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1.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Antipina L. Yu., Tomilin F. N., Vysotski E. S., Ovchinnikov S. G.
Заглавие
: A quantum chemical study of the formation of 2-hydroperoxy-coelenterazine in the Сa2+-regulated photoprotein obelin
Место публикации
: J. Struct. Chem.: Springer, 2011. - Vol. 52, Is. 5. - P.870-875. - ISSN 0022-4766
Примечания
: Cited References: 19. - The work was supported by RFBR (07-04-00930-a), the "Molecular and Cell Biology" Program of the Presidium of the Russian Academy of Sciences, and the Program of the Siberian Division of the Russian Academy of Sciences (project No. 2) within the implementation of the Federal Targeted Program "Scientific and Scientific Pedagogical Personnel of Innovative Russia, 2010" (P333 and P213).
Предметные рубрики:
CALCIUM-DISCHARGED OBELIN
SEMIEMPIRICAL METHODS
1.7 ANGSTROM
OPTIMIZATION
PARAMETERS
MECHANISM
FLUORESCENCE
ELEMENTS
PROTEIN
EMITTER
Ключевые слова
(''Своб.индексиров.''): coelenterazine--2-hydroperoxy-coelenterazine--obelia longissima--renilla muelleri
Аннотация:
The Ca2+-regulated photoprotein obelin determines the luminescence of the marine hydroid Obelia longissima. Bioluminescence is initiated by calcium and appears as a result of the oxidative decarboxylation related to the coelenterazine substrate. The luciferase of the luminescent marine coral Renilla muelleri (RM) also uses coelenterazine as a substrate. However, three proteins are involved in the in vivo bioluminescence of these animals: luciferase, green fluorescent protein, and Ca2+-regulated coelenterazine-binding protein (CBP). In fact, CBP that contains one strongly bound coelenterazine molecule is the RM luciferase substrate in the in vivo bioluminescent reaction. Coelenterazine becomes available for oxygen and the reaction with luciferase only after binding CBP with calcium ions. Unlike Ca2+-regulated photoproteins, the coelenterazine molecule is not activated by oxygen in the CBP molecule. In this work, by means of quantum chemical methods the behavior of substrates in these proteins is analyzed. It is shown that coelenterazine can form different tautomers: CLZ(2H) and CLZ(7H). The formation of 2-hydroperoxy-coelenterazine is studied. According to the obtained data, these proteins use different forms of the substrates for the reaction. In obelin, the substrate is in the CLZ(2H) form that affords hydrogen peroxide. In RM, coelenterazine is in the CLZ(7H) form, and therefore, CBP is not activated by oxygen.
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2.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Slyusareva E. A., Sizykh A. G., Gerasimova M. A., Slabko V. V., Myslivets S. A.
Заглавие
: Laser photolysis of fluorone dyes in a chitosan matrix
Место публикации
: Quantum Electron.: Turpion LTD, 2012. - Vol. 42, Is. 8. - P.687-692. - ISSN 1063-7818,
DOI
10.1070/QE2012v042n08ABEH014860
Примечания
: Cited References: 32
Предметные рубрики:
POLY(VINYL ALCOHOL) MATRIX
XANTHENE DYES
ROSE-BENGAL
FLUORESCENCE
PROPERTIES
DELAYED
FLUORESCENCE
ORGANIC-MOLECULES
TRIPLET-STATE
EXCITATION
ABSORPTION
PHOSPHORESCENCE
Ключевые слова
(''Своб.индексиров.''): 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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3.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Slyusareva E. A., Tomilin F. N., Sizykh A. G., Tankevich E. Y., Kuzubov A. A., Ovchinnikov S. G.
Заглавие
: The effect of halogen substitution on the structure and electronic spectra of fluorone dyes
Место публикации
: Opt. Spectrosc.: MAIK NAUKA/INTERPERIODICA/SPRINGER, 2012. - Vol. 112, Is. 5. - P.671-678. - ISSN 0030-400X,
DOI
10.1134/S0030400X12040194
Примечания
: 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).
