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Каталог книг и продолжающихся изданий
Сводный каталог иностранных периодических изданий, имеющихся в библиотеках УрО РАН
Сводный каталог отечественных периодических изданий, имеющихся в библиотеках УрО РАН
Каталог диссертаций и авторефератов диссертаций УрО РАН
Каталог препринтов УрО РАН (1975 г. - )
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Демидовские премии
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История Урала
Личная библиотека С. В. Вонсовского
Книжная коллекция Шубиных
Труды Института высокотемпературной электрохимии УрО РАН
Труды Института истории и археологии УрО РАН
Труды сотрудников Института горного дела УрО РАН
Труды сотрудников Института органического синтеза УрО РАН
Труды сотрудников Института теплофизики УрО РАН
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Труды сотрудников ЦНБ УрО РАН
Публикации Черешнева В.А.
Публикации Чарушина В.Н.
Каталог библиотеки ИЭРиЖ УрО РАН
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1.
Инвентарный номер: нет.
   

   
    2,2 '-Bipyridinyl carboranes as B,N,N-ligands in cyclometallated complexes of platinum(II) [] / A. M. Prokhorov, P. A. Slepukhin, V. L. Rusinov, V. N. Kalinin, D. N. Kozhevnikov // Chemical Communications. - 2011. - Vol. 47, № 27. - С. 7713-7715
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
O-CARBORANE -- METALLACARBORANES -- PHOTOLUMINESCENT
Аннотация: Novel B,N,N-cyclometallated Pt(II) complexes of 2,2'-bipyridin-6-yl carboranes exhibit absorption and emission similar to relative Pt(II) complexes of aromatic C,N,N-ligands: the same transitions but lower intensities. DFT calculations suggest the former emits from the (3)MLCT state while for the latter the mixed (3)ICT-MLCT transitions should be considered

\\\\expert2\\NBO\\Chemical Communications\\2011,v.47. p.7713.pdf
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2.
Инвентарный номер: нет.
   
   A 67

   
    Application of chitosan and its N-heterocyclic derivatives forpreconcentration of noble metal ions and their determination usingatomic absorption spectrometry / Yu. A. Azarova, A. V. Pestov, A. Yu. Ustinov, S. YU. Bratskaya // Carbohydrate Polymers. - 2015. - Vol. 134. - С. 680-686
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN -- N-HETEROCYCLIC DERIVATIVES -- SPECTROMETRY

\\\\expert2\\NBO\\Carbohydrate Polymers\\2015, v. 134, p. 680.pdf
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3.
Инвентарный номер: нет.
   

   
    Conjugates of 8-[2,2’-bipyridinyl]coumarins as potential chemosensors for Al3+, Cu2+, Cd2+, Zn2+ ions: synthesis and photophysical properties / A. D. Sharapov, R. F. Fatykhov, I. A. Khalymbadzha [et al.] // Chimica Techno Acta. - 2023. - Vol. 10, № 4. - P202310417
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHEMOSENSORS -- COUMARINS -- 2,2’-BIPYRIDINES
Аннотация: In this work, we report the synthesis of novel coumarin-bipyridine conjugates using a sequence of C-C coupling reaction between 5,7-dimethoxycoumarins and 3-pyridyl-6-aryl-1,2,4-triazines followed by the Boger reaction with norbornandiene to obtain 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins. Photophysical properties were investigated for the obtained series of 8-[2,2'-bipyridyl]-5,7-dimethoxycoumarins: absorption and emission wavelength maxima are in the region of 212-296 and 401-410 nm, respectively; Stokes shifts are up to 116 nm, and fluorescence quantum yields are up to 15.0%. It was found that titrating the conjugates with Al3+, Zn2+, and Cd2+ ions results in an increase in the intensity of the emission maxima of the complexes, while the opposite effect was observed in the case of titration with Cu2+ ions. These findings suggest that the studied compounds may be considered as promising chemosensing materials. Finally, a positive solvatochromism of 8-[2,2'-bipyridyl]coumarins and their metal complexes was established. The experimental data are supported by mathematical calculations according to the Lippert-Matagaequation and Kosower diagram.

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4.
Инвентарный номер: нет.
   

