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1.
Инвентарный номер: нет.
   


   
    Combination of fluorescent and spin labels: a powerful method for the optimization of hydrophilic membranes for the separation of oil-in-water emulsions / R. S. Alqubelat, A. D. Kuznetsova, D. O. Antonov, M. A. Mironov // Chimica Techno Acta. - 2023. - Vol. 10, № 4. - P202310415
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
FLUORESCENT LABEL -- SPIN LABEL -- OIL-IN-WATER EMULSION
Аннотация: A new method for assessing the quality of fibre coating based on a combination of fluorescence microscopy and electron paramagnetic resonance is presented in this work. An influence of the carboxymethylcellulose/polyvinylamine gel preparation method on the mobility of the spin label was established. The mobility of the spin label changes from 3.5 ns in the case of a polyvinylamine solution to 12.8 ns in the case of a cross-linked gel on the surface of the glass fibre. A qualitative relationship was found between the mobility of the spin label in the gel applied to the glass fibre and the rate of spreading of crude oil over its surface. This method can be used to make membranes for the separation of water-in-oil emulsions.

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2.
Инвентарный номер: нет.
   


    Joy, M. N.
    Suzuki coupling in water: facile synthesis of novel coumarins / M. N. Joy, G. V. Zyryanov, S. Santra // Modern synthetic methodologies for creating drugs and functional materials (MOSM 2023) : book of abstracts of the 7th International conference. - Perm, 2023. - С. 72
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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3.
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    Synthesis of new water-soluble polyarene-substituted naphtho[1,2-d]oxazole-based fluorophores as fluorescent dyes and biological photosensitizers / N. V. Slovesnova, A. S. Minin, O. S. Taniya [et al.] // Dyes and Pigments. - 2022. - Vol. 204. - Ст. 110410
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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4.
Инвентарный номер: нет.
   


   
    Nanocomposite hydrogels for wastewater treatment / V. Madhavi, T. Ramesh, N. B. Reddy, G. V. Zyryanov // AIP conference proceedings. - 2022. - Vol. 2390. - Ст. 020043
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HYDROGELS -- NANOCOMPOSITES -- NANOTECHNOLOGY
Аннотация: The insufficient access to drinking water is one of the most prevailing problems throughout the world. It is highly essential for future demands to bring wastewater to reusable form. Hence, water purification has been the focus and attention of many scientists and governmental agencies. The combination of adsorption and nanotechnology-oriented approach with conventional treatment methods has offered interesting benefits to treat waste water. During the last decade, hydrogels have been used as potential adsorbents for the removal of different types of water pollutants. The combination of hydrogels and nanomaterials with multifunctional framework leads to the development of hybrid hydrogels that gives synergistic effect to the novel materials. Because of their biocompatibility and ability to mix with other materials, hydrogels coupled with versatile chemical groups with well-defined three-dimensional porous structure were potentially used for removal of toxic pollutants in water. This article briefly reviews the recent progress in nanobased hydrogels with particular emphasis on wastewater treatment applications.

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5.
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    Synthesis of δ-Valerolactone Using Stable Hydrogen Peroxide Derivatives / Y. V. Solovyova, A. V. Pestov, I. S. Puzyrev [et al.] // Russian Journal of Organic Chemistry. - 2022. - Vol. 58, № 4. - P480-483
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: The efficiencies of hydrogen peroxide derivatives in the Baeyer–Villiger oxidation of cyclopen­tanone to δ-valerolactone have been compared. The oxidants used were hydrogen peroxide in acetic, formic, or trifluoroacetic acid, magnesium and sodium monoperoxyphthalates, cumene hydroperoxide, and tert-butyl hydroperoxide. The oxidation was carried out in water, aqueous methanol, and water–ethyl acetate. Sodium and magnesium monoperoxyphthalates turned out to provide high conversion and selectivity under mild conditions.