Предметные 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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4.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Chen M., Xia Z., Molokeev M. S., Liu Q.
Заглавие
: Insights into Ba4Si6O16 structure and photoluminescence tuning of Ba4Si6O16:Ce3+,Eu2+ phosphors
Место публикации
: J. Mater. Chem. C: Royal Society of Chemistry, 2015. - Vol. 3, Is. 48. - P.12477-12483. - ISSN 20507534 (ISSN),
DOI
10.1039/c5tc03271g
Примечания
: Cited References: 39. - This work was supported by the National Natural Science Foundations of China (Grant No. 51572023 and 51272242), Natural Science Foundations of Beijing (2132050), the Program for New Century Excellent Talents in University of Ministry of Education of China (NCET-12-0950), Beijing Nova Program (Z131103000413047), the Funds of the State Key Laboratory of New Ceramics and Fine Processing, Tsinghua University (KF201306), and Fundamental Research Funds for the Central Universities (FRF-TP-14-005A1).
Предметные рубрики:
LIGHT-EMITTING-DIODES
ENERGY-TRANSFER
LUMINESCENCE PROPERTIES
WHITE-LIGHT
GLASS-CERAMICS
BA PHOSPHORS
EMISSION
GREEN
EU2+
FLUORESCENCE
Аннотация:
The versatile polymorphism and chemical compositions of barium silicates have been studied for a long time and their crystal structures have been established. Herein, we focused on the understanding of the crystal structure of the Ba4Si6O16 phase and the structural correlation of Ba4Si6O16 and Ba2Si3O8; moreover, the luminescence properties of Ce3+,Eu2+-co-activated Ba4Si6O16 phosphors have been discussed. Ba4Si6O16:Ce3+,Eu2+ phosphors show tunable blue-green emission upon excitation with 365 nm ultraviolet (UV) light. The blue emission originates from Ce3+, whereas the bluish-green emission is ascribed to Eu2+, and variation in the emission peak wavelength from 442 to 497 nm can be achieved by properly tuning the Ce3+/Eu2+ ratio. Energy transfer from Ce3+ to Eu2+ in the Ba4Si6O16 host has been validated by the variation of emission spectra as well as the variation of Ce3+ decay lifetimes with increasing Eu2+ concentration, and the energy transfer mechanism is demonstrated to be a resonant type via a dipole-dipole process. The results suggest that Ba4Si6O16:Ce3+,Eu2+ phosphors are potential candidates as a blue-green component for UV-excited white light-emitting diodes. © 2015 The Royal Society of Chemistry.
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5.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Edelman I. S., Sokolov A. E., Zabluda V. N., Shubin A. A., Martyanov O. N.
Заглавие
: Magnetic circular dichroism analysis of crude oil
Коллективы
: Russian Federation [NSh-2886.2014.2]; Kirensky Institute of Physics (Siberian Branch, Russian Academy of Sciences) [V.44.1.15]; Boreskov Institute of Catalysis (Siberian Branch, Russian Academy of Sciences) [V.44.1.15]
Место публикации
: J. Struct. Chem.: MAIK Nauka-Interperiodica / Springer, 2016. - Vol. 57, Is. 2. - P.382-389. - ISSN 0022-4766,
DOI
10.1134/S0022476616020207. - ISSN 1573-8779(eISSN)
Примечания
: Cited References:33. - The work was carried out with the partial support of the grant of the President of the Russian Federation (NSh-2886.2014.2), and in the frameworks of the base budget financing of Kirensky Institute of Physics and Boreskov Institute of Catalysis (Siberian Branch, Russian Academy of Sciences) (V.44.1.15.).