   
    Coumarin-pyridine push-pull fluorophores: synthesis and photophysical studies / R. F. Fatykhov, A. D. Sharapov, E. S. Starnovskaya [et al.] // Spectrochimica acta part A: molecular and biomolecular spectroscopy. - 2022. - Vol. 267. - Ст. 120499
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A series of coumarin-pyridine-based push-pull fluorophores were prepared starting from 1,2,4-triazines by using direct C-H functionalization (SNH-reaction)–Diels-Alder–retro Diels-Alder domino reaction sequence. This efficient synthetic strategy allowed to obtain a series of 19 coumarin-pyridine fluorophores. Their photophysical properties were studied. While pyridine-substituted derivatives of 4-alkylcoumarins may be considered as alternative to coumarin dyes characterized by emission maxima mainly in a visible region with wavelengths of 402–415 nm, absorption in the UV range at 210–307 nm, and good photoluminescence quantum yields of 6–19%, all the derivatives of 4-phenylcoumarin did not exhibit any noticeable fluorescence. More detailed photophysical studies were carried out for two the most representative derivatives of 4-alkyl-coumarin-pyridines to demonstrate their positive solvatochromism, and the collected data were analyzed by using Lippert-Mataga equation, as well as Kosower and Dimroth/Reichardt scales. The obtained results demonstrate that the combining two chromophore systems, such as 2,5-diarylpyridine and coumarin ones, is promising in terms of improving the photophysical properties of the new coumarin-pyridine hybrid compounds.

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5.
Инвентарный номер: нет.
   
   D 64

   
    Dithienoquinazolines – A Convenient Synthesis by the Oxidative Photocyclization of 4,5-Dithienyl-Substituted Pyrimidines and Their Photophysical Properties [Electronic resource] / E. V. Verbitskiy, P. A. Slepukhin, M. S. Valova, E. M. Cherprakova, A. V. Schepochkin, G. L. Rusinov, V. N. Charushin // European Journal of Organic Chemistry. - 2014. - № 36. - С. 8133-8141
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
DITHIENOQUINAZOLINES -- PYRIMIDINES -- PHOTOPHYSICAl PROPERTIES
Аннотация: A convenient route to a new class of thienoacene systems bearing a fused pyrimidine ring is presented along with their optoelectronic properties. The photophysical and electrochemical properties of these newly developed thieno-aza-acenes have been investigated by UV/Vis absorption and photoluminescence spectrophotometry and cyclic voltammetry, and some crystal structures have also been determined.

\\\\expert2\\nbo\\European Journal of Organic Chemistry\\2014, № 36. p.8133-8141.pdf
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6.
Инвентарный номер: нет.
   
   F 97

   
    Fundamental absorption edge of NiO nanocrystals [Electronic resource] / V. I. Sokolov, A. V. Druzhinin, D. G. Kim, N. B. Gruzdev, A. Ye. Yermakov, M. A. Uimin, I. V. Byzov, N. N. Shchegoleva, V. B. Vykhodets, T. E. Kurennykh // Physica B: Condensed Matter . - 2013. - Vol. 430. - С. 1-5. - Bibliogr. : p. 5 (29 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
TRANSITION METAL OXIDE -- OPTICAL PROPERTIES -- CHARGE TRANSFER TRANSITIONS
Аннотация: NiO nanocrystals with the average size of 5, 10 and 25 nm were synthesized by gas-condensation method. The well-defined increase of the optical density D near the fundamental absorption edge of NiO nanocrystals in the range of 3.5–4.0 eV observed after the annealing in air is caused by the oxygen content growth. It is the direct experimental evidence of the fact that p—d charge transfer transitions form the fundamental absorption edge

\\\\expert2\\NBO\\Physica B\\2013, v.430, p. 1-5.pdf
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7.
Инвентарный номер: нет.
   
