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Archive for Acknowledging publications

ACS Catal., 2016, 6, 3637−3643

Y.S. Panova, A.S. Kashin, M.G. Vorobev, E.S. Degtyareva, V.P. Ananikov

“Nature of the Copper-Oxide-Mediated C−S Cross-Coupling Reaction: Leaching of Catalytically Active Species from the Metal Oxide Surface”

ACS Catal., 2016, 6, 3637−3643
DOI:10.1021/acscatal.6b00337

source: http://pubs.acs.org/doi/abs/10.1021/acscatal.6b00337

Copper-oxide-catalyzed cross-coupling reaction is a well-known strategy in heterogeneous catalysis. A large number of applications have been developed, and catalytic cycles have been proposed based on the involvement of the copper oxide surface. In the present work, we have demonstrated that copper(I) and copper(II) oxides served as precursors in the coupling reaction between thiols and aryl halides, while catalytically active species were formed upon unusual leaching from the oxide surface. A powerful cryo-SEM technique has been utilized to characterize the solution-state catalytic system by electron microscopy. A series of different experimental methods were used to reveal the key role of copper thiolate intermediates in the studied catalytic reaction. The present study shows an example of leaching from a metal oxide surface, where the leaching process involved the formation of a metal thiolate and the release of water. A new synthetic approach was developed, and many functionalized sulfides were synthesized with yields of up to 96%, using the copper thiolate catalyst. The study suggests that metal oxides may not act as an innocent material under reaction conditions; rather, they may represent a source of reactive species for solution-state homogeneous catalysis.

Carbohydrate Polymers, 2016, 151, 1152-1161

N.G. Voron’ko, S.R. Derkach, M.A. Vovk, P.M. Tolstoy

“Formation of -carrageenan–gelatin polyelectrolyte complexes studied by 1H NMR, UV spectroscopy and kinematic viscosity measurements”

Carbohydrate Polymers, 2016, 151, 1152-1161
DOI:10.1016/j.carbpol.2016.06.060

The intermolecular interactions between an anionic polysaccharide from the red algae κ-carrageenan and a gelatin polypeptide, forming stoichiometric polysaccharide–polypeptide (bio)polyelectrolyte complexes in the aqueous phase, were examined. The major method of investigation was high-resolution 1H NMR spectroscopy. Additional data were obtained by UV absorption spectroscopy, light scattering dispersion and capillary viscometry. Experimental data were interpreted in terms of the changing roles of electrostatic interactions, hydrophobic interactions and hydrogen bonds when κ-carrageenan–gelatin complexes are formed. At high temperatures, when biopolymer macromolecules in solution are in the state of random coil, hydrophobic interactions make a major contribution to complex stabilization. At the temperature of gelatin’s coil → helix conformational transition and at lower temperatures, electrostatic interactions and hydrogen bonds play a defining role in complex formation. A proposed model of the κ-carrageenan–gelatin complex is discussed.

Transition Met. Chem., 2016, 41, 387–392

A.M. Afanasenko, E.Yu. Bulatov, T.G. Chulkova, M. Haukka, F.M. Dolgushin

“An efficient method for selective oxidation of (oxime)Pt(II) to (oxime)Pt(IV) species using N,N-dichlorotosylamide”

Transition Met. Chem., 2016, 41, 387–392
DOI:10.1007/s11243-016-0034-7

The oxidation of (oxime)PtII species using the electrophilic chlorine-based oxidant N,N-dichlorotosylamide (4-CH3C6H4SO2NCl2) was studied. The reactions of trans-[PtCl2(oxime)2] (where oxime = acetoxime, cyclopentanone oxime, or acetaldoxime) with this oxidant led to trans-[PtCl4(oxime)2] products. The oxidation of trans-[Pt(o-OC6H4CH = NOH)2] at room temperature gave trans-[PtCl2(o-OC6H4CH = NOH)2], whereas the same reaction upon heating was accompanied by electrophilic substitution of the benzene rings.

J. Chem. Phys., 2016, 144, 224201

A.A. Shmyreva, M. Safdari, I. Furó, S.V. Dvinskikh

“NMR longitudinal relaxation enhancement in metal halides by heteronuclear polarization exchange during magic-angle spinning”

J. Chem. Phys., 2016, 144, 224201
DOI:10.1063/1.4953540

Orders of magnitude decrease of 207Pb and 199Hg NMR longitudinal relaxation times T 1 upon magic-angle-spinning (MAS) are observed and systematically investigated in solid lead and mercury halides MeX2 (Me = Pb, Hg and X = Cl, Br, I). In lead( ii) halides, the most dramatic decrease of T 1 relative to that in a static sample is in PbI2, while it is smaller but still significant in PbBr2, and not detectable in PbCl2. The effect is magnetic-field dependent but independent of the spinning speed in the range 200–15 000 Hz. The observed relaxation enhancement is explained by laboratory-frame heteronuclear polarization exchange due to crossing between energy levels of spin-1/2 metal nuclei and adjacent quadrupolar-spin halogen nuclei. The enhancement effect is also present in lead-containing organometal halide perovskites. Our results demonstrate that in affected samples, it is the relaxation data recorded under non-spinning conditions that characterize the local properties at the metal sites. A practical advantage of fast relaxation at slow MAS is that spectral shapes with orientational chemical shift anisotropy information well retained can be acquired within a shorter experimental time.