Предметные рубрики:
Near-UV/visible spectroscopy
Electron-spin-resonance
Asphaltene dispersions
Single-crystals
Absorption
VO2+
EPR
FLuorescence
Aggregation
Absorbency
Ключевые слова
(''Своб.индексиров.''): magnetic circular dichroism (mcd)--mcd spectroscopy--absorption spectroscopy of oil
Аннотация:
Optical and magneto-optical properties of solutions of crude oil of different origin (i.e., taken from different fields) are studied in the visible and near-UV region of optical emission. Magnetic circular dichroism (MCD) spectra of oil are obtained in the vicinity of wavelengths of ~410 nm, 533 nm, and 576 nm. It is demonstrated that the intensity of the MCD signal depends on the origin of crude oil, and it is proportional to the oil concentration in the solution. The comparison of the magneto-optical spectroscopy data with the chemical composition of samples allows us to conclude that the observed magneto-optical activity is determined by the presence of VO2+ complexes in the oil samples studied. The revealed magneto-optical activity of conventional oil can form a basis of a new method for the analysis of the composition and properties of oil of different origin.
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6.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Alieva R. R., Tomilin F. N., Kuzubov A. A., Ovchinnikov S. G., Kudryasheva N. S.
Заглавие
: Ultraviolet
fluorescence
of coelenteramide and coelenteramide-containing fluorescent proteins. Experimental and theoretical study
Место публикации
: J. Photochem. Photobiol. B Biol.: Elsevier, 2016. - Vol. 162. - P.318-323. - ISSN 10111344 (ISSN),
DOI
10.1016/j.jphotobiol.2016.07.004
Примечания
: Cited References: 49. - This work was supported by the state budget allocated to the fundamental research at the Russian Academy of Sciences (project No 01201351504); the Russian Foundation for Basic Research, Grant No 15-43-04377-sibir; and Russian president's grant NSh-7559.2016.2.
Предметные рубрики:
DENSITY-FUNCTIONAL THEORY
ELECTRON-EXCITED-STATES
PHOTOPROTEIN OBELIN
DISCHARGED-OBELIN
LIGHT-EMITTERS
BIOLUMINESCENCE
AEQUORIN
LUMINESCENCE
MECHANISM
CHEMILUMINESCENCE
Ключевые слова
(''Своб.индексиров.''): coelenteramide--fluorescent protein--discharged photoproteins--obelin--aequorin--
fluorescence
--excitation energy--
fluorescence
--b3lyp
Аннотация:
Coelenteramide-containing fluorescent proteins are products of bioluminescent reactions of marine coelenterates. They are called ‘discharged photoproteins’. Their light-induced
fluorescence
spectra are variable, depending considerably on external conditions. Current work studies a dependence of light-induced
fluorescence
spectra of discharged photoproteins obelin, aequorin, and clytin on excitation energy. It was demonstrated that photoexcitation to the upper electron-excited states (260–300 nm) of the discharged photoproteins initiates a
fluorescence
peak in the near UV region, in addition to the blue-green emission. To characterize the UV
fluorescence
, the light-induced
fluorescence
spectra of coelenteramide (CLM), fluorophore of the discharged photoproteins, were studied in methanol solution. Similar to photoproteins, the CLM spectra depended on photoexcitation energy; the additional peak (330 nm) in the near UV region was observed in CLM
fluorescence
at higher excitation energy (260–300 nm). Quantum chemical calculations by time depending method with B3LYP/cc-pVDZ showed that the conjugated pyrazine-phenolic fragment and benzene moiety of CLM molecule are responsible for the additional UV
fluorescence
peak. Quantum yields of CLM
fluorescence
in methanol were 0.028 ± 0.005 at 270–340 nm photoexcitation. A conclusion was made that the UV emission of CLM might contribute to the UV
fluorescence
of the discharged photoproteins. The study develops knowledge on internal energy transfer in biological structures – complexes of proteins with low-weight aromatic molecules. © 2016 Elsevier B.V.
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7.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Malakhovskii A. V., Sokolov A. E., Temerov V. L., Bezmaternykh L. N., Sukhachev A. L., Seredkin V. A., Gnatchenko S. L., Kachur I. S., Piryatinskaya V. G.
