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Laser photolysis of fluorone dyes in a chitosan matrix / E. A. Slyusareva [et al.] // Quantum Electron. - 2012. - Vol. 42, Is. 8. - P. 687-692, DOI 10.1070/QE2012v042n08ABEH014860. - Cited References: 32 . - ISSN 1063-7818

РУБ Engineering, Electrical & Electronic + Physics, Applied
Рубрики:
POLY(VINYL ALCOHOL) MATRIX
   XANTHENE DYES
   ROSE-BENGAL
   FLUORESCENCE PROPERTIES
   DELAYED FLUORESCENCE
   ORGANIC-MOLECULES
   TRIPLET-STATE
   EXCITATION
   ABSORPTION
   PHOSPHORESCENCE
Кл.слова (ненормированные):
laser photolysis -- fluorescein -- dibromofluorescein -- eosin Y -- erythrosin B -- Rose Bengal -- chitosan -- photobleaching kinetics -- two-step absorption
Аннотация: Kinetics of laser-induced photobleaching of fluorone dyes (fluorescein, dibromofluorescein, eosin Y, erythrosin B, Rose Bengal) is studied in a chitosan matrix. For all dyes the bleaching kinetics at the intensities of laser radiation 0.7 — 11.9 W cm-2 demonstrates quasi-monomolecular behaviour. The results are analysed using a kinetic model, based on the four-level (S0, S1, T1, Tn) scheme of the dye with chemically active triplet states taken into account. It is shown that the rate constants of the chemical reaction involving higher triplet states in the dyes studied amount to (3.9 — 18.6) × 106 s-1 and exceed the analogous values for the reaction involving the first lower triplet states by nine orders of magnitude. The rate of reaction involving the first triplet states appeared to be higher by one — two orders of magnitude than that in the case of higher triplet states involved because of low population of the latter. The possible mechanism of dye bleaching with participation of chitosan that consists in reduction of the dye to the leuco form by transfer of hydrogen from the chitosan matrix is discussed.

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Публикация на русском языке Лазерный фотолиз флуороновых красителей в хитозановой матрице [Текст] / Е. А. Слюсарева [и др.] // Квант. электроника : Физический институт им. П.Н.Лебедева РАН, 2012. - Т. 42 № 8. - С. 687-692

Держатели документа:
[Slyusareva, E. A.
Sizykh, A. G.
Gerasimova, M. A.
Slabko, V. V.] Siberian Fed Univ, Krasnoyarsk 660041, Russia
[Myslivets, S. A.] Russian Acad Sci, Siberian Branch, LV Kirensky Phys Inst, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Slyusareva, E. A.; Sizykh, A. G.; Gerasimova, M. A.; Slabko, V. V.; Слабко, Виталий Васильевич; Myslivets, S. A.; Мысливец, Сергей Александрович
}
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The effect of halogen substitution on the structure and electronic spectra of fluorone dyes / E. A. Slyusareva [et al.] // Opt. Spectrosc. - 2012. - Vol. 112, Is. 5. - P. 671-678, DOI 10.1134/S0030400X12040194. - Cited References: 44. - This work was supported by the FTsP Kadry GK-P333 and by the Siberian Branch of the Russian Academy of Sciences (Integration project no. 2). We are grateful to the Joint Supercomputer Center of the Russian Academy of Sciences (Moscow) and to the Complex of High-Performance Computations of the IKIT of Siberian Federal University. E. A. Slyusareva acknowledges support from the German Academic Exchange Service and the Ministry of Education and Science of the Russian Federation (the program "Mikhail Lomonosov II") of scientific research at the University of Regensburg and in the Helmholtz Center in Berlin (Germany). . - ISSN 0030-400X

РУБ Optics + Spectroscopy
Рубрики:
POLARIZABLE CONTINUUM MODEL
   BORIC-ACID GLASS
   XANTHENE DYES
   FLUORESCEIN DERIVATIVES
   DELAYED FLUORESCENCE
   EOSIN-Y
   ABSORPTION
   PHOSPHORESCENCE
   TRANSITIONS
   EXCITATION
Аннотация: By means of the B3LYP density functional method with the use of the polarized continuum model PCM, we have performed quantum-chemical computations of the electronic absorption and fluorescence spectra of fluorone dianions: fluorescein, dibromofluorescein, eosin, erythrosine, and Rose Bengal in vacuum and methanol. We have revealed conformational features of the structure of fluorone dianions (charge redistribution, changes in the bond lengths and angles between bonds) second by the halogen substitution, the transition from the ground state to an excited state, and the change of the solvent (vacuum-methanol). Absorption and fluorescence wavelengths, constant dipole moments, transition dipole moments, and oscillator strengths have been calculated. We have showed that, upon halogenation of fluorones, the absorption spectra are redshifted and the Stokes shift decreases, which is qualitatively consistent with experimental results.