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6.
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    Pyrene derivatives with peg-linker for the visual detection of nitro compounds in water / L. K. Sadieva, I. S. Kovalev, O. S. Taniya [et al.] // Современные синтетические методологии для создания лекарственных препаратов и функциональных материалов : сборник тезисов VI Международной конференции. - Екатеринбург, 2022. - Ст. II-31
Рубрики: ХИМИЧЕСКИЕ НАУКИ
   ЗДРАВООХРАНЕНИЕ. МЕДИЦИНСКИЕ НАУКИ


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7.
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    N-aminoacyl-3-amino-nido-carboranes as a group of boron-containing derivatives of natural amino acids / D. A. Gruzdev, A. A. Telegina, G. L. Levit, V. P. Krasnov // Journal of Organic Chemistry. - 2022. - Vol. 87, № 8. - P5437-5441
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Аннотация: A new group of nido-carboranyl derivatives of natural (S)-amino acids containing from 9 to 18 boron atoms was obtained in good yields as a result of acylation of 3-amino-1,2-dicarba-closo-dodecaborane followed by deboronation. The proposed approach is convenient and based on the use of readily available reagents and is suitable for the synthesis of enantiopure nido-carboranyl derivatives of amino acids with various side chains, including water-soluble boron-containing amino acids (17 examples).

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8.
Инвентарный номер: нет.
   
   D 46


   
    Design and antioxidant properties of bifunctional 2H-imidazole-derived phenolic compounds-a new family of effective inhibitors for oxidative stress-associated destructive processes / E. L. Gerasimova, E. R. Gazizullina, M. V. Borisova [et al.] // Molecules. - 2021. - Vol. 26, № 21. - Ст. 6534
ББК Г
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
2H-IMIDAZOLE -- POLYPHENOLS -- ANTIOXIDANT CAPACITY -- ANTIRADICAL CAPACITY
Аннотация: The synthesis of inhibitors for oxidative stress-associated destructive processes based on 2H-imidazole-derived phenolic compounds affording the bifunctional 2H-imidazole-derived phenolic compounds in good-to-excellent yields was reported. In particular, a series of bifunctional organic molecules of the 5-aryl-2H-imidazole family of various architectures bearing both electron-donating and electron-withdrawing substituents in the aryl fragment along with the different arrangements of the hydroxy groups in the polyphenol moiety, namely derivatives of phloroglucinol, pyrogallol, hydroxyquinol, including previously unknown water-soluble molecules, were studied. The structural and antioxidant properties of these bifunctional 5-aryl-2H-imidazoles were comprehensively studied. The redox transformations of the synthesized compounds were carried out. The integrated approach based on single and mixed mechanisms of antioxidant action, namely the AOC, ARC, Folin, and DPPH assays, were applied to estimate antioxidant activities. The relationship “structure-antioxidant properties” was established for each of the antioxidant action mechanisms. The conjugation effect was shown to result in a decrease in the mobility of the hydrogen atom, thus complicating the process of electron transfer in nearly all cases. On the contrary, the conjugation in imidazolyl substituted phloroglucinols was found to enhance their activity through the hydrogen transfer mechanism. Imidazole-derived polyphenolic compounds bearing the most electron-withdrawing functionality, namely the nitro group, were established to possess the higher values for both antioxidant and antiradical capacities. It was demonstrated that in the case of phloroglucinol derivatives, the conjugation effect resulted in a significant increase in the antiradical capacity (ARC) for a whole family of the considered 2H-imidazole-derived phenolic compounds in comparison with the corresponding unsubstituted phenols. Particularly, conjugation of the polyphenolic subunit with 2,2-dimethyl-5-(4-nitrophenyl)-2H-imidazol-4-yl fragment was shown to increase ARC from 2.26 to 5.16 (104 mol-eq/L). This means that the considered family of compounds is capable of exhibiting an antioxidant activity via transferring a hydrogen atom, exceeding the activity of known natural polyphenolic compounds.

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9.
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    Synthesis, characterization, and in vitro assessment of cytotoxicity for novel azaheterocyclic nido-carboranes – Candidates in agents for boron neutron capture therapy (BNCT) of cancer / M. V. Varaksin, L. A. Smyshliaeva, V. L. Rusinov [et al.] // Tetrahedron. - 2021. - Vol. 102. - P132525
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
AZAHETEROCYCLES -- BNCT -- CYTOTOXICITY -- CARBORANES
Аннотация: A series of novel water-soluble azaheterocyclic derivatives of nido-carborane bearing quinoxaline, 2H-imidazole or 1,2,4-triazine moieties were first synthesized in 82–91% yields. The structures of these boron-enriched compounds were confirmed by the data of NMR, IR spectroscopy, and mass spectrometry. To access the toxicity level for these organoboron compounds, the cytotoxicity indexes (IC50) were determined using by the MTT test on both human glioblastoma cell A-172 (IC50 = 150–243 μM) and human embryonic lung cells (IC50 = 424–944 μM) lines. The obtained preliminary results from in vitro analysis enable the synthesized water-soluble azaheterocyclic carboranes to be considered as challenging candidates in the design of agents for boron-neutron capture therapy (BNCT) of malignant tumors.