Заглавие
: Polarized absorption spectra and spectroscopic parameters of Tm3+ in the TmAl3(BO3)(4) single crystal
Разночтения заглавия
:авие SCOPUS: Polarized absorption spectra and spectroscopic parameters of Tm 3+ in the TmAl3(BO3)4 single crystal
Место публикации
: Phys. Solid State: MAIK NAUKA/INTERPERIODICA/SPRINGER, 2008. - Vol. 50, Is. 7. - P1287-1293. - ISSN 1063-7834,
DOI
10.1134/S1063783408070159
Примечания
: Cited References: 36
Предметные рубрики:
RARE-EARTH IONS
ELECTRONIC ENERGY LEVELS
DIODE-PUMPED LASER
OPTICAL-ABSORPTION
ALUMINUM GARNET
MU-M
INTENSITIES
FLUORESCENCE
GLASSES
OXIDE
Аннотация:
High-optical-quality single crystals of the TmAl3(BO3)(4) compound were synthesized from a solution in the melt. The absorption spectra in the sigma and pi polarizations for the H-3(6) - F-3(4), H-3(6) - H-3(5), H-3(6) - H-3(4), H-3(6) - F-3(3), H-3(6) - F-3(2), H-3(6) - (1)G(4), and H-3(6) - D-1(2) transitions in the Tm3+ ion were recorded at room temperature. The transition intensities were analyzed in the framework of the Judd-Ofelt theory generalized to the case of anisotropic crystals, and the following parameters of the theory were obtained: Omega(2) = 6.14 x 10(-20) cm(2), Omega(4) = 3.09 x 10(-20) cm(2), and Omega(6) = 2.04 x 10(-20) cm(2). The lifetimes and the branching ratios were determined for all possible transitions.
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8.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: AVERYANOV E. M.
Заглавие
: STATIONARY SPECTRUM OF ADMIXED LIQUID-CRYSTAL POLARIZED
FLUORESCENCE
Место публикации
: Zhurnal Eksperimentalnoi Teor. Fiz.: MEZHDUNARODNAYA KNIGA, 1994. - Vol. 106, Is. 3. - P767-779. - ISSN 0044-4510
Примечания
: Cited References: 29
Предметные рубрики:
LOCAL FIELD
SPECTROSCOPY
PARAMETERS
DYES
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9.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Averyanov E. M.
Заглавие
: Splitting of polarized impurity
fluorescence
bands in the steady-state spectrum of an isotropic solution
Место публикации
: JETP Letters. - 1994. - Vol. 59, Is. 1. - P.23-26. - ISSN 0021-3640
Примечания
: Cited References: 12
Предметные рубрики:
RELAXATION
Аннотация:
A difference is predicted between the peaks, nu(VV) and nu(VH), Of the polarized components J(VV)(nu) and J(VH)(nu) in the steady-state spectrum of impurity
fluorescence
in an isotropic solution. This difference would result from a temporal correlation between an orientational Brownian diffusion of excited fluorescing molecules and a structural relaxation of the surrounding matrix molecules.
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10.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: AVERYANOV E. M.
Заглавие
: POLARIZED LUMINESCENCE SPECTRUM OF IMPURITY LIQUID-CRYSTAL - THE DEGENERATION LIFTED AND RENEWED BY RELAXATION
Место публикации
: Zhurnal Eksperimentalnoi Teor. Fiz.: MEZHDUNARODNAYA KNIGA, 1993. - Vol. 103, Is. 6. - P2018-2038. - ISSN 0044-4510
Примечания
: Cited References: 45
Предметные 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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11.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Averyanov E. M., Gunyakov V. A.
