The highest productivity of the BC synthesis process was obtained with the growth of bacteria on molasses and glycerol, 1.20 and 1.45 g/L per day, respectively. We obtained BC composites with silver nanoparticles (BC/AgNPs) and antibacterial drugs (chlorhexidine, baneocin, cefotaxime, and doripenem), and investigated the structure, physicochemical, and mechanical properties of composites. The disc-diffusion method showed pronounced antibacterial activity of BC composites against E. coli ATCC 25922 and S. aureus ATCC 25923.

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Держатели документа:
Siberian Fed Univ, Sch Fundamental Biol & Biotechnol, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.
RAS, Krasnoyarsk Sci Ctr SB, Fed Res Ctr, Inst Biophys SB, 50-50 Akademgorodok, Krasnoyarsk 660036, Russia.
RAS, Krasnoyarsk Sci Ctr SB, Fed Res Ctr, LV Kirensky Inst Phys SB, 50-38 Akademgorodok, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Siberian Branch, Krasnoyarsk Sci Ctr, Fed Res Ctr, 50 Akademgorodok, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Petr & Gas Engn, 79 Svobodny Pr, Krasnoyarsk 660041, Russia.

Доп.точки доступа:
Volova, Tatiana G.; Prudnikova, Svetlana V.; Kiselev, Evgeniy G.; Nemtsev, I. V.; Немцев, Иван Васильевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Kuzmin, Andrey P.; Shishatskaya, Ekaterina I.; Ministry of Science and Higher Education of the Russian Federation [FSRZ-2020-0006]
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20.

    The superexchange interactions in mixed Co-Fe ludwigite / N. V. Kazak [et al.] // J. Magn. Magn. Mater. - 2011. - Vol. 323, Is. 5. - P. 521-527, DOI 10.1016/j.jmmm.2010.09.057. - Cited Reference Count: 15. - Гранты: This study was supported by the Russian Foundation for Basic Research (Project no. 09-02-00171-a), the Federal Agency for Science and Innovation (Rosnauka) (Project no. MK-5632. 2010.2), Physical Division of the Russian Academy of Science, the program "Strongly Correlated Electrons", project 2.3.1.; The financial support of Spanish MINCYT, MAT08/1077 and Aragonese E-34 project are also acknowledged. - Финансирующая организация: Russian Foundation for Basic Research [09-02-00171-a]; Federal Agency for Science and Innovation (Rosnauka) [MK-5632. 2010.2]; Physical Division of the Russian Academy of Science; "Strongly Correlated Electrons" [2.3.1]; Spanish MINCYT [MAT08/1077]; Aragonese E-34 project . - MAR. - ISSN 0304-8853
Рубрики:
TRANSPORT-PROPERTIES
   SPECTRA
Кл.слова (ненормированные):
ludwigite structure -- magnetic susceptibility -- magnetic frustration -- mott conductivity -- ludwigite structure -- magnetic frustration -- magnetic susceptibility -- mott conductivity -- ac susceptibility -- cation distributions -- crystal data -- crystallographic sites -- electrical resistivity -- iron atoms -- low temperatures -- ludwigite structure -- magnetic behavior -- magnetic frustrations -- magnetic system -- magnetic transitions -- mossbauer -- mossbauer effects -- mott conductivity -- mott hopping -- superexchange energy -- superexchange interaction -- temperature regions -- trivalent iron -- variable range -- cobalt -- electric conductivity -- magnetic susceptibility -- magnetism -- mossbauer spectroscopy -- x ray diffraction -- crystal structure
Аннотация: The crystal structure, cation distribution and exchange interactions in the Co2.25Fe0.75O2BO3 ludwigite have been explored through X-ray diffraction, electrical resistivity, ac-susceptibility and Mossbauer effect measurements. The crystal data have shown that iron atoms occupy the most symmetric crystallographic sites Fe4 and Fe2. The complex magnetic behavior with two magnetic transitions near 70 and 115 K at low temperatures was found. The Mossbauer data have displayed the trivalent iron states only. The values of superexchange energies have been estimated for Co3O2BO3 and Co2.25Fe0.75O2BO3 yielding a significant role of frustrations in the ludwigite magnetic system. Variable range Mott hopping conductivity law was proved to be valid in the wide temperature region, pointing out a localized character of charge carriers rather than collective. (C) 2010 Elsevier B.V. All rights reserved.

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Держатели документа:
RAS, LV Kirensky Phys Inst, SB, Krasnoyarsk 660036, Russia
Siberian Fed Univ, Krasnoyarsk 660074, Russia
Krasnoyarsk State Agr Univ, Krasnoyarsk 660049, Russia
Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, Abd Dept Fis Mat Condensada, E-50009 Zaragoza, Spain
Univ Zaragoza, Area Medidas Fis, Serv Instrumentac Cient, E-50009 Zaragoza, Spain

Доп.точки доступа:
Kazak, N. V.; Казак, Наталья Валерьевна; Bayukov, O. A.; Баюков, Олег Артемьевич; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Vasiliev, A. D.; Васильев, Александр Дмитриевич; Rudenko, V. V.; Руденко, Валерий Васильевич; Ivanova, N. B.; Иванова, Наталья Борисовна; Knyazev, Yu. V.; Князев, Юрий Владимирович; Bartolom, J.; Arauzo, A.
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