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1.


   
    Synthesis and characterization of core-shell magnetic nanoparticles NiFe2O4@Au / D. Saykova, S. Saikova, Y. Mikhlin [et al.] // Metals. - 2020. - Vol. 10, Is. 8. - Ст. 1075, DOI 10.3390/met10081075. - Cited References: 45 . - ISSN 2075-4701
   Перевод заглавия: Синтез и характеристика магнитных наночастиц ядро-оболочка NiFe2O4@Au
РУБ Materials Science, Multidisciplinary + Metallurgy & Metallurgical
Рубрики:
NICKEL FERRITE NANOPARTICLES
   GOLD NANOPARTICLES

   OXIDATION

   REDUCTION

Кл.слова (ненормированные):
nickel ferrite nanoparticles -- NiFe2O4@Au core-shell nanoparticles -- synthesis -- X-ray photoelectron spectroscopy -- magnetic circular dichroism
Аннотация: In this study, NiFe2O4@Au core–shell nanoparticles were prepared by the direct reduction of gold on the magnetic surface using amino acid methionine as a reducer and a stabilizing agent simultaneously. The obtained nanoparticles after three steps of gold deposition had an average size of about 120 nm. The analysis of particles was performed by X-ray diffraction, transmission electron microscopy, X-ray photoelectron spectroscopy, and UV-Vis spectroscopy techniques. The results indicate successful synthesis of core–shell particles with the magnetic core, which consists of a few agglomerated nickel ferrite crystals with an average size 25.2 ± 2.0 nm, and the thick gold shell consists of fused Au0 nanoparticles (NPs). Magnetic properties of the obtained nanoparticles were examined with magnetic circular dichroism. It was shown that the magnetic behavior of NiFe2O4@Au NPs is typical for superparamagnetic NPs and corresponds to that for NiFe2O4 NPs without a gold shell. The results indicate the successful synthesis of core–shell particles with the magnetic nickel ferrite core and thick gold shell, and open the potential for the application of the investigated hybrid nanoparticles in hyperthermia, targeted drug delivery, magnetic resonance imaging, or cell separation. The developed synthesis strategy can be extended to other metal ferrites and iron oxides.

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Держатели документа:
Siberian Fed Univ, Sch Nonferrous Met & Mat Sci, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Siberian Branch, Inst Chem & Chem Technol, Fed Res Ctr,Krasnoyarsk Sci Ctr, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Kirensky Inst Phys, Fed Res Ctr, Krasnoyarsk Sci Ctr,Siberian Branch, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Saykova, Diana; Saikova, Svetlana; Mikhlin, Yuri; Panteleeva, Marina; Ivantsov, R. D.; Иванцов, Руслан Дмитриевич; Belova, E.
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2.


   
    High-temperature evolution of the magnetization of aluminum reduction cell steel / D. A. Balaev, S. V. Semenov, S. N. Varnakov [et al.] // J. Sib. Fed. Univ. Math. Phys. - 2021. - Vol. 14, Is. 1. - P. 5-11 ; Журн. СФУ. Матем. и физика, DOI 10.17516/1997-1397-2021-14-1-5-11. - Cited References: 17. - We are grateful to A. D. Balaev and S. V.Komogortsev for fruitful discussions. The magnetic measurements were performed on the facility at the Krasnoyarsk Territorial Center for Collective Use, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences. This study was supported by the Russian Foundation for Basic Research, the Government of the Krasnoyarsk Territory, the Krasnoyarsk Territorial Foundation for Support of Scientific and R&D Activities, and the United Company RUSAL, project no. 20-48-242905 "Determining the Effect of Magnetization of Ferromagnets on the MHD Parameters of the Reduction Cell" . - ISSN 1997-1397
   Перевод заглавия: Высокотемпературная эволюция намагниченности стали алюминиевого электролизера
Кл.слова (ненормированные):
steel -- aluminum reduction cells -- saturation magnetization -- Bloch’s constant -- сталь -- алюминиевые ячейки восстановления -- намагниченность насыщения -- постоянная Блоха
Аннотация: The magnetic properties of steel of a structural element of an aluminum reduction cell have been investigated in the temperature range of 300–900 K. The analysis of the temperature dependence of the saturation magnetization Ms(T) showed (i) the applicability of the Bloch’s 3/2 law and a reason- able value of the Bloch’s constant for steel and (ii) the quadratic dependence Ms(T)~(1 - T2) in the temperature range of 380–700 K.
В работе исследованы магнитные свойства стали конструктивного элемента алюминиевого электролизера в области температур 300–900 K. Проведенный анализ температурной зависимости намагниченности насыщения MS(T) показал: (i) применимость "закона 3/2" Блоха, а также разумное значение константы Блоха и константы обменного взаимодействия для стали; (ii) квадратичную зависимость MS(T)∼(1 - T2) в температурном диапазоне 380–700 K.

