排序方式: 共有64条查询结果,搜索用时 31 毫秒
1.
L. G. Shaidarova S. A. Ziganshina G. K. Budnikov 《Journal of Analytical Chemistry》2003,58(6):577-582
The electrocatalytic activity of ruthenium(IV) oxide incorporated into a carbon-paste electrode was studied in the oxidation of cysteine and cystine. The oxidation potentials of the amino acids decreased and the current peaks of their oxidation increased at a modified electrode as compared to an unmodified one. Procedures for the voltammetric determination of cysteine and cystine with the use of electrodes chemically modified with ruthenium(IV) oxide were proposed. 相似文献
2.
L. G. Shaidarova S. A. Ziganshina L. N. Tikhonova G. K. Budnikov 《Journal of Analytical Chemistry》2003,58(12):1144-1150
The electrochemical behavior of sulfur-containing amino acids (cysteine, cystine, and methionine) at graphite electrodes modified with a ruthenium(III) hexacyanoferrate(II) film was studied. Glassy carbon and carbon paste were used as graphite materials. The electrocatalytic oxidation of amino acids at a modified electrode resulted in a decrease in the oxidation potentials of amino acids and an increase in the currents of their oxidation peaks as compared to those observed at an unmodified electrode. The voltammetric characteristics and hydrodynamic conditions for detecting the maximum catalytic current were found. A procedure is proposed for the electrocatalytic determination of cysteine, cystine, and methionine at a carbon-paste electrode modified with an inorganic film of ruthenium(III) hexacyanoferrate(II) under the conditions of flow-injection analysis. 相似文献
3.
Nazarov A. M. Khursan S. L. Kalinichenko I. A. Ziganshina S. Kh. Komissarov V. D. 《Kinetics and Catalysis》2002,43(4):459-464
The rate constants of the reactions of diphenyl carbonyl oxide Ph2COO with a number of alcohols and water in acetonitrile, benzene, andn-decane solutions (295 K) were measured by flash photolysis. The rate constants vary over a range from 400 (triphenylmethanol in a MeCN solution) to 2.5 × 105 l mol–1 s–1 (adamantanol in a benzene solution). -Methoxydiphenylmethyl hydroperoxide is the reaction product of Ph2COO and MeOH. The absence of a kinetic isotope effect and the dependence of the logarithms of the rate constants on the first ionization potentials of alcohols are indicative of the formation of a C–O bond at the rate-limiting step of the reaction. 相似文献
4.
V. V. Yanilkin A. R. Mustafina A. S. Stepanov N. V. Nastapova G. R. Nasybullina A. Yu. Ziganshina S. E. Solovieva A. I. Konovalov 《Russian Journal of Electrochemistry》2011,47(10):1082-1090
The results of authors on designing electroswitchable supramolecular systems based on calix[4]arenes, calix[4]resorcinols,
and transition metal ions and complexes are summarized. We consider systems in which the switching is performed owing to electrochemical
reactions both of groups grafted to the macrocycle and bound substrates. Examples of electrochemically switchable luminescence
are given. 相似文献
5.
Averko-Antonovich I. Yu. Ziganshina L. R. Rakhmatullina A. P. Akhmed'yanova R. A. 《Russian Journal of Applied Chemistry》2004,77(4):595-598
The surface activity of sodium, potassium and, ammonium salts of fatty acids [stearic, oleic, synthetic fatty acids (C1
3-C1
5 fractions), higher fatty acids contained in bottoms after separation of volatile fatty acids from cotton oil] in aqueous solutions was studied and analyzed. 相似文献
6.
Ana Santos‐Coquillat Enrique Martínez‐Campos Nelson Vargas‐Alfredo Raúl Arrabal Juan Rodríguez‐Hernndez Endzhe Matykina 《Macromolecular bioscience》2019,19(10)
Magnesium‐based implants present several advantages for clinical applications, in particular due to their biocompatibility and degradability. However, degradation products can affect negatively the cell activity. In this work, a combined coating strategy to control the implant degradation and cell regulation processes is evaluated, including plasma electrolytic oxidation (PEO) that produces a 13 µm‐thick Ca, P, and Si containing ceramic coating with surface porosity, and breath figures (BF) approach that produces a porous polymeric poly(ε‐caprolactone) surface. The degradation of PCL‐PEO‐coated Mg hierarchical scaffold can be tailored to promote cell adhesion and proliferation into the porous structure. As a result, cell culture can colonize the inner PEO‐ceramic coating structure where higher amount of bioelements are present. The Mg/PEO/PCL/BF scaffolds exhibit equally good or better premyoblast cell adhesion and proliferation compared with Ti CP control. The biological behavior of this new hierarchical functionalized scaffold can improve the implantation success in bone and cardiovascular clinical applications. 相似文献
7.
