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

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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Elesina V. I., Churilov G. N., Vnukova N. G., Dudnik A. I., Osipova I. V.
Заглавие : Filtration process combined with mechanical action, as a method for efficient extraction of endohedral metallofullerenes from carbon soot
Место публикации : Fuller. Nanotub. Carbon Nanostruct. - 2019. - Vol. 27, Is. 10. - P.803-807. - ISSN 1536383X (ISSN), DOI 10.1080/1536383X.2019.1648439
Примечания : Cited References: 22
Аннотация: The paper presents results of fullerenes and endohedral metallofullerenes extracts studies, isolated from the graphite rods carbon soot spray, and containing Y2O3 in a high frequency arc discharge. Two ways of extraction were applied and compared–(1) the classic method of Soxhlet extraction, and (2) the one developed by our team–extraction based on mechanical action combined with filtration. To implement the method, we used a laboratory version of installation, embodying technical solutions for rapid extraction. Chromatographic and mass spectrometry studies of fullerene extracts obtained by these methods revealed that by combining mechanical action with simultaneous filtration, we can significantly intensify and reduce the process of extracting fullerenes and endohedral metallofullerenes compared to the Soxhlet extraction method. This is especially evident in the release of endohedral metallofullerenes. Our method allows to reduce the release time of fullerenes from 10 g of carbon soot on laboratory installation up to 15 minutes, against the Soxhlet extraction method taking 18 hours. Whilst, the total number of fullerenes extracted by both methods almost coincides (the extraction method using mechanical action allowed us to extract 0.2-0.4 wt. % more), the composition of the isolated fullerene mixtures is different. The relative content of higher fullerenes and endohedral metallofullerenes exceeds when the mechanical action-based extraction method applied. © 2019, © 2019 Taylor & Francis Group, LLC.
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Вид документа : Статья из сборника (выпуск продолж. издания)
Шифр издания :
Автор(ы) : Tomilin F. N., Rogova A. V., Kaufman E. V., Drevolsky A. S., Gerasimova M. A., Slyusareva E. A.
Заглавие : Solvent effect in the theoretical absorption and emission spectra of fluorescein dyes
Коллективы : International Conference on Pulsed Lasers and Laser Applications
Место публикации : International Conference on Pulsed Lasers and Laser Applications (14 ; 2019 ; 15-20 Sept. ; Tomsk). Proceedings of SPIE - The International Society for Optical Engineering. - 2019. - Vol. 11322: XIV International Conference on Pulsed Lasers and Laser Applications, AMPL 2019 (15-20 September 2019) Conference code: 156656. - Ст.113220O. - , DOI 10.1117/12.2548739
Примечания : Cited References: 13. - This work was supported by the Russian Foundation for Basic Research, project 19-02-00450
Аннотация: Fluorescein and its halogenated derivatives representing a family of homologous dyes with the gradual substitution of halogen atoms for hydrogen ones are widely used in biomedicine as fluorescent probes. This stimulates the intense experimental and theoretical studies of their fluorescent properties in aqueous solutions. However, the theoretical calculations are complicated by the necessity of taking into account the effect of a solvent (water) in the explicit form and the need for effective basic sets. This is especially important for the dyes that contain heavy atoms. In this study, the quantum-chemical investigations of the dianionic form of fluorescein and its Br- and I-substituted derivatives (eosin Y and erythrosin B) have been carried out using the time-dependent density functional theory (B3LYP functional) implemented in the GAMESS software suite. The effect of a solvent has been considered in the framework of the modified Thomas polarizable continuum model. The calculations have been made for vertical (absorption and emission) excitations in the adiabatic approximation and at the nonequilibrium solvation. The results obtained for the nonequilibrium solvation are in excellent agreement with the experimental data for fluorescein and its halogenated derivatives.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xiao, Hui, Dang, Peipei, Yun, Xiaohan, Li, Guogang, Wei, Yi, Wei, Yi, Xiao, Xiao, Zhao, Yajie, Molokeev M. S., Cheng, Ziyong, Lin, Jun