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

Доп.точки доступа:
Balaev, D. A.; Балаев, Дмитрий Александрович; Semenov, S. V.; Семёнов, Сергей Васильевич; Varnakov, S. N.; Варнаков, Сергей Николаевич; Radionov, E. Y.; Tretyakov, Al. Y.

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3.


   
    Structural changes of Co caused a change of the solution pH during chemical deposition / S. A. Podorozhnyak, A. V. Chzhant, V. K. Maltsevt [et al.] // J. Sib. Fed. Univ. Math. Phys. - 2020. - Vol. 13, Is. 4. - P. 451-458 ; Журн. СФУ. Матем. и физика, DOI 10.17516/1997-1397-2020-13-4-451-458. - Cited References: 10 . - ISSN 1997-1397. - ISSN 2313-6022
   Перевод заглавия: Структурные изменения кобальта, вызванные изменением pH при химическом осаждении
РУБ Mathematics
Рубрики:
COBALT
   MICROSTRUCTURE

Кл.слова (ненормированные):
Co-P films -- chemical reduction of metals -- induced magnetic anisotropy -- nanocrystalline material -- пленки Co-P -- химическое восстановление металлов -- наведенная магнитная анизотропия -- нанокристаллический материал
Аннотация: The phase transformations of the Co lattice are discussed, which determine the anomalous changes in the magnetic properties of chemically deposited Co-P films obtained at various pH values. The coercivity of the H-c films obtained at low pH values exceeds 1 kOe and decreases to several units Oe in the films obtained at high pH values. It is shown that the observed changes in the magnetic properties of Co-P films are caused by the transition of the cobalt crystal lattice to the nanocrystalline state.
Обсуждаются фазовые превращения решетки Co, которые определяют аномальные изменения магнитных свойств химически осажденных пленок Co-P, полученных при различных значениях pH. Коэрцитивная сила пленок, полученных при низких значениях pH, превышает 1 кЭ и снижается до нескольких единиц Э в пленках, полученных при высоких значениях pH. Показано, что наблюдаемые изменения магнитных свойств пленок Co-P вызваны переходом кристаллической решетки кобальта в нанокристаллическое состояние.

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Держатели документа:
Siberian Fed Univ, Krasnoyarsk, Russia.
Krasnoyarsk State Agr Univ, Krasnoyarsk, Russia.
RAS, Kirensky Inst Phys FIC KNC SB, Krasnoyarsk, Russia.

Доп.точки доступа:
Podorozhnyak, Sergey A.; Chzhant, Anatoly, V; Maltsevt, Vadim K.; Krayuhin, Ivan N.; Patrin, G. S.; Патрин, Геннадий Семёнович; Sakash, Irina Yu

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4.


   
    Novel Derivatives of Adamantyl-substituted Quinolin-6-amines and Synthesis of Imidazo[4,5-f]quinolines Therefrom / A. A. Abramov [et al.] // Russ. J. Organ. Chem. - 2019. - Vol. 55, Is. 8. - P. 1234-1237, DOI 10.1134/S1070428019080256. - Cited References: 7 . - ISSN 1070-4280. - ISSN 1608-3393
РУБ Chemistry, Organic

Кл.слова (ненормированные):
amination -- adamantanylalkylamines -- reduction -- cyclization -- 5-nitroso-6-quinolinamines -- quinoline-5,6-diamines -- 3H-imidazo[4,5-f]quinolines
Аннотация: N-(Adamantan-1-yl)alkyl-substituted 5-nitrosoquinolin-6-amines were synthesized for the first time by the amination of 5-nitrosoquinolin-6-ol with primary N-[(adamantan-1-yl)alkyl]amines. The resulting nitrosoquinolinamines were reduced with hydrazine hydrate over Pd/C to N6-[(adamantan-1-yl)alkyl]quinoline-5,6-diamines. The latter were heated in formic acid to obtain previously unknown 3-[(adamantan-1-yl)alkyl]-3H-imidazo[4,5-f]quinolines.