V. V. Yanilkin N. V. Nastapova R. R. Fazleeva G. R. Nasretdinova E. D. Sultanova A. Yu. Ziganshina A. T. Gubaidullin A. I. Samigullina V. G. Evtugin V. V. Vorobev Yu. N. Osin 《Russian Chemical Bulletin》2018,67(2):215-229
Efficient mediated electrosynthesis of nanocomposite Au@р(MVCA8+-co-St) (~6 nm), in which ultrasmall Au nanoparticles (Au-NP) were bound in nanocapsules of water-soluble nanoparticles of соpolymer р(MVCA8+-co-St) of tetraviologen calix[4]resorcinol (MVCA8+) with styrene (St), was accomplished by the reduction of AuI in aqueous medium. The quanti- tative reduction of AuI was carried out using the theoretically necessary amount of electricity and was not accompanied by the deposition of metal on the electrode. Radical cations of viologen units MV?+ of the molecule р(MVCA4?+-co-St) adsorbed on the electrode and π-dimers MV?+···MV?+ of π-polymers [р(MVCA4?+-co-St)] n deposited on the electrode act- ed as the reducing agents with respect to AuI. During electrolysis, the nanoparticles agglo- merated to 37—50 nm. The nanocomposite particles dispersed in ethanol had sizes of 72±16 nm and also contained Au-NP with sizes of 51±8 and 19±3 nm. The catalytic activity of the nanocomposite in the reduction of p-nitrophenol with sodium borohydride was demon- strated. A similar reduction of AgCl nanoparticles (~250 nm) led to the formation of silver nanoparticles with crystallite sizes in the range of 7—11 nm, the process was inefficient, however, even when using 250% of electricity, an incomplete reduction of AgCl was still observed. 相似文献
8.
Synthesis and antiadrenergic properties of β-substituted alcohols based on 6-hydroxymethylpyridoxine
R. S. Pavelyev R. R. Khairullina S. A. Koshkin A. G. Iksanova O. A. Lodochnikova N. N. Khaertdinov G. F. Sitdikova A. F. Safina E. G. Aleksandrova L. E. Ziganshina Yu. G. Shtyrlin 《Russian Chemical Bulletin》2016,65(2):519-531
An approach to the synthesis of epoxides based on 6-hydroxymethylpyridoxine acetals was developed. The epoxides obtained were involved in the ring opening reactions by nitrogen-, oxygen-, and sulfur-containing nucleophiles. Cytotoxicity and antiadrenergic properties of some synthesized compounds were studied on the models in situ and in vivo. 相似文献
9.
G. R. Nasybullina V. V. Yanilkin N. V. Nastapova A. Yu. Ziganshina D. E. Korshin Yu. S. Spiridonova A. A. Karasik A. I. Konovalov 《Russian Chemical Bulletin》2012,61(12):2295-2310
Binding of an amphiphilic dianion 1,5-bis(p-sulfonatophenyl)-3,7-diphenyl-1,5-diaza-3,7-diphosphacyclooctane (APCO2?) with an amphiphilic octacation tetra(methyl viologen) calix[4]resorcinol (MVCA8+) in media containing different amounts of water and DMSO using NaClO4 or NaCl as supporting electrolytes was shown for the first time by cyclic voltammetry and spectrophotometry. The stoichiometry of the complex depends on the MVCA8+: APCO2? ratio, medium, and supporting electrolyte. A 1: 1 charge-transfer complex is mainly formed (λmax = 480 nm) in 30% DMSO at a ratio of the compounds of 1: 1. A similar 1: 1 complex of APCO2? with a model compound methyl viologen MV2+ (λmax = 482 nm) is formed under these conditions. A donor-acceptor interaction occurs between the acceptor viologen units and nitrogen-centered electron-donating fragments of the APCO2? dianion. An increase in the content of APCO2? in the solution leads to an additional binding of one (30 vol.% DMSO, water, NaClO4) or two (30 vol.% DMSO, water, NaCl) particles of APCO2? with the hydrophobic fragments of MVCA8+. The complexes aggregate to form insoluble precipitates in aqueous and water-DMSO media. A selective reversible electroswitching from the bound to free state of one of the three bound APCO2? particles was performed when reducing MVCA8+ to MVCA4·+ in a 30 vol.% DMSO/NaCl medium. 相似文献
10.
Yanilkin Vitaliy V. Fazleeva Rezeda R. Nasretdinova Gulnaz R. Osin Yury N. Gubaidullin Aidar T. Ziganshina Аlbina Yu 《Journal of Solid State Electrochemistry》2020,24(4):829-842
Journal of Solid State Electrochemistry - Efficient two-step electrosynthesis of xCoO–yCo(OH)2 (CoOxHy)-supported silver nanoparticles (AgNPs) is carried out in N,N-dimethylformamide (DMF)... 相似文献