Заглавие
: New features in the structural relaxation of a nematic liquid-crystal doped with luminescent impurity molecules
Место публикации
: JETP Letters. - 1993. - Vol. 57, Is. 8. - P.492-496. - ISSN 0021-3640
Примечания
: Cited References: 15
Предметные рубрики:
FLUORESCENCE
DEPOLARIZATION
ORIENTATIONAL RELAXATION
FLUOROPHORES
Аннотация:
A new approach is proposed for interpreting the polarized
fluorescence
spectra of an impure liquid crystal in which the orientational order of excited impurity molecules has undergone relaxation. This approach has also been realized experimentally. The new experimental data demonstrate a new relaxation process with a time scale on the order of 10(-11)-10(-9) s.
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12.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Vtyurin A. N., Krylov A. S., Voronov V. N., Krylova S. N.
Заглавие
: Raman scattering and phase transitions in fluorides with elpasolite structure
Коллективы
: Joint Russia/CIS/Baltic/Japan Symposium on Ferroelectricity, International Workshop on Relaxor Ferroelectrics
Место публикации
: Ferroelectrics: Proceedings of the Joint International Symposium. - 2017. - Vol. 512, Is. 1. - P.58-64. - ISSN 00150193 (ISSN),
DOI
10.1080/00150193.2017.1349863
Примечания
: Cited References: 22
Ключевые слова
(''Своб.индексиров.''): ferroelectric materials--ferroelectricity--elpasolite--first-order phase transitions--
fluorescence
process--raman lines--raman scattering spectra--temperature phase--temperature range--raman scattering
Аннотация:
Raman scattering spectra of Rb2KHoF6 and Rb2KDyF6 crystals have been studied in temperature range from 20 K to 399 K and from 7 K to 500 K respectively. Raman spectra of Rb2KHoF6 crystal are distorted due to the
fluorescence
process. Parameters of Raman lines have been quantitatively analyzed. The investigation points to the considerable role of CX6 groups in the temperature phase transition in Rb2KHoF6 and Rb2KDyF6 crystals. The anomalies of spectra changes with temperature testify the first order phase transitions in these crystals. © 2017 Taylor & Francis Group, LLC.
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13.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Gerasimova M. A., Tomilin F. N., Malyar E. Y., Varganov S. A., Fedorov D. G., Ovchinnikov S. G., Slyusareva E. A.
Заглавие
:
Fluorescence
and photoinduced proton transfer in the protolytic forms of fluorescein: Experimental and computational study
Место публикации
: Dyes Pigm. - 2020. - Vol. 173. - Ст.107851. - ISSN 01437208 (ISSN),
DOI
10.1016/j.dyepig.2019.107851
Примечания
: 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 ).
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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14.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Dong R., Yao Y., Li D., Zhang H., Li W., Molokeev M. S., Liu Y., Lei B.
Заглавие
: Ratio fluorescent hybrid probe for visualized
fluorescence
detection of H2O2 in vitro and in vivo
Место публикации
: Sens. Actuators B: Chem. - 2020. - Vol. 321. - Ст.128643. - ISSN 09254005 (ISSN),
DOI
10.1016/j.snb.2020.128643
Примечания
: Cited References: 65. - The present work was supported by the National Natural Science Foundations of China (Grant No. 21671070 ), the project supported by the GDUPS (2018) for Prof. Bingfu LEI, the Project for Construction of High-level University in Guangdong Province of China, the Guangzhou Science & Technology Project , China (No. 201707010033 ), the Special Funds for the Cultivation of Guangdong College Students’ Scientific and Technological Innovation (No. 201910564035 ), and the National Undergraduate Innovation and Entrepreneurship Training Program granted for Riyue Dong
Аннотация:
A silicon oxide quantum dots (Si-O QDs) and Ag nanoclusters hybrid nanosensing probe with dual-emission and small nanocrystals that acts as an “off-on” ratio fluorescent probe for hydrogen peroxide (H2O2) detection was developed. The probe was used to measure the H2O2 concentration generated by mitochondria in vitro via recording the I455/I680
fluorescence
ratio. Furthermore, this hybrid probe was applied to monitor the wound-induced H2O2 in lettuce leaf, and realized the visualized
fluorescence
qualitative detection H2O2 in vivo via laser scanning confocal microscope. The working mechanism of the probe is also investigated. Inner filter effect (IFE) estimation, Fourier transform infrared (FTIR) spectra and high-resolution transmission electron microscopy (HRTEM) images were applied to study the quenching mechanism and recovering reason of Si-O QDs
fluorescence
. The results show that the blue
fluorescence
of Si-O QDs can be quenched by Ag NCs via the IFE and fluorescent resonance energy transfer (FRET) effect. After adding H2O2, the surface groups of Ag NCs was changed and the IFE and FRET effects between the Si-O QDs and Ag NCs are disabled, thus the quenched Si-O QDs luminescence can be regularly recovered.