   N 10

   
    N-(2-(2-pyridyl)ethyl)chitosan: Synthesis, characterization and sorption properties / S. YU. Bratskaya, Yu. A. Azarova, E. G. Matochkina, M. I. Kodess, Yu. G. Yatluk, A. V. Pestov // Carbohydrate Polymers. - 2012. - Vol. 87, № 1. - С. 869-875
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CHITOSAN N-HETEROCYCLIC DERIVATIVES -- SELECTIVE ADSORPTION -- PYRIDINE DERIVATIVES
Аннотация: The method of producing N-2-(2-pyridyl)ethylchitosan (PE-chitosan) with substitution degrees (DS) up to 1.2 has been developed using the "synthesis in gel" approach for direct addition reaction between 2-vynilpyridine and chitosan. Investigation of sorption properties has revealed significantly higher affinity of pyridylethyl fragments to Pt(IV)) and Pd(II) ions compared to the unsubstituted amino groups of chitosan. The maximum sorption capacities of PE-chitosan in 0.1 M HCl solution were estimated as 5.56 mmol/g for Au(III), 3.67 mmol/g for Pd(II), and 2.75 mmol/g for Pt(IV). Sorption capacities of PE-chitosan for transition metal ions at pH 4-8 were 1.5-2.6 higher than those of chitosan with the highest values attained for Cu(II) and Ag(I) ions - 1.50 mmol/g and 1.53 mmol/g, respectively. The PE-chitosan application for preconcentration of Au(III) with subsequent elution with HCl/thiourea mixtures was proved to be efficient for atomic absorption spectroscopy analysis of multi-component solutions with low gold content

\\\\Expert2\\nbo\\Carbohydrate Polymers\\2012, v. 87, p.869.pdf
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8.
Инвентарный номер: нет.
   
   N 10

   
    N-(2-(2-pyridyl)ethyl)chitosan: synthesis, characterization and sorption properties [Text] / S. YU. Bratskaya, Yu. A. Azarova, E. G. Matochkina, M. I. Kodess, Yu. G. Yatluk, A. V. Pestov // Carbohydrate Polymers. - 2011. - In Press, Accepted Manuscript, Availabe online 31 Augist 2011
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The method of producing N-2-(2-pyridyl)ethylchitosan (PE-chitosan) with substitution degrees (DS) up to 1.2 has been developed using the “synthesis in gel” approach for direct addition reaction between 2-vynilpyridine and chitosan. Investigation of sorption properties has revealed significantly higher affinity of pyridylethyl fragments to Pt(IV)) and Pd(II) ions compared to the unsubstituted amino groups of chitosan. The maximum sorption capacities of PE-chitosan in 0.1 M HCl solution were estimated as 5.56 mmol/g for Au(III), 3.67 mmol/g for Pd(II), and 2.75 mmol/g for Pt(IV). Sorption capacities of PE-chitosan for transition metal ions at pH 4-8 were 1.5-2.6 higher than those of chitosan with the highest values attained for Cu(II) and Ag(I) ions–1.50 mmol/g and 1.53 mmol/g, respectively. The PE-chitosan application for preconcentration of Au(III) with subsequent elution with HCl/thiourea mixtures was proved to be efficient for atomic absorption spectroscopy analysis of multi-component solutions with low gold content

\\\\Expert2\\nbo\\Carbohydrate Polymers\\2011, Article inPress, 31 August.pdf
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9.
Инвентарный номер: нет.
   

   
    New 2,5-bis(2-ethylhexyl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione-2,2’-bipyridine-based co-polymer, synthesis, photophysical properties and response to metal cations / A. P. Krinochkin, M. I. Savchuk, E. S. Starnovskaya [et al.] // Chimica Techno Acta. - 2021. - Vol. 8, № 4. - Ст. 20218417
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SONOGASHIRA COUPLING -- POLYMER -- MONOAZATRIPHENYLENE -- 3,6-DI(THIOPHEN-2- YL)PYRROLO[3,4-C]PYRROLE- 1,4(2H,5H)-DIONE
Аннотация: A new co-polymer based on fragments of 2-(2-pyridyl)monoazatriphenylene and 2,5-bis (2-ethylhexyl)-3,6-di(thiophen-2-yl)pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione was prepared by using the Sonogashira reaction. The photophysical properties of the polymer were studied. The presence of a strong bathochromic shift of the absorption and emission maxima in comparison with the previously described monomer units is shown. The polymer exhibits an intense “turn-off” response toward Cu2+ cations.

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10.
Инвентарный номер: нет.
   