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Публикация на русском языке Влияние галогензамещения на структуру и электронные спектры флуороновых красителей [Текст] / Е. А. Слюсарева [и др.] // Оптика и спектроскопия : Наука, 2012. - Т. 112 № 5. - С. 729-737

Держатели документа:
[Slyusareva, E. A.
Tomilin, F. N.
Sizykh, A. G.
Tankevich, E. Yu.
Kuzubov, A. A.
Ovchinnikov, S. G.] Siberian Fed Univ, Krasnoyarsk 660041, Russia
[Tomilin, F. N.
Ovchinnikov, S. G.] Russian Acad Sci, Siberian Branch, Kirensky Inst Phys, Krasnoyarsk 660036, Russia

Доп.точки доступа:
Slyusareva, E. A.; Tomilin, F. N.; Томилин, Феликс Николаевич; Sizykh, A. G.; Tankevich, E. Y.; Kuzubov, A. A.; Кузубов, Александр Александрович; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич
}
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Aver'yanov, E. M.
Manifestations of the higher moments of the orientation distribution function of molecules in the spectral properties of an impurity nematic / E. M. Aver'yanov, V. G. Rumyantsev // J. Exp. Theor. Phys. - 2004. - Vol. 98, Is. 6. - P. 1146-1151, DOI 10.1134/1.1777627. - Cited References: 15 . - ISSN 1063-7761

РУБ Physics, Multidisciplinary
Рубрики:
LIQUID-CRYSTAL
   SCATTERING
   PHASES
   MATRIX
   ORDER
   DYES
Кл.слова (ненормированные):
Absorption -- Band structure -- Impurities -- Molecular dynamics -- Polarization -- Spectrum analysis -- Distribution function -- Local field parameters -- Splitting -- Temperature dependence -- Nematic liquid crystals
Аннотация: The polarized electronic absorption spectra, orientation ordering, and the special local field features were studied for push-pull linear dye molecules with strong donor-acceptor electronic conjugation of terminal fragments in the matrix of a nematic liquid crystal. The temperature-induced inversion of the sign of the splitting of polarized impurity absorption bands was observed. This effect was shown to be caused by the statistical character of orientation ordering of impurity molecules and manifestation of the higher moments of the orientation distribution function. The dependence of local field parameters (Lorentz tensor components) of impurity molecules on their orientation ordering was established. This dependence was used to reproduce the temperature dependence of the orientation order parameter of the matrix. (C) 2004 MAIK "Nauka / Interperiodica".

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Держатели документа:
Russian Acad Sci, LV Kirensky Phys Inst, Siberian Div, Krasnoyarsk 660036, Russia
Res Inst Organ Intermediates & Dyes, Dolgoprudnyi 141700, Moscow Oblast, Russia
ИФ СО РАН
Kirenskii Institute of Physics, Siberian Division, Russian Academy of Sciences, Akademgorodok, Krasnoyarsk, 660036, Russian Federation
Research Institute of Organic Intermediates and Dyes, Dolgoprudnyi, Moscow oblast, 141700, Russian Federation

Доп.точки доступа:
Rumyantsev, V. G.; Аверьянов, Евгений Михайлович
}
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Nonlinear optical frequency-mixing in DYE vapors / V. F. Lukinykh [et al.] // APPLIED PHYSICS B-PHOTOPHYSICS AND LASER CHEMISTRY. - 1985. - Vol. 38, Is. 2. - P. 143-146, DOI 10.1007/BF00697454. - Cited References: 18 . - ISSN 0721-7269

РУБ Physics, Applied

Кл.слова (ненормированные):
42.65 -- 42.80 -- DYES AND DYEING -- LASERS, SOLID STATE - Applications -- DYE VAPORS -- NONLINEAR OPTICAL FREQUENCY-MIXING -- LIGHT

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Держатели документа:
L. V. Kirensky Institute of Physics, USSR Academy of Sciences, Siberian Branch and Krasnoyarsk University, Krasnoyarsk, SU-660036, Russia

Доп.точки доступа:
Lukinykh, V. F.; Myslivets, S. A.; Мысливец, Сергей Александрович; Popov, A. K.; Попов, Александр Кузьмич; Slabko, V. V.; Слабко, Виталий Васильевич
}
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AVERYANOV, E. M.
STATIONARY SPECTRUM OF ADMIXED LIQUID-CRYSTAL POLARIZED FLUORESCENCE / E. M. AVERYANOV // Zhurnal Eksperimentalnoi Teor. Fiz. - 1994. - Vol. 106, Is. 3. - P. 767-779. - Cited References: 29 . - ISSN 0044-4510