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10.
Инвентарный номер: нет.
   


   
    Synthesis of water-soluble gadolinium(iii) complexes based on 5-aryl-2,2′-bipyridine with a DTTA residue in position C6′ / A. P. Krinochkin, D. S. Kopchuk, Y. K. Shtaitz [et al.] // AIP Conference Proceedings. - 2021. - Vol. 2388, № 1. - Ст. 030017
Рубрики: ХИМИЧЕСКИЕ НАУКИ

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11.
Инвентарный номер: нет.
   


   
    Substituted 2-(2-hydroxyphenyl)–3H-quinazolin-4-ones and their difluoroboron complexes: Synthesis and photophysical properties / T. N. Moshkina, E. V. Nosova, V. N. Charushin [et al.] // Spectrochimica acta part A: molecular and biomolecular spectroscopy. - 2021. - Vol. 252. - P119497
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ESIPT -- FLUORESCENCE -- O-LIGAND -- BF2-COMPLEX2-(2-HYDROXYPHENYL)–3H-QUINAZOLIN-4-ONES
Аннотация: 2-(2-Hydroxyphenyl)–3H-quinazolin-4-ones with diverse substituents at phenol ring and their six-membered difluoroboron complexes have been synthesized via few-stage approach. The photophysical properties of target compounds have been investigated in two solvents as well as in the solid state. The nature of substituents and substitution point in the phenol moiety of ligands and resulting BF2-complexes on the photophysical properties of dyes have been explored. The complex bearing two t-Bu groups proved to be the most emissive in solid state, whereas its 5-methoxy and 4-diethylamino counterparts possess strong emission in toluene solution. The dyes exhibited large Stokes shifts which was attributed to excited state intramolecular proton transfer (ESIPT). Additionally, fluorescence of quinazolinones in the mixture of THF/water was studied. All ligands demonstrated emission enhancement with increase of water fraction which was due to aggregation induced emission.

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12.
Инвентарный номер: нет.
   


   
    Synthesis and physicochemical and catalytic properties of composites in the Sio2–Zro2 system / A. N. Murashkevich, O. A. Alisienok, E. S. Novik [et al.] // Inorganic materials. - 2020. - Vol. 56, № 4. - P430-436
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
ACID-BASE PROPERTIES -- CATALYSIS -- COMPOSITE -- SILICA -- SPECIFIC SURFACE AREA -- ZIRCONIA
Аннотация: Using coprecipitation, a sol–sol method, and molecular layering, we have synthesized SiO2–ZrO2 composites with SiO2 : ZrO2 ratios from 1 : 1 to 9 : 1 and a large specific surface area, which increases with growth silicon-containing component concentration. Using adsorption of Hammett indicators, we have assessed the concentration of acid–base centers in the pK range 1.3–9.6, which has been shown to vary from 68 to 160 μmol/g. Elemental analysis and IR spectroscopy data have demonstrated the presence of not only water but also nitrate ions and carbon dioxide on the surface of the samples. It has been shown that the use of nanoparticulate SiO2–ZrO2 oxides as heterogeneous catalysts—promoters for (2S,4R)-4-hydroxyprolyl-(S)-1-phenylethylamine trifluoroacetate, a chiral inducer in the asymmetric Biginelli reaction, makes it possible to raise ee (enantiomeric excess) from 39 to 68% and the reaction yield from 29 to 55%.

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13.
Инвентарный номер: нет.
   