Заглавие : Solvatochromic photoluminescent effects in all-inorganic manganese(II)-based perovskites by highly selective solvent-induced crystal-to-crystal phase transformations
Место публикации : Angew. Chem. - 2021. - Vol. 133, Is. 7. - P.3743-3751. - ISSN 1521-3757 (eISSN), DOI 10.1002/ange.202012383
Примечания : Cited References: 73. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018)
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Xiao, Hui, Dang, Peipei, Yun, Xiaohan, Li, Guogang, Wei, Y.i., Xiao, Xiao, Zhao, Yajie, Molokeev M. S., Cheng, Ziyong, Lin, Jun
Заглавие : Solvatochromic Photoluminescent Effects in All-Inorganic Manganese(II)-Based Perovskites by Highly Selective Solvent-Induced Crystal-to-Crystal Phase Transformations
Место публикации : Angew. Chem. Int. Edit. - 2021. - Vol. 60, Is. 7. - P.3699-3707. - ISSN 1433-7851, DOI 10.1002/anie.202012383. - ISSN 1521-3773(eISSN)
Примечания : Cited References: 85. - This work was supported by National Natural Science Foundation of China (NSFC 51932009, 51772288, 52072349, 51672259) and the Joint Fund Project to Promote Science and Technology Cooperation Across the Taiwan Straits (U2005212), the Science and Technology Cooperation Fund between Chinese and Australian Governments (2017YFE0132300), CAS-Croucher Funding Scheme for Joint Laboratories (CAS18204), Chinese Academy of Sciences (YZDY-SSWJSC018)
Предметные рубрики: LEAD-FREE
HALIDE PEROVSKITE
NANOCRYSTALS
MN2+
LUMINESCENCE
Аннотация: The development of lead‐free perovskite photoelectric materials has been an extensive focus in the recent years. Herein, a novel one‐dimensional (1D) lead‐free CsMnCl3(H2O)2 single crystal is reported with solvatochromic photoluminescence properties. Interestingly, after contact with N,N‐dimethylacetamide (DMAC) or N,N‐dimethylformamide (DMF), the crystal structure can transform from 1D CsMnCl3(H2O)2 to 0D Cs3MnCl5 and finally transform into 0D Cs2MnCl4(H2O)2. The solvent‐induced crystal‐to‐crystal phase transformations are accompanied by loss and regaining of water of crystallization, leading to the change of the coordination number of Mn2+. Correspondingly, the luminescence changes from red to bright green and finally back to red emission. By fabricating a test‐paper containing CsMnCl3(H2O)2, DMAC and DMF can be detected quickly with a response time of less than one minute. These results can expand potential applications for low‐dimensional lead‐free perovskites.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Zhang X., Zhao Y., Wei Y., Qiu L., Wang W., Wang Z., Yang H., Chen K., Molokeev M. S., Li G.
Заглавие : A highly selective and rapid solvatochromic material for amide solvent detection
Место публикации : Chem. Commun. - 2022. - Vol. 58, Is. 85. - P.11953-11956. - ISSN 1364548X (ISSN), DOI 10.1039/d2cc04566d
Примечания : Cited References: 24. - This work was supported by the National Natural Science Foundation of China (Grant No. 52072349), the Natural Science Foundation of Zhejiang Province (No. LR22E020004 and LZ22A040005), the State Key Laboratory of Silicate Materials for Architectures (Wuhan University of Technology) (No. SYSJJ2022-11), and the State Key Laboratory of Advanced Technology for Materials Synthesis and Processing (Wuhan
Аннотация: The detection of amide solvents is essential to human health due to their carcinogenicity. A simple, solvatochromic luminescent material is presented for quick and accurate detection of amides. The luminescence color variation from blue to yellow is ascribed to the amide-induced phase transformation from Cs2ZnBr4:Cu to CsBr:Cu+/Cu2+.
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Вид документа : Статья из сборника (однотомник)
Шифр издания :
Автор(ы) : Гудим, Ирина Анатольевна, Еремин, Евгений Владимирович, Титова, Вероника Романовна
Заглавие : Влияние компонентов растворителя на рост кристаллов тригональных оксиборатов со структурой хантита
Коллективы : Байкальская международная конференция "Магнитные материалы. Новые технологии", "Магнитные материалы. Новые технологии", Байкальская международная конференция, "Magnetic materials. New tecnologies", Baikal International Conference, Иркутский государственный университет
Место публикации : Магнитные материалы. Новые технологии: тез. докл. IX Байкал. междунар. конф. BICMM-2023/ чл. прогр. ком.: S. S. Aplesnin [et al.] ; чл. орг. ком. R. S. Iskhakov [et al.]. - Иркутск, 2023. - С. 155-156. - ISBN 978-5-962402178-0, DOI 10.26516/978-5-9624-2178-0.2023.1-207
Примечания : Библиогр.: 3
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