   P 58

   
    Phosphorescence vs Fluorescence in Cyclometalated Platinum(II) and Iridium(III) Complexes of (Oligo)thienylpyridines / D. N. Kozhevnikov, V. N. Kozhevnikov, M. Z. Shafikov, A. M. Prokhorov, D. W. Bruce, J. A. Gareth Williams // Inorganic Chemistry . - 2011. - Vol. 50, № 8. - С. 3804-3815
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
OLIGOTHIENYLPYRIDINES -- LIGANDS -- LUMINESCENCE PROPERTIES
Аннотация: Two newly prepared oligothienylpyridines, 5-(2-pyridyl)-5?-dodecyl-2,2?-bithiophene, HL2, and 5-(2-pyridyl)-5??-dodecyl-2,2?:5?,2??-ter-thiophene, HL3, bind to platinum(II) and iridium(III) as NC-coordinating ligands, cyclometallating at position C4 in the thiophene ring adjacent to the pyridine, leaving a chain of either one or two pendent thiophenes. The synthesis of complexes of the form [PtLn(acac)] and [Ir(Ln)2(acac)] (n = 2 or 3) is described. The absorption and luminescence properties of these four new complexes are compared with the behavior of the known complexes [PtL1(acac)] and [Ir(L1)2(acac)] {HL1 = 2-(2-thienyl)pyridine}, and the profound differences in behavior are interpreted with the aid of time-dependent density functional theory (TD-DFT) calculations. Whereas [PtL1(acac)] displays solely intense phosphorescence from a triplet state of mixed ??*/MLCT character, the phosphorescence of [PtL2(acac)] and [PtL3(acac)] is weak, strongly red shifted, and accompanied by higher-energy fluorescence. TD-DFT reveals that this difference is probably due to the metal character in the lowest-energy excited states being strongly attenuated upon introduction of the additional thienyl rings, such that the spin?orbit coupling effect of the metal in promoting intersystem crossing is reduced. A similar pattern of behavior is observed for the iridium complexes, except that the changeover to dual emission is delayed to the terthiophene complex [Ir(L3)2(acac)], reflecting the higher degree of metal character in the frontier orbitals of the iridium complexes than their platinum counterparts.??

\\\\Expert2\\nbo\\Inorganic Chemistry\\2011, v.50, p.3804.pdf
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11.
Инвентарный номер: нет.
   
   P 58

   
    Photophysics, photochemistry and bioimaging application of 8-azapurine derivatives / A. K. Eltyshev, I. A. Agafonova, A. S. Minin [et al.] // Organic & biomolecular chemistry. - 2021. - Vol. 19, № 45. - P9880-9896
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: New 2-aryl-1,2,3-triazolopyrimidines were designed, synthesized, and characterized. Their optical properties were thoroughly studied in the solid phase, in solution and in a biological environment. Density Functional Theory (DFT) based calculations were performed, including the molecular geometry optimization for both the ground state and the first singlet excited state, the prediction of the UV-Vis absorption and fluorescence spectra, the determination of the molecular electrostatic properties and the solvent effect on the optical properties. The emission intensity was revealed to increase in time upon irradiation. Mass spectrometric research, quantum mechanical calculations, and analysis of literature data suggested a possible photo-transformation pathway through the homolytic cleavage of one of the C–Cl bonds upon irradiation with UV light. The structure of the active intermediate was identified by the series of mass spectrometry experiments and via synthesis of putative transformation products. The kinetic parameters measured in different solvents allowed estimating the rate of these photo-transformations. Biological experiments demonstrated that 2-aryl-1,2,3-triazolopyrimidines penetrate cells and selectively accumulate in the cell membrane and the Golgi complex and endoplasmic reticulum. Their unique properties pave the way for new possible applications of fluorescent 8-azapurines in biology and medicine.

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12.
Инвентарный номер: нет.
   
   P 93

   
    Protolytic Equilibria of Some N,N-Bis(2-carboxyethyl)aminoazobenzenesulfonic Acids in Aqueous Solution [Electronic resource] / Yu. A. Skorik, L. K. Neudachina, A. V. Osintsev, Yu. G. Yatluk, A. A. Vshivkov, E. V. Osintseva // Russian Journal of Organic Chemistry (Translation of Zhurnal Organicheskoi Khimii). - 2002. - Vol. 38, № 3. - P385-389
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: 4-[4-Bis(2-carboxyethyl)aminophenylazo]benzenesulfonic acid and 4-[2-bis(2-carboxyethyl)amino-4,5-dimethylphenylazo]benzenesulfonic acid were synthesized for the first time by azo coupling of diazosulfanilic acid with N,N-bis(2-carboxyethyl)aniline and N,N-bis(2-carboxyethyl)-3,4-xylidine, respectively. The acid ionization constants of the products were determined, their electron absorption spectra were measured, and schemes of acid-base equilibria in aqueous solution were proposed

\\\\Expert2\\nbo\\Russian Journal of Organic Chemistry\\2002, 38 (3), 385.pdf
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13.
Инвентарный номер: нет.
   