    Tchaikovskaya, O.
    Kinetic model for UV/H2O2 degradation of 8-methoxypsoralen / O. Tchaikovskaya, N. Bryantseva, V. Krayukhina // Proceedings of SPIE - The International Society for Optical Engineering 13. Сер. "International Conference on Atomic and Molecular Pulsed Lasers XIII" . - Tomsk, 2018. - P1061422
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
8-METHOXYPSORALEN -- FUROCOUMARIN -- H2O2 -- IRRADIATING -- KRCL AND XEBR EXCILAMPS -- PHOTO-INDUCED DEGRADATION -- PUVA THERAPY
Аннотация: The influence of Crossed D sign?2Crossed D signz2 on the degradation of 8-methoxypsoralen (8-MOP) in water-ethanol solutions under the action of KrCl and XeBr excilamp radiation in a photoreactor is investigated. A kinematic model of photodegradation of the investigated molecule is constructed. In water-ethanol solutions the addition of Crossed D sign?2Crossed D signz2 altered the mechanism of decay of 8-MOP under the action of a KrCl excilamp in comparison with irradiation by a XeBr excilamp. This behavior is explained by the fact that the action of 283 nm radiation leads to accumulation of a stable photoproduct. In order to establish the toxicity of this product further research is needed.

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14.
Инвентарный номер: нет.
   
   F 70


   
    Fluorescent Detection of 2,​4-​DNT and 2,​4,​6-​TNT in Aqueous Media by Using Simple Water-​Soluble Pyrene Derivatives [Electronic resource] / I. S. Kovalev, O. S. Taniya, N. V. Slovesnova, G. A. Kim, S. Santra, G. V. Zyryanov, D. S. Kopchuk, A. Majee, V. N. Charushin, O. N. Chupakhin // Chemistry - An Asian Journal. - 2016. - Vol. 11, № 5. - С. 775-781
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HERBICIDES -- PYRENE DERIVATIVES
Аннотация: Pyrene-contg. water-sol. probes for the fluorescent detection of nitroarom. compds. (NACs), such as explosive components (2,4-DNT and 2,​4,​6-​TNT) and herbicides (2,4-​dinitrocresol, 2,4-DNOC)​, in aq. media are reported. In the probes, the introduction of surface-​active hydrophilic heads at the periphery of lipophilic (i.e., hydrophobic) pyrene tails resulted in the formation of highly fluorescent micelle-​like aggregates​/pre-​assocs. in aq. solns. at concns. of ≤10-5M. The enhanced fluorescence quenching of the herein reported architectures is achieved in the presence of ultra-​trace amts. of TNT or 2,4-DNT with values of Stern-​Volmer quenching const. close to 1 × 105M and a detection limit as low as 182 ppb. The most hydrophilic probes demonstrated higher response to 2,​4-​DNT over TNT. Filter paper test strips impregnated with 1 × 10-​5M solns. of the probes were able to detect TNT, 2,​4-​DNT, and other NACs at levels as low as 50 ppb in water.

\\\\expert2\\NBO\\Chemistry - an Asian Journal\\2016. 11(5). P. 775-781.pdf
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15.
Инвентарный номер: нет.
   
   R 74


   
    Role of polar solvents for the synthesis of pillar[6]arenes [Electronic resource] / S. Santra, I. S. Kovalev, D. S. Kopchuk, G. V. Zyryanov, A. Majee, V. N. Charushin, O. N. Chupakhin // RSC Advances. - 2015. - Vol. 5, № 126. - С. 104278-104282. - Bibliogr. : p. 104282 (26 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
HOST-GUEST COMPLEXATION -- WATER CHANNELS -- HIGH-YIELD SYNTHESIS
Аннотация: An efficient procedure for the synthesis of pillar[6]arenes has been developed. The procedure involves the condensation of 1,4-dialkoxybenzenes and paraformaldehyde in the presence of a catalytic amount of H2SO4 or BF3 center dot OEt2 in polar solvent media (acetonitrile, ethyl alcohol, acetone etc.). In all cases the interaction afforded pillar[6]arenes in high yields.

\\\\expert2\\nbo\\RSC Advances\\2015. Vol. 5, N 126. P. 104278-104282.pdf
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16.
Инвентарный номер: нет.
   