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Держатели документа:
Reshetnev Siberian State Univ Sci & Technol, Pr Im Gazety Krasnoyarskii Rabochii 31, Krasnoyarsk 660037, Russia.
Russian Acad Sci, Inst Chem & Chem Technol, Siberian Branch, Krasnoyarsk Res Ctr, Akad Gorodok 50,Stroenie 24, Krasnoyarsk 660036, Russia.
Russian Acad Sci, Krasnoyarsk Res Ctr, Siberian Branch, Kirenskii Inst Phys, Akad Gorodok 50,Stroenie 38, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Abramov, A. A.; Kulagina, M. V.; Gavrilova, N. A.; Semichenko, E. S.; Kondrasenko, A. A.; Suboch, G. A.
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5.


   
    Ion reduction in iron oxide and oxyhydroxide nanoparticles during ultrasonic treatment / S. V. Stolyar [et al.] // Euro-asian symposium "Trends in magnetism" (EASTMAG-2019) : Book of abstracts / чл. конс. ком.: S. G. Ovchinnikov, N. V. Volkov [et al.] ; чл. прогр. ком. D. M. Dzebisashvili [et al.]. - 2019. - Vol. 1. - Ст. C.P12. - P. 291. - Cited References: 6. - The reported study was carried out with the financial support of the Russian Foundation for Fundamental Research, the Government of the Krasnoyarsk Territory, the Krasnoyarsk Territory Fund for Support of Scientific and Technical Activity in the framework of scientific Projects No. 18-43-243003 and No. 18-42-243011. The work is supported by the Special Program of the Ministry of Education and Science of the Russian Federation for the Siberian Federal University . - ISBN 978-5-9500855-7-4

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

Доп.точки доступа:
Ovchinnikov, S. G. \чл. конс. ком.\; Овчинников, Сергей Геннадьевич; Volkov, N. V. \чл. конс. ком.\; Волков, Никита Валентинович; Dzebisashvili, D. M. \чл. прогр. ком.\; Дзебисашвили, Дмитрий Михайлович; Stolyar, S. V.; Столяр, Сергей Викторович; Bayukov, O. A.; Баюков, Олег Артемьевич; Yaroslavtsev, R. N.; Ярославцев, Роман Николаевич; Knyazev, Yu. V.; Князев, Юрий Владимирович; Ladygina, V. P.; Gerasimova, Y. V.; Герасимова, Юлия Валентиновна; Iskhakov, R. S.; Исхаков, Рауф Садыкович; Российская академия наук; Уральское отделение РАН; Институт физики металлов им. М. Н. Михеева Уральского отделения РАН; Уральский федеральный университет им. первого Президента России Б.Н. Ельцина; Российский фонд фундаментальных исследований; Euro-Asian Symposium "Trends in MAGnetism"(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg); "Trends in MAGnetism", Euro-Asian Symposium(7 ; 2019 ; Sept. ; 8-13 ; Ekaterinburg)
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6.


   
    Hydrogenation of levulinic acid to gamma-valerolactone in the presence of Ru-containing catalysts based on carbon material "Sibunit" / V. V. Sychev, S. V. Baryshnikov, I. P. Ivanov [et al.] // J. Sib. Fed. Univ. Chem. - 2021. - Vol. 14, Is. 1. - P. 5-20 ; Журн. СФУ. Химия, DOI 10.17516/1998-2836-0211. - Cited References: 28. - This work was financially supported by the Russian Foundation for Basic Research (RFBR) (project No. 20-03-00636) . - ISSN 1998-2836. - ISSN 2313-6049
   Перевод заглавия: Гидрирование левулиновой кислоты до γ-валеролактона в присутствии Ru-содержащих катализаторов на основе углеродного материала Сибунит
РУБ Chemistry, Multidisciplinary
Рубрики:
BIOMASS
   RUTHENIUM