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15.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Zhang, Guangqing, Molokeev M. S., Ma, Qianchao, Yang, Xuening, Han, Shuiquan, Chen, Q.i., Zhong, Binnian, Ma, Bin
Заглавие
: Structural analysis and optical temperature sensing performance of Eu3+-doped Ba3In(PO4)3
Место публикации
: CrystEngComm. - 2020. - Vol. 22, Is. 35. - P.5809-5817. - ISSN 1466-8033,
DOI
10.1039/d0ce00997k
Примечания
: Cited References: 52. - This work was supported by the National Natural Science Foundation of China (Grant No. 51802172) and the Qinghai Provincial Natural Science Foundation for Young Scholars (No. 2018-ZJ-957Q)
Предметные рубрики:
FLUORESCENCE
INTENSITY RATIO
UP-CONVERSION EMISSIONS
RARE-EARTH IONS
Аннотация:
Eu3+-Doped Ba3In(PO4)3 was synthesized through a high-temperature solid-phase method. According to the structure refinement based on X-ray diffraction and density functional theory, the crystal and energy band structures of Ba3In(1−x)(PO4)3:xEu3+ were studied and analyzed in detail. The effect of Eu3+ doping concentrations on emission was studied at an excitation wavelength of 393 nm. For the material Ba3In(1−x)(PO4)3:xEu3+(x = 0.01–0.30), the optimal doping level is confirmed to be 0.18. Due to the thermal quenching differences of Eu3+ at the 5D0 and 5D1 energy levels, and based on the temperature-variable
fluorescence
intensity ratio between emission peaks, the optical temperature measurement performance of this material in the temperature range from 298.15 K to 623.15 K was characterized, and the maximum absolute and relative sensor sensitivities (Sa and Sr) were determined to be 0.1002 K−1 and 4.058%, respectively. With temperature as the only variable, the color of the phosphor changes from red to yellow light with rising temperature. Besides, Sa and Sr values of this phosphor are comparable to other sensing materials. The results indicate that Eu3+-doped Ba3In(PO4)3 phosphors have great potential to be applied in optical temperature sensing.
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16.
Вид документа
: Статья из сборника (выпуск монографической серии)
Шифр издания
:
Автор(ы)
: Bukhanov E. R., Gurevich Y. L., Shabanova K. A.
Заглавие
: A study of wheat wax optical properties
Коллективы
: Photonics and Electromagnetics Research Symposium - Fall
Место публикации
: Photonics and Electromagnetics Research Symposium - Fall (2019 ; Dec 17-20 ; Xiamen, China). Photonics & Electromagnetics Research Symposium - Fall (PIERS - Fall): IEEE, 2019. - P.2890-2897. - (Progress in Electromagnetics Research Symposium). - ,
DOI
10.1109/PIERS-Fall48861.2019.9021781
Примечания
: Cited References: 36
Предметные рубрики:
DIMENSIONAL PHOTONIC CRYSTALS
BLUE-GREEN
FLUORESCENCE
Аннотация:
Epicuticular waxes are a multifunctional interface between a plant and the environment. In this paper wheat leaves wax has been studied. Wax isolation was carried out using the method of gradual freezing in water followed by slow thawing. The morphology of the samples obtained was observed with a Hitachi SU3500 electron microscope. The structure period is determined by the nanotubes diameter which equals 150-200 nm. Random orientation of their long axes in the layer allows using a one-dimensional model to calculate the transmission spectrum of a photonic crystal with the help of the transfer matrix method. While making the calculations a defect that may be caused by possible interlayer heterogeneity also must be taken into account. Numerical modeling made it possible to identify the stop zone and the defective mode. Intense
fluorescence
appears in the optical area of the wax layer under ultraviolet radiation, thus increasing the efficiency of photosynthesis.