   O-84

    Osintseva, E. V.
    Protolytic properties and complexation with copper(II) ions of some azo derivatives of beta-arylaminopropionic acids [Electronic resource] / E. V. Osintseva, L. K. Neudachina, Yu. G. Yatluk // Russian Journal of Inorganic Chemistry (Zhurnal Neorganicheskoi Khimii). - 2010. - Vol. 55, № 10. - P1644-1650
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The azo coupling reaction of N-(2-carboxyethyl)anthranilic acid and N,N,N,N-tetrabis(2-carboxyethyl)-1,3-phenylenediamine with diazosulfanilic acid yielded the complexones sodium 4-N-(2-carboxyethyl)amino-5-carboxyazobenzene-4?-sulfonate (I) and 2,4-N,N,N,N-tetrabis(2-carboxyethyl)diaminoazobenzene-4?-sulfonic acid (II), respectively. The acidity constants of I and II (20°C = 0.1M KCl) were determined to be as follows: for I, pK 00 = 1.29 ± 0.13, pK 0 = 2.92 ± 0.07, pK 1 = 3.92 ± 0.05, pK 2 = 5.16 ± 0.03; for II, pK 00 = 2.35 ± 0.06, pK 0 = 2.81 ± 0.09, pK 1 = 3.21 ± 0.11, pK 2 = 3.81 ± 0.09, pK 3 = 4.34 ± 0.04, pK 4 = 5.03 ± 0.06, pK 5 = 6.67 ± 0.07. The electronic absorption spectra of I and II were measured, and acid-base equilibrium scheme for I and II in aqueous solutions were suggested. The complexation constants of I and II with copper(II) ions were determined to be logK CuQI= 5.47 ± 0.06 and logK CuQII= 5.72 ± 0.13 (20°C = 0.1 M KCl). ??

\\\\Expert2\\nbo\\Russian Journal of Inorganic Chemistry\\2010, v. 55, N 10, с.1644.pdf
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14.
Инвентарный номер: нет.
   
   S 89

   
    Structure and absorption spectra of substituted 2-hydroxy-2-trifluoromethylchroman-4-ones / L. A. Khamidullina, I. S. Puzyrev, A. V. Pestov, V. S. Moshkin, Yu. G. Yatluk // Journal of Applied Spectroscopy. - 2012. - Vol.79, №4. - С. 509-514
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ABSORPTION SPECTRA -- EXTINCTION COEFFICIENT -- MEDIUM ACIDITY
Аннотация: UV absorption spectra of substituted 2-hydroxy-2-trifluoromethylchroman-4-ones (chromanones) in aqueous ethyleneglycol were studied. Replacement of hydrogen in the aromatic ring of the chromanones by CH3 or CF3 groups was shown to cause the molar extinction coefficients of the K, B, and C=O bands to shift from 16,160 to 27,980 and 30,250 dm(3)/mol center dot cm; from 12,750 to 17,920 and 16,130 dm(3)/mol center dot cm; and from 3850 to 3630 and 2760 dm(3)/mol center dot cm, respectively. Increasing the solution pH from 1 to 10.5 affected weakly the aromatic ring bands yet impacted greatly the chromanone carbonyl bands, causing their lambda(max) to shift from 311-326 nm to 342-346 nm and their extinction coefficients to increase from 2760-3850 dm(3)/mol center dot cm to 9940-10,160 dm(3)/mol center dot cm. A further rise in the pH resulted in hypochromia of the carbonyl band due to the destruction of the chromanones. The results were confirmed by NMR spectroscopy and GC methods

\\\\Expert2\\nbo\\Journal of Applied Spectroscopy\\2012, v. 90, p.1176.pdf
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15.
Инвентарный номер: нет.
   
   S 89

   
    Structure and photoluminescent properties of 2-methyl-6,7-difluoro-8-hydroxyquinoline [Electronic resource] / G. N. Lipunova, E. V. Nosova, J. O. Subbotina, M. S. Valova, V. N. Charushin // Russian Journal of General Chemistry. - 2015. - Vol. 85, № 7. - С. 1629-1634. - Bibliogr. : p. 1634 (19 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2-METHYL-6,7-DIFLUORO-8-HYDROXYQUINOLINE -- ABSORPTION SPECTRUM -- EXCITATION SPECTRUM
Аннотация: The effect of fluorine atoms in the benzene ring on the photophysical properties of 2-methyl-6,7-difluoro-8-hydroxyquinoline is studied.