РУБ Physics, Multidisciplinary
Рубрики:
LOCAL FIELD
   SPECTROSCOPY
   PARAMETERS
   DYES

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AVERYANOV, E. M.
POLARIZED LUMINESCENCE SPECTRUM OF IMPURITY LIQUID-CRYSTAL - THE DEGENERATION LIFTED AND RENEWED BY RELAXATION / E. M. AVERYANOV // Zhurnal Eksperimentalnoi Teor. Fiz. - 1993. - Vol. 103, Is. 6. - P. 2018-2038. - Cited References: 45 . - ISSN 0044-4510

РУБ Physics, Multidisciplinary
Рубрики:
RESOLVED FLUORESCENCE DEPOLARIZATION
   UNIAXIAL MOLECULAR SAMPLES
   NEMATIC ORDER PARAMETERS
   EXCITED-STATES
   SPECTROSCOPY
   MEMBRANES
   FLUOROPHORES
   ORIENTATION
   TRANSITION
   DYES
Аннотация: The general molecular-statistical approach is proposed for the analysis or the polarized luminescence spectrum for impurity molecule of an arbitrary symmetry in the nematic liquid crystal matrix. On the particular example of uniaxial molecules the influence of features of the molecular electron structure, orientational statistics, molecular dynamics, and features of the anisotropic intermolecular coupling upon the positions of maxima v(if)(t) of impurity fluorescence polarized bands J(ij)(t) is studied. For the first time it is shown that all these factors significantly affect the degree of spectrum v(ij)(t) degeneration. For t not-equal 0, relaxation of excited impurity molecule subsystem toward the orientational distribution lifts a partial degeneration of spectrum v(ij), occuring at t not-equal 0, and renews partial or total degeneration of spectrum v(ij) in the limit t = infinity. In the lack of the spectrum v(ij) degeneration for t = 0 the relaxation may restore partial degeneration for t not-equal 0 as a function of the features of electron structure of molecules. The results of work explain the familiar experimental data on the number of independent component v(ij) and relation between them, on dependence of v(ij) upon the order of matrix and impurity subsystem, on the mutual relation in the positions of impurity band polarized component in the absorption and fluorescence spectra.

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    Synthesis, luminescent properties and theoretical calculations of novel orange-red-emitting Ca2Y8(SiO4)6O2:Sm3+ phosphors for white light-emitting diodes / C. -T. Chen [et al.] // Dyes Pigm. - 2018. - Vol. 150. - P. 121-129, DOI 10.1016/j.dyepig.2017.10.047. - Cited References: 61. - This research was supported by Minister of Science and Technology under contract no. MOST 105-2622-E-033-003-CC2 and MOST 104-2628-E-033-002-MY3. . - ISSN 0143-7208
   Перевод заглавия: Синтез, люминесцентные свойства и теоретические вычисления нового оранжево-красного люминофора Ca2Y8(SiO4)6O2:Sm3+ для белых светодиодов
Кл.слова (ненормированные):
Ca2Y8(SiO4)6O2 -- Photoluminescence -- Phosphor -- Solid state reaction
Аннотация: The novel orange-red-emitting Ca2Y8(SiO4)6O2:Sm3+ phosphors (CYSO:Sm3+) were synthesized via conventional a solid state reaction. The crystal structure and atomic coordinates of CYSO:Sm3+ was characterized by Rietveld refinement. Luminesce properties of as-synthesized CYSO:Sm3+ phosphors are carried out by PL/PLE, decay life time, thermal quenching as well as reflectance spectrometer and LED fabrications. The results indicates that composition-optimized CYSO:1%Sm3+ exhibits orange-red emission peaks located on 564, 601, 608 and 648 nm attributed to the transitions of 4G5/2 → 6H5/2, 4G5/2 → 6H7/2, 4G5/2 → 6H7/2 and 4G5/2 → 6H9/2, respectively. The decay lifetime of CYSO:Sm3+ phosphors was in the range of 0.37–1.10 ms. The temperature-dependent photoluminescence is decreased to 80% from room temperature to 150 °C, which is superior to that of commercial red phsophpr-Y2O3:Eu3+. The results of LED fabrication by combing 405 chips and blue/green phosphors are demonstrated in this study. Finally, from viewpoint of theoretical calculations, band structure and density of state for CYSO and CYSO:Sm3+ are studied by first principles calculations. All the results indicate that CYSO:Sm3+ phosphors could be a potential material for white light-emitting diodes.