   F 33


   
    Features of silicon- and titanium-polyethylene glycol precursors in sol-gel synthesis of new hydrogels [Electronic resource] / T. G. Khonina, A. P. Safronov, M. V. Ivanenko, E. V. Shadrina, O. N. Chupakhin // Journal of Materials Chemistry B. - 2015. - Vol. 3, № 27. - С. 5490-5500. - Bibliogr. : p. 5499-5500 (38 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
MODIFIED SILANES -- MINERALIZATION -- MONOLITHS
Аннотация: The formation of organic/inorganic hydrogels based on silicon and titanium polyethylene glycolates, new biocompatible water-soluble precursors in sol-gel processing, was investigated. The influence of different factors on the gelation process, such as excess of PEG, water molar content, pH of medium, electrolyte additives, was investigated in comparison with silicon-and titanium-glycerol precursors. The specific features of gelation for each type of precursor were revealed. It has been determined that titanium polyethylene glycolates synthesized and used in the excess of PEG formed transparent polymeric hydrogels resistant to syneresis under certain conditions. The titanium polyethylene glycolates synthesized without excess of PEG formed turbid heterogeneous colloidal gels. In the case of silicon polyethylene glycolates the hydrogels obtained were polymeric. Dynamic light scattering was used to confirm the polymeric or colloidal type of gelation. The solid and liquid phases of polymeric silicon- and titanium-polyethylene glycol hydrogels were separated by exhaustive extraction. The solid phase was characterized by combined thermal analysis with simultaneous quadruple mass spectrometry, XRD, IR spectroscopy, and liquid phase-atomic emission spectroscopy. The structural features of polymeric gels were investigated by SEM and TEM methods. The cross-linking density of polymeric hydrogels was evaluated using Flory-Rehner theory based on the mechanical properties of swollen networks of flexible polymeric chains

\\\\expert2\\nbo\\Journal of Materials Chemistry B\\2015. V. 3, N 27. P. 5490-5500.pdf
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17.
Инвентарный номер: нет.
   
   M 85


   
    Morphology and Piezoelectric Properties of Diphenylalanine Microcrystals Grown from Methanol-Water Solution / P. S. Zelenovskiy, V. Ya. Shur, A. S. Nuraeva, S. G. Vasilev, D. S. Vasileva, D. O. Alikin, D. S. Chezganov, V. P. Krasnov, A. L. Kholkin // Ferroelectrics. - 2015. - Vol. 475, № 1. - С. 127-134
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
MORPHOLOGY PROPERTIES -- PIEZOELECTRIC PROPERTIES -- METHANOL-WATER SOLUTION

\\\\expert2\\NBO\\Ferroelectrics\\2015, v.475, N 1, p.127-134.pdf
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18.
Инвентарный номер: нет.
   
   B 12


   
    Bacterial degradation of a mixture obtained through the chemical modification of polychlorinated biphenyls by polyethylene glycols / D. O. Egorova, T. I. Gorbunova, M. G. Pervova, V. A. Demakov // Applied Biochemistry and Microbiology. - 2014. - Vol. 50, № 7. - С. 722-729. - Bibliogr. : p. 729 (29 ref.)
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
BACTERIAL DEGRADATION -- CHEMICAL MODIFICATION -- POLYETHYLENE GLYCOLS
Аннотация: Polychlorinated biphenyls (PCBs), also known by the trade name Sovol, are toxic industrial wastes. They have been subjected to chemical treatment by polyethylene glycols (PEGs) and potassium hydroxide. As a result of the interaction of the Sovol with various molecular mass PEGs (MMPEG-4 ∼ 200, MMPEG-22 ∼ 1000), water-soluble mixtures M1 and M2 containing mono(polyethylene glycol)oxy-derivatives (PCB-PEG-4 and PCB-PEG-22), polychlorobiphenylols, and unreacted PCB congeners (PCB 44, PCB 47, PCB 49, PCB 52, and PCB 66) were obtained. It was shown for the first time that mixtures M1 and M2 are susceptible to bacterial degradation without their fractionation. According to the gas-liquid chromatography with flame-ionization and mass-spectrometric detection, the Rhodococcus wratislaviensis KT112-7 strain degraded all of the chemical compounds occurring in the mixtures. In a 5-day experiment, it was found that the KT112-7 strain decomposes mono(polyethylene glycol)oxy-derivatives completely (by 100%) and polychlorobiphenylols and PCB congeners by 90–95% in the M1 and M2 mixtures. The culture medium did not contain transformation products, whereas free chlorine ions were accumulated (72–94% of the maximum possible amount). Thus, the use of the chemical modification and consecutive bacterial degradation provided an effective destruction of technical PCB mixtures with a high content of highly chlorinated congeners

\\\\expert2\\nbo\\Applied Biochemistry and Microbiology\\2014, v.50, N 7, p.722-729.pdf
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19.
Инвентарный номер: нет.
   