   DEHYDRATION

   SELECTIVITY

   CONVERSION

   CELLULOSE

Кл.слова (ненормированные):
heterogeneous catalysis -- gamma-valerolactone -- levulinic acid -- alkyl levulinates -- hydrogenation -- reduction -- ruthenium -- Ru/C -- гетерогенный катализ -- гамма-валеролактон -- левулиновая кислота -- алкиллевулинаты -- гидрирование -- восстановление -- рутений -- Ru/C
Аннотация: Nanostructured 1 and 3% catalysts containing ruthenium nanoparticles supported on the initial and oxidized at different temperatures graphite-like carbon material Sibunit-4 prepared. A features of this support are mesoporous texture, hydrothermal stability and the presence of surface oxygen-containing functional groups responsible for the distribution of Ru nanoparticles and the catalyst acidic properties. The catalysts characterized using methods TEM, XPS, N2 adsorption, pHpzc and tested in the hydrogenation of levulinic acid to γ-valerolactone. It was found that the reaction rate and GVL selectivity are influenced by solvent choice, fractional composition, and acidic properties of the support. The obtained catalysts provide high activity in the reaction of direct hydrogenation of levulinic acid to γ-valerolactone (GVL yield 98 mol.%, At 160°С, 1.2 MPa H2) and high productivity (15.9 gGVL/gCat.). Obtained catalyst can be reused several times without noticeable loss of activity.
Синтезированы наноструктурированные 1 и 3 % катализаторы, содержащие наночастицы рутения, закрепленные на исходном и окисленном при разных температурах графитоподобном углеродном материале Cибунит‑4. Особенность данного носителя состоит в его мезопористой текстуре, гидротермальной устойчивости и наличии на поверхности кислородсодержащих функциональных групп, ответственных за распределение наночастиц Ru и кислотные свойства катализатора. Катализаторы исследованы физико-химическими методами (ПЭМ, РФЭС, адсорбция N2, pHтнз) и испытаны в реакции гидрирования левулиновой кислоты до γ-валеролактона. Установлено, что на скорость реакции и селективность процесса по отношению к ГВЛ оказывают влияние такие факторы, как выбранный растворитель, фракционный состав и кислотные свойства носителя. Полученные катализаторы показали высокую активность в реакции прямого гидрирования левулиновой кислоты до γ-валеролактона (выход ГВЛ 98 мол.% при 160 ºС, 1.2 МПа H2) и высокую производительность (15.9 г ГВЛ/г кат.). Данный катализатор может быть использован многократно без заметной потери активности.

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Держатели документа:
FRC Krasnoyarsk Sci Ctr SB RAS, Inst Chem & Chem Technol SB RAS, Krasnoyarsk, Russia.
Kirensky Inst Phys SB RAS, Krasnoyarsk, Russia.
Siberian Fed Univ, Krasnoyarsk, Russia.

Доп.точки доступа:
Sychev, Valentin V.; Baryshnikov, S. V.; Ivanov, Ivan P.; Volochaev, M. N.; Волочаев, Михаил Николаевич; Taran, Oxana P.; Russian Foundation for Basic Research (RFBR)Russian Foundation for Basic Research (RFBR) [20-03-00636]

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7.


   
    The relationship between the structural characteristics of α-Fe2O3 catalysts and their lattice oxygen reactivity regarding hydrogen / N. Kirik, A. Krylov, A. Boronin [et al.] // Materials. - 2023. - Vol. 16, Is. 12 : The 15th Anniversary of Materials — Recent Advances in Catalytic Materials. - Ст. 4466, DOI 10.3390/ma16124466. - Cited References: 63. - This work was conducted within the framework of the budget project for the Institute of Chemistry and Chemical Technology of the Siberian Branch of the Russian Academy of Sciences, Federal Research Center KSC SB RAS, No. FWES–2021–0013 . - ISSN 1996-1944
Кл.слова (ненормированные):
α-Fe2O3 -- catalysts -- calcinations -- XRD -- XPS -- Raman spectroscopy characterization -- temperature-programmed reduction
Аннотация: In this paper, the relationship between the structural features of hematite samples calcined in the interval of 800–1100 °C and their reactivity regarding hydrogen studied in the temperature-programmed reaction (TPR-H2) was studied. The oxygen reactivity of the samples decreases with the increasing calcination temperature. The study of calcined hematite samples used X-ray Diffraction (XRD), Scanning Electron Microscopy (SEM), X-ray Photoelectron Spectroscopy (XPS), and Raman spectroscopy, and their textural characteristics were studied also. According to XRD results, hematite samples calcined in the temperature range under study are monophase, represented by the α-Fe2O3 phase, in which crystal density increases with increasing calcination temperature. The Raman spectroscopy results also register only the α-Fe2O3 phase; the samples consist of large, well-crystallized particles with smaller particles on their surface, having a significantly lower degree of crystallinity, and their proportion decreases with increasing calcination temperature. XPS results show the α-Fe2O3 surface enriched with Fe2+ ions, whose proportion increases with increasing calcination temperature, which leads to an increase in the lattice oxygen binding energy and a decrease in the α-Fe2O3 reactivity regarding hydrogen.

