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1.
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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2.
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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3.
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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4.
Инвентарный номер: нет.
   
   U 67

   
    Upconversion luminescence in Er3+/Yb3+ codoped Y2CaGe4O12 [Electronic resource] / I. I. Leonidov, V. G. Zubkov, A. P. Tyutyunnik, N. V. Tarakina, L. L. Surat, O. V. Koryakova, E. G. Vovkotrub // Journal of Alloys and Compounds. - 2011. - Vol. 509, № 5. - P1339-1346. - Bibliogr. : p. 1345-1346 (52 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: Calcium yttrium tetrametagermanates Y2CaGe4O12 doped with Er3+ and Er3+/Yb3+ reveal upconversion emission in visible spectral range under near-infrared excitation, ex = 980 nm. For the solid solution ErxY2?xCaGe4O12 concentration dependencies for the green and red lines of the visible emission around 526 nm (2H11/2 4I15/2), 545 nm (4S3/2 4I15/2) and 670 nm (4F9/2 4I15/2) show the optimal value for the sample x = 0.2. The power dependence of the visible luminescence measured at room temperature in the low-power limit indicates two-photon upconversion process. Direct intensification of the upconversion emission signals has been achieved by ytterbium sensitizing. The other upconversion excitation mechanism in Y2CaGe4O12:Er3+ is discussed for an 808 nm incident laser irradiation. A scheme of excitation and emission routes involving ground/excited state absorption, energy transfer upconversion, nonradiative multiphonon relaxation processes in trivalent lanthanide ions in Y2CaGe4O12:Er3+ and Y2CaGe4O12:Er3+, Yb3+ has been proposed. Conditions for visible emission occurrence under quasi-resonance ex = 1064 nm excitation depending on pump power values are considered. In the low-power regime only near-infrared emission caused by the transition 4I13/2 4I15/2 in erbium ions has been detected

\\\\Expert2\\nbo\\Journal of Alloys and Compounds\\2011, v.509, N 5, p.1339.pdf
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5.
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   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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6.
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   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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7.
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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8.
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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9.
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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10.
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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