\\\\expert2\\nbo\\Russian Journal of General Chemistry\\2015, V. 85, N 7, p. 1629-1634.pdf
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16.
Инвентарный номер: нет.
   
   S 90

   
    Studying the electronic structure of Cr (x) Ti(1-x) Se(2) by X-ray resonance and absorption spectroscopy [Text] / A. S. Shkvarin, Yu. M. Yarmoshenko, N. A. Skorikov, A. I. Merentsov, A. N. Titov, P. A. Slepukhin, D. E. Marchenko, M. Sperling // Journal of experimental and theoretical physics. - 2011. - Vol. 112, № 1. - P87-93. - Bibliogr. : p. 93 (19 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Cr (x) Ti(1 - x) Se(2) (x = 0-0.83) solid solutions have been synthesized. Single crystals have been grown in the range of concentrations x = 0-0.83. Structural studies of samples have revealed that chromium atoms substitute titanium in the TiSe(2) matrix. The X-ray photoelectron spectra of the core levels, the resonance spectra of the valence bands in 1T-Cr (x) Ti(1 - x) Se(2), and the X-ray absorption spectra of titanium and chromium are studied. The titanium and chromium atoms are shown to have oxidation numbers of +4 and +3, respectively, in an identical octahedral environment. The local density of chromium states has been calculated. The results of the calculation agree well with the experimental data and indicate that the electronic 3d states of chromium substituting titanium in the matrix are spin-polarized and the density of chromium states is halfmetal magnet in behavior

\\\\Expert2\\nbo\\Journal of Experimental and Theoretical Physics\\2011, v.112, N 1, P. 87.pdf
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17.
Инвентарный номер: нет.
   

   
    Synthesis and photophysical studies of novel v-shaped 2,3-bis{5-aryl-2-thienyl}(dibenzo[f,h])quinoxalines / T. N. Moshkina, E. V. Nosova, A. E. Kopotilova [et al.] // Asian journal of organic chemistry. - 2020. - Vol. 9, № 4. - P673-681
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
CROSS-COUPLING -- DIBENZO[F,H]QUINOXALINE -- DONOR-ACCEPTOR-DONOR CHROMOPHORES -- FLUORESCENCE -- SENSORS
Аннотация: A series of novel V-shaped luminophores containing electron-withdrawing dibenzo[f,h]quinoxaline core and arylthienyl donor fragments at positions 2 and 3 has been synthesized. The absorption spectra (UV/vis) were recorded in several solvents, whereas emission spectra were recorded in solutions and powders. The solvatochromism as well as halochromism of obtained compounds was also explored. Electronic-structure calculations using quantum-chemistry methods were performed to further analyse experimental results. All characteristics were compared with that of 2,3-bis(arylthienyl)quinoxaline counterparts. The halochromic effect studies showed that upon gradual addition of trifluoroacetic acid (TFA) to the toluene solution of diethylaminophenyl-substituted dibenzo[f,h]quinoxaline chromophore, absorption and emission changed. Observed band shifts were more distinct in the case of mentioned quinoxaline than for other derivatives. All of the (dibenzo[f,h])quinoxaline chromophores exhibited good sensitivity toward nitro-containing explosives with high Stern-Volmer constants up to 57800 M−1, these results are remarkable for such heterocyclic systems.

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18.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and properties of epoxy-anhydride polymers modified with polyfluorolakyl-substituted oxiranes in the course of curing [Electronic resource] / M. S. Fedoseev, L. F. Derzhavinskaya, V. I. Karmanov, D. N. Bazhin, A. Ya. Zapevalov, T. I. Gorbunova, V. I. Saloutin // Russian Journal of Applied Chemistry. - 2010. - Vol. 83, № 4. - P723-727 : табл., граф. - Bibliogr. : p. 723-727 (24 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
POLYMERS -- EPOXY-ANHYDRIDE POLYMERS -- OXIRANES -- POLYFLUOROLAKYL-SUBSTITUTED OXIRANES -- CURING
Аннотация: Epoxy-anhydride polymers based on N,N,O-triglycidyl-p-aminophenol and isomethyltetrahydrophthalic anhydride were synthesized in the presence of new active modifiers, polyfluoroalkyl glycidyl ethers. The kinetics of the reactions of the modifiers with the anhydride were studied by differential scanning calorimetry and IR spectroscopy. The physicomechanical characteristics, glass transition points, and water absorption of the polymers were determined.