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17.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Буханов, Евгений Романович, Шабанов, Александр Васильевич, Крахалев, Михаил Николаевич, Волочаев, Михаил Николаевич, Гуревич, Юрий Леонидович
Заглавие
: Влияние строения на оптические свойства эпикулярного воска голубой ели (Picea pungens)
Место публикации
: Ученые зап. физ. фак-та МГУ. - 2019. - № 5. - Ст.1950502. - ISSN 2307-9665 (eISSN)
Примечания
: Библиогр.: 36
Аннотация:
Выполнено исследование морфологических и оптических характеристик с эпикулярного воскового слоя голубой ели (Picea pungens). Методом сканирующей электронной микроскопии выявлены структурные единицы – трубочки диаметром 150-200нм и длиной 3-5 мкм. Обнаружен эффект иризации от доменов воскового слоя. В отраженном свете домены имею голубую окраску, при наблюдении в проходящем свете приобретают розоватый оттенок. Эти оптические характеристики являются основными признаками фотоннокристаллической структурой. Проведено численное моделирование спектра пропускания с выявленными структурными оптическими параметрами с использованием метода трансфер матриц. Спектр максимума флюоресценции совпадает с дефектной модой рассчитанного спектра пропускания.The study of morphological and optical characteristics of the epicular wax layer of blue spruce (Picea pungens). The method of scanning electron microscopy revealed structural units - tubes with a diameter of 150-200 nm and a length of 3-5 microns. An iridescence effect from the wax layer domains has been detected. In the reflected light, the domains have a blue color, when observed in transmitted light acquire a pinkish tint. These optical characteristics are the main features of the photonic crystal structure. A numerical simulation of the transmission spectrum with the identified structural optical parameters was carried out using the transfer matrix method. The spectrum of the maximum fluorescence coincides with the defect mode of the calculated transmission spectrum.
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РИНЦ
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18.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Rogova A. V., Tomilin F. N., Gerasimova M. A., Slyusareva E. A.
Заглавие
: Modeling of Electronic Spectra of Ionic Forms of Eosin and Erythrosin
Место публикации
: Russ. Phys. J. - 2020. - Vol. 63, Is. 8. - P.1417-1423. - ISSN 10648887 (ISSN),
DOI
10.1007/s11182-020-02186-1
Примечания
: Cited References: 17
Аннотация:
Multistage dissociation of fluoroscein dyes, widely used in biological labeling, yields a variety of ionic and tautomeric forms in a wide range of pH values. In contrast to well-studied absorption spectra, the emission spectra are not quite readily interpreted due to their strong overlapping and proton transfer in electronically excited states. The least studied are the fluorescent properties of eosin and erythrosin dyes containing heavy atoms (Br, I), in which the characteristics of the dianionic form only are reliably determined. In the framework of the density functional theory using the B3LYP-functional including nonequilibrium solvation, the geometries of the series of ionic forms of eosin and erythrosin in the ground and excited states are found, and the electronic spectra are calculated. Based on the identified linear regression of the calculated and experimental data for the earlier resolved electronic spectra, for the first time, the emission spectrum maxima of the monoanionic, neutral quinoid, and cationic forms of the dyes are determined. The spectral peculiarities (Stokes shifts) are discussed in terms of variation of the molecule and ion geometries in the ground and excited states.
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19.
Вид документа
: Статья из сборника (выпуск продолж. издания)
Шифр издания
:
Автор(ы)
: Bukhanov E. R., Gurevich Y., Krakhalev M. N., Shabanov D. A.