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Держатели документа:
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Institute of Chemistry and Chemical Technology, 50/24, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center “Krasnoyarsk Science Center of Siberian Branch of the Russian Academy of Sciences”, Kirensky Institute of Physics, 50/38, Akademgorodok, 660036 Krasnoyarsk, Russia
Federal Research Center Boreskov Institute of Catalysis, 5, Ac. Lavrentieva Ave., 630090 Novosibirsk, Russia
Department of Chemistry, 79, Svobodny Ave., Siberian Federal University, 660041 Krasnoyarsk, Russia

Доп.точки доступа:
Kirik, N.; Krylov, A. S.; Крылов, Александр Сергеевич; Boronin, A.; Koshcheev, S.; Solovyov, L.; Rabchevskii, E.; Shishkina, N.; Anshits, A.
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8.


   
    The low-temperature germinating spores of the thermophilic Desulfofundulus contribute to an extremely high sulfate reduction in burning coal seams / O. V. Karnachuk, I. I. Rusanov, I. A. Panova [et al.] // Front. Microbiol. - 2023. - Vol. 14. - Ст. 1204102, DOI 10.3389/fmicb.2023.1204102. - Cited References: 80. - This study was supported by the Russian Science Foundation Projects 21-14-00114 (to OK, sampling, sulfate reduction rate measurements, pure culture isolation and physiological experiments with pure culture and spores) and 22-14-00178 (to NR, metagenome and genome sequencing and analysis) and the Ministry of Science and Higher Education of the Russian Federation . - ISSN 1664-302X
Кл.слова (ненормированные):
sulfate reduction -- thermophiles -- burning coal seams -- Desulfofundulus -- spores
Аннотация: Burning coal seams, characterized by massive carbon monoxide (CO) emissions, the presence of secondary sulfates, and high temperatures, represent suitable environments for thermophilic sulfate reduction. The diversity and activity of dissimilatory sulfate reducers in these environments remain unexplored. In this study, using metagenomic approaches, in situ activity measurements with a radioactive tracer, and cultivation we have shown that members of the genus Desulfofundulus are responsible for the extremely high sulfate reduction rate (SRR) in burning lignite seams in the Altai Mountains. The maximum SRR reached 564 ± 21.9 nmol S cm−3 day−1 at 60°C and was of the same order of magnitude for both thermophilic (60°C) and mesophilic (23°C) incubations. The 16S rRNA profiles and the search for dsr gene sequences in the metagenome revealed members of the genus Desulfofundulus as the main sulfate reducers. The thermophilic Desulfofundulus sp. strain Al36 isolated in pure culture, did not grow at temperatures below 50°C, but produced spores that germinated into metabolically active cells at 20 and 15°C. Vegetative cells germinating from spores produced up to 0.738 ± 0.026 mM H2S at 20°C and up to 0.629 ± 0.007 mM H2S at 15°C when CO was used as the sole electron donor. The Al36 strain maintains significant production of H2S from sulfate over a wide temperature range from 15°C to 65°C, which is important in variable temperature biotopes such as lignite burning seams. Burning coal seams producing CO are ubiquitous throughout the world, and biogenic H2S may represent an overlooked significant flux to the atmosphere. The thermophilic spore outgrowth and their metabolic activity at temperatures below the growth minimum may be important for other spore-forming bacteria of environmental, industrial and clinical importance.

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Держатели документа:
Laboratory of Biochemistry and Molecular Biology, Tomsk State University, Tomsk, Russia
Institute of Microbiology, Research Centre of Biotechnology of the Russian Academy of Sciences, Moscow, Russia
Institute of Bioengineering, Research Centre of Biotechnology of the Russian Academy of Sciences, Moscow, Russia
Kirensky Institute of Physics, Krasnoyarsk, Russia

Доп.точки доступа:
Karnachuk, O. V.; Rusanov, I. I.; Panova, I. A.; Kadnikov, V. V.; Avakyan, M. R.; Ikkert, O. P.; Lukina, A. P.; Beletsky, A. V.; Mardanov, A. V.; Knyazev, Yu. V.; Князев, Юрий Владимирович; Volochaev, M. N.; Волочаев, Михаил Николаевич; Pimenov, N. V.; Ravin, N. V.
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9.