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Держатели документа:
Department of Chemical Engineering, Chung Yuan Christian University, Chung Li, Taiwan
National Chung Shan Institute of Science & Technology, Taoyuan, Taiwan
Laboratory of Crystal Physics, Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Krasnoyarsk, Russian Federation
Department of Physics, Far Eastern State Transport University, Khabarovsk, Russian Federation
Siberian Federal University, Krasnoyarsk, Russian Federation

Доп.точки доступа:
Chen, C. -T.; Lin, T. -J.; Molokeev, M. S.; Молокеев, Максим Сергеевич; Liu, W. -R.
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Fluorescence and photoinduced proton transfer in the protolytic forms of fluorescein: Experimental and computational study / M. A. Gerasimova [et al.] // Dyes Pigm. - 2020. - Vol. 173. - Ст. 107851, DOI 10.1016/j.dyepig.2019.107851. - Cited References: 58. - This work is supported by the Russian Foundation for Basic Research, Russia (project 19-02-00450 ). S.A.V. thanks the National Science Foundation, United States for financial support through a CAREER Award ( CHE-1654547 ). . - ISSN 0143-7208
Кл.слова (ненормированные):
Fluorescein protolytic forms -- Absorption -- Fluorescence -- TD-DFT -- Proton transfer -- Excited-state dissociation constant
Аннотация: In contrast to the well-studied absorption spectra of different protolytic forms of fluorescein, the complex structure of the fluorescence spectra in a wide pH range is not completely understood because of the interplay between emission and photoinduced proton transfer in the electronic excited states. We provide insight into this interplay through a combined analysis of the experimental data, obtained by absorption and steady-state fluorescence spectroscopy at pH 0.3–10.5, and the time-dependent density functional theory (TD-DFT). The TD-DFT based computational model is validated on dianion and used to model the spectra of other protolytic forms. The protolytic/tautomeric forms of fluorescein are classified according to the partial charges on the triple chromophore ring, and electronic transitions are analyzed in terms of changes in molecular geometries and orbitals. A linear regression analysis between the calculated and experimental results based on both absorption and well-understood dianionic and cationic fluorescence peaks is used to assign the monoanionic (496 nm), neutral quinoid (550 nm) and neutral zwitterionic (483 nm) fluorescence peaks, whose positions were not clear prior to this work. The values of the excited-state dissociation microconstants pka* for different forms of fluorescein are calculated by means of the Forster cycle in conjunction with the spectroscopic measurements and computational data.

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Держатели документа:
Siberian Federal University, Svobodny Prospect 79, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Federal Research Center KSC SB RAS, Akademgorodok 50/38, Krasnoyarsk, 660036, Russian Federation
Department of Chemistry, University of Nevada, Reno, North Virginia Street 1664, Reno, NV 89557-0216, United States
Research Center for Computational Design of Advanced Functional Materials, National Institute of Advanced Industrial Science and Technology, Central 2, Umezono 1-1-1, Tsukuba, 305-8568, Japan

Доп.точки доступа:
Gerasimova, M. A.; Tomilin, F. N.; Томилин, Феликс Николаевич; Malyar, E. Y.; Varganov, S. A.; Fedorov, D. G.; Ovchinnikov, S. G.; Овчинников, Сергей Геннадьевич; Slyusareva, E. A.
}
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Solvent effect in the theoretical absorption and emission spectra of fluorescein dyes / F. N. Tomilin, A. V. Rogova, E. V. Kaufman [et al.] // 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. - Cited References: 13. - This work was supported by the Russian Foundation for Basic Research, project 19-02-00450
Кл.слова (ненормированные):
fluorescein -- eosin Y -- erythrosin B -- dianion -- PCM -- time-dependent density functional theory
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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Держатели документа:
Siberian Federal University, Svobodny Prospect 79, Krasnoyarsk, 660041, Russian Federation
Kirensky Institute of Physics, Krasnoyarsk Scientific Center, Siberian Branch, Russian Academy of Sciences, Akademgorodok 50, bld. 38, Krasnoyarsk, 660036, Russian Federation

Доп.точки доступа:
Tomilin, F. N.; Томилин, Феликс Николаевич; Rogova, A. V.; Kaufman, E. V.; Drevolsky, A. S.; Gerasimova, M. A.; Slyusareva, E. A.; International Conference on Pulsed Lasers and Laser Applications(14 ; 2019 ; 15-20 Sept. ; Tomsk)
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10.