Заглавие
: Modeling optical properties of plant epicuticular wax
Коллективы
: IEEE International Conference on Information Technology and Nanotechnology
Место публикации
: Proceedings of ITNT 2020 - 6th IEEE International Conference on Information Technology and Nanotechnology: Institute of Electrical and Electronics Engineers Inc., 2020. - Ст.9253272. -
DOI
10.1109/ITNT49337.2020.9253272
Примечания
: Cited References: 39
Аннотация:
Wax is found on the leaves almost of all plants. Its physicochemical and protective properties are widely discussed in the scientific literature. In the presented work, the influence of the structure of wax on the optical properties in wheat leaves and needles of blue spruce has been revealed for the first time. Long-period ordering was established. The structural elements are nanotubes up to several microns in length and about 150 nm in diameter. The paper presents the influence of a long-period structure on the optical properties and local characteristics of light waves, including the transmission spectrum, the density of photon states, as well as
fluorescence
spectra and polarization microscopy. Using modern mathematical tools, the main spectral and optical characteristics were calculated using the example of the wax cover of blue spruce and glaucas wheat. Based on calculations that establish the relationship between the structural, spectral and optical properties, the influence of wax structures on the process of photosynthesis was revealed.
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20.
Вид документа
: Статья из журнала
Шифр издания
:
Автор(ы)
: Lin C. -R., Ivanova O. S., Petrov D. A., Sokolov A. Е., Chen Y. -Z., Gerasimova M. A., Zharkov S. M., Tseng Y. -T., Shestakov N. P., Edelman I. S.
Заглавие
: Amino-functionalized Fe3O4@SiO2 core-shell magnetic nanoparticles for dye adsorption
Место публикации
: Nanomaterials. - 2021. - Vol. 11, Is. 9. - Ст.2371. - ISSN 20794991 (ISSN),
DOI
10.3390/nano11092371
Примечания
: Cited References: 35. - The authors are thankful for the financial support the Russian Foundation for Basic Research, Grant № 19-52-52002, Ministry of Science and Technology of Taiwan, Grants MOST № 108-2923-M-153-001-MY3 and № 109-2112-M-153-003-, the Russian Foundation for Basic Research with Government of Krasnoyarsk Territory, Krasnoyarsk Regional Fund of Science, the research project number 19-42-240005: “Features of the electronic structure, magnetic properties and optical excitations in nanocrystals of the multifunctional magnetic chalcogenides Fe3S4 and FeSe”. We thank also the SFU Joint Scientific Center 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
Аннотация:
Fe3O4@SiO2 core-shell nanoparticles (NPs) were synthesized with the co-precipitation method and functionalized with NH2 amino-groups. The nanoparticles were characterized by X-ray, FT-IR spectroscopy, transmission electron microscopy, selected area electron diffraction, and vibrating sample magnetometry. The magnetic core of all the nanoparticles was shown to be nanocrystalline with the crystal parameters corresponding only to the Fe3O4 phase covered with a homogeneous amorphous silica (SiO2) shell of about 6 nm in thickness. The FT-IR spectra confirmed the appearance of chemical bonds at amino functionalization. The magnetic measurements revealed unusually high saturation magnetization of the initial Fe3O4 nanoparticles, which was presumably associated with the deviations in the Fe ion distribution between the tetrahedral and octahedral positions in the nanocrystals as compared to the bulk stoichiometric magnetite. The fluorescent spectrum of eosin Y-doped NPs dispersed in water solution was obtained and a red shift and line broadening (in comparison with the dye molecules being free in water) were revealed and explained. Most attention was paid to the adsorption properties of the nanoparticles with respect to three dyes: methylene blue, Congo red, and eosin Y. The kinetic data showed that the adsorption processes were associated with the pseudo-second order mechanism for all three dyes. The equilibrium data were more compatible with the Langmuir isotherm and the maximum adsorption capacity was reached for Congo red.
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