   
    Chemistry of vinylidene complexes. 6. Electrochemical reduction and UV spectra of vinylidene derivatives of cymantrene and complexes with an Mn-Pt bond [Text] / A. A. Ioganson [et al.] // Bulletin of the Academy of Sciences of the USSR. Division of Chemical Sciences. - 1987. - Т. 36, № 1. - P46-50, DOI 10.1007/BF00953843 . - ISSN 1066-5285. - ISSN 1573-9171
ГРНТИ


РИНЦ
Держатели документа:
Institute of Chemistry and Chemical Engineering,Academy of Sciences of the USSR, Siberian Branch
Доп.точки доступа:
Ioganson, A.A.; Antonova, A.B.; Trukhacheva, V.A.; Brumakina, G.V.; Rubailo, A.I.; Maksimov, N.G.; Kovalenko, S.V.; Deikhina, N.A.
}
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    Biogenic ferrihydrite nanoparticles produced by Klebsiella oxytoca: Characterization, physicochemical properties and bovine serum albumin interactions / N. Cazacu, C. G. Chilom, S. Iftimie [et al.] // Nanomaterials. - 2022. - Vol. 12, Is. 2. - Ст. 249, DOI 10.3390/nano12020249. - Cited References: 59. - This research was funded by JINR Themes 02-1-1107-2011/2021, 04-5-1131-2017/2021 and 04-4-1133-2018/2023 and with the financial support of the RO-JINR Projects Nos. 366/11.05.2021 (items 7, 86, 97) and 365/11.05.2021 (items 8, 87 and 98). This work also benefited from the use of the SasView application, originally developed under NSF Award DMR-0520547. SasView also contains the code developed with funding from the EU Horizon 2020 program under the SINE2020 project Grant No 654000. The APC was funded by JINR Theme 02-1-1107-2011/2021, Project No. 366/11.05.2021, item 7. This study used the infrastructure of the Applied Genetics Resource Facility of MIPT (Suport Grant 075-15-2021-684) . - ISSN 2079-4991
РУБ Chemistry, Multidisciplinary + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
MAGNETIC-PROPERTIES
   REDUCTION

   MOSSBAUER

   FERRITIN

   DOCKING

   BINDING

Кл.слова (ненормированные):
biogenic ferrihydrite nanoparticles -- the binding mechanism -- energy transfer -- protein stability -- molecular docking
Аннотация: The synthesis of nanoparticles inside microorganisms is an economical alternative to chemical and physical methods of nanoparticle synthesis. In this study, ferrihydrite nanoparticles synthesized by Klebsiella oxytoca bacterium in special conditions were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray analysis (EDS), small-angle X-ray (SAXS), UV-Vis spectroscopy, fluorescence, fluorescence resonance energy transfer (FRET), and molecular docking. The morphology and the structure of the particles were characterized by means of SEM and SAXS. The elemental content was determined by means of the EDS method. The absorption properties of the ferrihydrite nanoparticles were investigated by UV-Vis spectroscopy. The binding mechanism of the biogenic ferrihydrite nanoparticles to Bovine Serum Albumin (BSA) protein, studied by fluorescence, showed a static and weak process, combined with FRET. Protein denaturation by temperature and urea in the presence of the ferrihydrite nanoparticles demonstrated their influence on the unfolding process. The AutoDock Vina and UCSF Chimera programs were used to predict the optimal binding site of the ferrihydrite to BSA and to find the location of the hydrophobic cavities in the sub-domain IIA of the BSA structure.

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Держатели документа:
Univ Bucharest, Fac Phys, Dept Elect Solid State & Biophys, RO-077125 Magurele, Romania.
Horia Hulubei Natl Inst Phys & Nucl Engn, Dept Nucl Phys, RO-077125 Magurele, Romania.
Joint Inst Nucl Res, Dubna 141980, Russia.
Moscow Inst Phys & Technol, Dolgoprudnyi 141701, Russia.
Russian Acad Sci, Siberian Branch, Fed Res Ctr KSC, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Sch Engn Phys & Radio Elect, Phys Dept, Krasnoyarsk 660041, Russia.
Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Cazacu, Nicoleta; Chilom, Claudia G.; Iftimie, Sorina; Balasoiu, Maria; Ladygina, Valentina P.; Stolyar, S. V.; Столяр, Сергей Викторович; Orelovich, Oleg L.; Kovalev, Yuriy S.; Rogachev, Andrey V.
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