\\\\Expert2\\nbo\\Russian Journal of Applied Chemistry\\2010, v. 83, N 4, p.723-727.pdf
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19.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis and properties of new π-conjugated imidazole/carbazole structures / R. A. Irgashev, N. A. Kazin, N. I. Makarova, I. V. Dorogan, V. V. Malov, A. R. Tameev, G. L. Rusinov, A. V. Metelitsa, V. I. Minkin, V. N. Charushin // Dyes and Pigments. - 2017. - Vol. 141. - P512-520
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
IMIDAZOLES -- CARBAZOLES -- ABSORPTION SPECTRA -- PHOTOLUMINESCENCE -- TDDFT CALCULATIONS -- CHARGE MOBILITY
Аннотация: New 3-(1H-imidazol-2-yl)-9H-carbazoles and 6,6′-di(1H-imidazol-2-yl)-9H,9′H-3,3′-bicarbazoles have been prepared, starting from 9-ethyl-9H-carbazole-3-carbaldehyde or 9,9′-diethyl-9H,9′H-[3,3′-bicarbazole]-6,6′-dicarbaldehyde through their reactions with 4-methoxyaniline or 4-fluoroaniline, benzil or 2,2′-thenil [1,2-di(thien-2,2′-yl) glyoxal] and ammonium acetate on reflux in glacial acetic acid. The obtained compounds have been shown to demonstrate an effective fluorescence in the blue spectral region, exhibiting quantum yields in the range of 0.08–0.51, depending on their molecular structure and solvent polarity. The nature of the observed absorption spectra has been elucidated by the TDDFT calculations.

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20.
Инвентарный номер: нет.
   
   S 98

   
    Synthesis of cyclometallated platinum complexes with substituted thienylpyridines and detailed characterization of their luminescence properties [Text] / D. N. Kozhevnikov, V. N. Kozhevnikov, M. M. Ustinova, A. Santoro, D. W. Bruce, B. Koenig, T. Fisher, M. Zabel, H. Yersin // Inorganic Chemistry . - 2009. - Vol. 48, № 9. - P4179-4189
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Synthesis of various derivatives of 2-(2-thienyl)pyridine via substituted 3-thienyl-1,2,4-triazines is reported. The final step of the synthesis is a transformation of the triazine ring to pyridine in an aza-Diels-Alder-type reaction. The resulting 5-aryl-2-(2-thienyl)pyridines (HL1-HL4) and 5-aryl-2-(2-thienyl)cyclopenteno[c]pyridines (HL5-HL8) (with aryl = phenyl, 4-methoxyphenyl, 2-naphtyl, and 2-thienyl) were used as cyclometallating ligands to prepare a series of eight luminescent platinum complexes of the type [Pt(L)(acac)] (L = cyclometallating ligand, acac = acetylacetonato). X-ray single crystal structures of three complexes of that series, [Pt(L5)(acac)] = [Pt(5-phenyl- 2-(2-thienyl)cyclopenteno[c]pyridine)(acac)], [Pt(L6)(acac)] = [Pt(5-(4-methoxy)-2-(2-thienyl)cyclopenteno[c]py- ridine)(acac)], and [Pt(L7)(acac)] = [Pt(5-(2-naphtyl)-2-(2-thienyl) cyclopenteno[c]pyridine)(acac)] were determined. Photoluminescence and electronic absorption spectra of the new [Pt(L)(acac)] complexes are reported. For two representative compounds of that series, [Pt(L4)(acac)] and [Pt(L5)(acac)], a detailed photophysical characterization based on highly resolved emission and excitation spectra, as well as on emission decay properties, was carried out. The studies down to low temperature (T = 1.2 K) and up to high magnetic fields (6 = 10 T) allowed us to characterize the three individual substates of the emitting triplet state. In particular, it is shown that the lowest triplet states of [Pt(L4)(acac)] and [Pt(L5)(acac)] are largely ligand-centered (LC) of3jtjt*character, which experience only weak spin- orbit couplings to higher lying singlet states

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