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    Raman study of structural transformations in self-assembled diphenylalanine nanotubes at elevated temperatures / P. S. Zelenovskiy [et al.] // J. Raman Spectrosc. - 2017. - Vol. 48, Is. 11. - P. 1401-1405, DOI 10.1002/jrs.5084. - Cited References:50. - The equipment of the Ural Center for Shared Use 'Modern nanotechnology' UrFU was used. The research was supported by the President of Russian Federation grant for young scientists (Contract 14.Y30.15.6554-MK) and by the Government of the Russian Federation (Act 211, Agreement 02.A03.21.0006). A.K. acknowledges the Turkish-Portuguese project TUBITAK/0006/2014 and CICECO-Aveiro Institute of Materials (Ref. FCT UID/CTM/50011/2013) financed by national funds through the FCT/MEC and, when applicable, co-financed by FEDER under the PT2020 Partnership Agreement. . - ISSN 0377-0486. - ISSN 1097-4555
   Перевод заглавия: Исследование структурных превращений в самоорганизованных дифенилаланиновых нанотрубках при повышенных температурах методом комбинационного рассеяния света

РУБ Spectroscopy
Рубрики:
PEPTIDE NANOTUBES
   PIEZOELECTRIC PROPERTIES
   WATER
   MICROTUBES
Кл.слова (ненормированные):
peptide nanotubes -- diphenylalanine -- phase transition -- cyclization -- water
Аннотация: Self-assembled peptide diphenylalanine (NH2-Phe-Phe-COOH, FF) is one of the most important emergent functional materials, demonstrating wide range of fascinating physical and chemical properties including biocompatibility, chemical variability, exceptional rigidity, outstanding piezoelectric, pyroelectric and ferroelectric responses. Up to now, the phase transitions in FF nanotubes were investigated by scanning and transmission electron microscopy, atomic force microscopy, differential scanning calorimetry, thermogravimetry and mass spectroscopy. The Raman spectroscopy was implemented at room temperature only, and the microscopic details of these transitions remained unknown. In this work, the structural transformations in FF nanotubes at elevated temperatures (up to tubes destruction at 160 °C) were studied by Raman spectroscopy. Two structural transformations were observed in this region: hexagonal to orthorhombic transition at about 100 °C and the cyclization of FF molecules at about 150 °C. For the first time, these transformations were considered in the context of reconstruction of the water subsystem in the nanotubes, thus demonstrating the strong relation between the peptide tube and the state of the water inside. Using an effective frequency of nanotubes' lattice vibrations, we found that many effects observed earlier by other methods are induced by the variation of the water subsystem. The analysis of certain lines in the middle part of the Raman spectrum allowed us to describe the microscopic details of FF molecule cyclization. These results improve the understanding of the role of water in the origin of outstanding properties of FF nanotubes and thus promote developing new functional devices on their basis.

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Доп.точки доступа:
Zelenovskiy, P. S.; Davydov, A. O.; Krylov, A. S.; Крылов, Александр Сергеевич; Kholkin, A. L.; International GeoRAMAN Conference(12th ; June 9-15, 2016 ; Novosibirsk, Russia)
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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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Публикация на русском языке

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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