    Carbon double coated Fe3O4@C@C nanoparticles: Morphology features, magnetic properties, dye adsorption / C. R. Lin, O. S. Ivanova, I. S. Edelman [et al.] // Nanomaterials. - 2022. - Vol. 12, Is. 3. - Ст. 376, DOI 10.3390/nano12030376. - Cited References: 44. - The work was supported financially by the Russian Foundation for Basic Research, Grant No. 19-52-52002 and Ministry of Science and Technology of Taiwan, Grants MOST No. 108-2923-M-153-001-MY3 and No. 109-2112-M-153-003-. The support was obtained also from the Joint Scientific Center of the Siberian Federal University supported by the State assignment (#FSRZ-2020-0011) of the Ministry of Science and Higher Education of the Russian Federation, where the Transmission Electron Microscopy studies were carried out . - ISSN 2079-4991
   Перевод заглавия: Наночастицы Fe3O4@C@C с двойным углеродным покрытием: Морфологические особенности, магнитные свойства, адсорбция красителей

РУБ Chemistry, Multidisciplinary + Nanoscience & Nanotechnology + Materials Science, Multidisciplinary + Physics, Applied
Рубрики:
SOLID-PHASE EXTRACTION
FE3O4 NANOPARTICLES
PROFILE REFINEMENT
Кл.слова (ненормированные):
core-shell Fe3O4@C nanoparticles -- core-shell Fe3O4@C@C nanoparticles -- magnetic properties -- dyes adsorption
Аннотация: This work is devoted to the study of magnetic Fe3O4 nanoparticles doubly coated with carbon. First, Fe3O4@C nanoparticles were synthesized by thermal decomposition. Then these synthesized nanoparticles, 20–30 nm in size were processed in a solution of glucose at 200 °C during 12 h, which led to an unexpected phenomenon – the nanoparticles self-assembled into large conglomerates of a regular shape of about 300 nm in size. The morphology and features of the magnetic properties of the obtained hybrid nanoparticles were characterized by transmission electron microscopy, differential thermo-gravimetric analysis, vibrating sample magnetometer, magnetic circular dichroism and Mössbauer spectroscopy. It was shown that the magnetic core of Fe3O4@C nanoparticles was nano-crystalline, corresponding to the Fe3O4 phase. The Fe3O4@C@C nanoparticles presumably contain Fe3O4 phase (80%) with admixture of maghemite (20%), the thickness of the carbon shell in the first case was of about 2–4 nm. The formation of very large nanoparticle conglomerates with a linear size up to 300 nm and of the same regular shape is a remarkable peculiarity of the Fe3O4@C@C nanoparticles. Adsorption of organic dyes from water by the studied nanoparticles was also studied. The best candidates for the removal of dyes were Fe3O4@C@C nanoparticles. The kinetic data showed that the adsorption processes were associated with the pseudo-second order mechanism for cationic dye methylene blue (MB) and anionic dye Congo red (CR). The equilibrium data were more consistent with the Langmuir isotherm and were perfectly described by the Langmuir–Freundlich model.

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Держатели документа:
Natl Pingtung Univ, Dept Appl Phys, Pingtung City 90003, Taiwan.
RAS, FRC KSC SB, Kirensky Inst Phys, Krasnoyarsk 660036, Russia.
Siberian Fed Univ, Inst Engn Phys & Radioelect, Krasnoyarsk 660041, Russia.
RAS, FRC KSC SB, Inst Chem & Chem Technol, Krasnoyarsk 660036, Russia.

Доп.точки доступа:
Lin, Chun-Rong; Ivanova, O. S.; Иванова, Оксана Станиславовна; Edelman, I. S.; Эдельман, Ирина Самсоновна; Knyazev, Yu. V.; Князев, Юрий Владимирович; Zharkov, S. M.; Жарков, Сергей Михайлович; Petrov, D. A.; Петров, Дмитрий Анатольевич; Sokolov, A. Е.; Соколов, Алексей Эдуардович; Svetlitsky, E. S.; Светлицкий, Евгений Сергеевич; Velikanov, D. A.; Великанов, Дмитрий Анатольевич; Solovyov, Leonid A.; Chen, Ying-Zhen; Tseng, Yaw-Teng; Russian Foundation for Basic ResearchRussian Foundation for Basic Research (RFBR) [19-52-52002]; Ministry of Science and Technology of TaiwanMinistry of Science and Technology, Taiwan [108-2923-M-153-001-MY3, 109-2112-M-153-003]; Joint Scientific Center of the Siberian Federal University [FSRZ-2020-0011]; Ministry of Science and Higher Education of the Russian Federation
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