   P 41


   
    Pentacyanoferrate(II) complexes with N-containing derivatives of chitosan and polyallylamine: Synthesis and cesium uptake properties [Electronic resource] / S. YU. Bratskaya, V. V. Zheleznov, Y. O. Privar, A. Mechaev, A. V. Pestov // Colloids and Surfaces A: Physicochemical and Engineering Aspects. - 2014. - Vol. 460. - С. 145-150
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SODIUM AMINOPRUSSIDE -- POLYMER LIGANDS (CHITOSAN) -- POLYALLYLAMINE
Аннотация: Here we report on synthesis of new organic–inorganic materials based on products of interaction between sodium aminoprusside and polymer ligands (chitosan (CS), N-2-(2-pyridyl)ethylchitosan (2-PC), N-2-(4-pyridyl)ethylchitosan (4-PC), N-(4-methyl-5-imidazolyl)methylchitosan (IC), N-(2-cyanoethyl)chitosan (CC), polyallylamine (PA), N-(2-pyridyl)methyl-polyallylamine (PMPA), N-2-(2-pyridyl)ethyl-polyallylamine (PEPA), N-(4-methyl-5-imidazolyl)methyl-polyallylamine (IPA) and poly(2-vinylpyridine) (PVP)). The composition of the obtained materials was characterized using the element analysis and X-ray diffraction; the Fourier transform infrared (FT-IR) spectroscopy and thermogravimetric analysis data were used to propose the structure of the formed complexes. It was established that ion and ligand exchange were the main reactions, through which sodium aminoprusside interacts with water-soluble polymer salts. Reactivity in complex formation reaction of unmodified polymers changes in a row: PA > CS > PVP. Modification of chitosan with 2-(4-pyridyl)ethyl and 2-cyanoethyl moieties enhances reactivity of chitosan to the level of PA, while introduction of 2-(2-pyridyl) and (4-methyl-5-imidazolyl)methyl moieties, on the contrary, decreases reactivity of chitosan to that of PVP. At the same time, functionalization of PA with 2-pyridylalkyl groups decreases its reactivity in reaction with aminoprusside ion. Thus, reactivity of all studied polymeric matrices changes in the row: PA ≈ 4-PC ≈ CC > CS > 2-PC ≈ IPA ≈ IC > PMPA > PVP > PEPA. The distribution coefficients with respect to cesium ions have been determined for the synthesized complexes in cobalt(II) form. It has been shown that the complex of chitosan with pentacyanoferrate(II) has higher distribution coefficient with respect to Cs+ ions, as compared to its N-derivatives and synthetic polymers. Organic–inorganic materials obtained in the matrix of synthetic polymers have shown higher tendency to peptization and, therefore, lower sorption capacities and distribution coefficients

\\\\expert2\\nbo\\Colloids and Surfaces A\\2014, v.460, p.145-150.pdf
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20.
Инвентарный номер: нет.
   
   P 41


   
    Pentacyanoferrate(II) complexes with chitosan [Electronic resource] / S. YU. Bratskaya, Y. O. Privar, O. V. Korjakova, A. Mechaev, A. V. Pestov // Polymer Engineering and Science . - 2013. - Article in Press
ББК 54
Рубрики: ХИМИЧЕСКИЕ НАУКИ
Кл.слова (ненормированные):
SODIUM AMINOPRUSSIDE -- POLYMER LIGAND (CHITOSAN) -- X-RAY DIFFRACTION
Аннотация: New organic-inorganic materials based on products of interaction between sodium aminoprusside and polymer ligand (chitosan) have been synthesized. The composition of the obtained materials was characterized using the element analysis and X-ray diffraction; the Fourier transform infrared (FT-IR) spectroscopy and Thermogravimetric analysis data were used to propose the structure of the formed complexes. It was established that ion and ligand exchange were the main reactions at interaction of sodium aminoprusside with water-soluble chitosan salts. The comparative estimation of the sorption capacity with respect to cesium ions was performed for the synthesized complexes. It has been shown that the complex of chitosan with pentacyanoferrate(II) in the form of cobalt(II) salt has higher distribution coefficient with respect to Cs+ ions, as compared to cobalt aminoprusside. The maximum sorption capacity value for Cs+ was evaluated from the sorption isotherm and found to be equal to 0.3 mmol/g

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