J. Org. Chem., 2016, 81, 5032-5045

M.A. Sandzhieva, A.N. Kazakova, I.A. Boyarskaya, A.Yu. Ivanov, V.G. Nenajdenko, A.V. Vasilyev

“Friedel–Crafts Alkylation of Arenes with 2-Halogeno-2-CF3-styrenes under Superacidic Conditions. Access to Trifluoromethylated Ethanes and Ethenes”

J. Org. Chem., 2016, 81, 5032-5045
DOI:10.1021/acs.joc.6b00419

The formation of the corresponding benzyl cations [ArHC+–CH(X)CF3] takes place under protonation of E-/Z-2-halogeno-2-CF3 styrenes [ArCH═C(X)CF3, X = F, Cl, Br] in superacids. The structures of these new electrophiles were studied by means of NMR and theoretical DFT calculations. According to these data, in the case of bromo derivatives, the formed cations, most probably, exist as cyclic bromonium ions; however, in the cases of chloro and fluoro derivatives, open forms are more preferable. Subsequent reaction of these benzyl cations with arenes proceeds as Friedel–Crafts alkylation to afford 1,1-diaryl-2-halo-3,3,3-trifluoropropanes [Ar(Ar′)CH–CH(X)CF3] in high yields (up to 96%) as a mixture of two diastereomers. The prepared halogenopropanes were easily converted into the corresponding mixtures of E-/Z-trifluoromethylated diarylethenes [Ar(Ar′)C═CCF3] (in yields up to 96%) by dehydrohalogenation with base (KOH or t-BuOK). The mechanism of elimination (E2 and Ecb) depends on the nature of the leaving group and reaction conditions.

Glass Physics and Chemistry, 2016, 42(3), 230–237

A.A. Osipov, V.E. Eremyashev, A.S. Mazur, P.M. Tolstoi, L.M. Osipova

“Coordination State of Aluminum and Boron in Barium Aluminoborate Glass”

Glass Physics and Chemistry, 2016, 42(3), 230–237
DOI:10.1134/S1087659616030111

This paper considers the coordination state of boron and aluminum ions in barium aluminoborate glass with a constant ratio of BaO : B2O3 = 0.5 and a variable ratio of Al2O3 : BaO = 0–3. The dependence of the concentrations of boron and aluminum atoms with a variable coordination number on the Al2O3 content was estimated by IR, 11B and 27Al NMR spectroscopy. The nonlinear nature of the obtained dependences was attributed to variations in the aluminum oxide properties. At a content of less than 30 mol % Al2O3 serves primarily as a network former, while an increase in the Al2O3 concentration results in its higher modifying role in the studied glass.

Russ. J. Gen. Chem., 2016, 85(11), 2541-2546

S.A. Kras’ko, S.S. Zlotskii, V.P. Boyarskii

“Comparative Activity of Aryl, Alkyl, and Cycloalkyl Halides in the Suzuki Reaction Catalyzed with Acyclic Diaminocarbene Complex of Palladium”

Russ. J. Gen. Chem., 2016, 85(11), 2541-2546
DOI:10.1134/S1070363215110079

Relative activity of halogenated arenes, alkanes, and alkanes in the Suzuki reaction catalyzed with acyclic diaminocarbene complex of palladium has been investigated. Under all the investigated conditions, 4-iodoanisole has been more active than the alkyl halides. The reaction with 4-methyl-1-(chloromethyl)benzene has afforded the target 4-methyl-1-(phenylmethyl)benzene along with significant amount of by-products; other alkyl and cycloalkyl halides do not participate into the cross-coupling reaction. Ethanol has been found the most suitable solvent for the reaction. The reaction in acetonitrile provides noticeable yield of the products only in the presence of polyethylene glycol and water.

Separation Sci. Tech., 2016, 51(7), 1103-1111

D.N. Konshina, V.V. Open’ko, Z.A. Temerdashev, A.A. Gurinov, V.V. Konshin

“Synthesis of novel silica-gel-supported thiosemicarbazide and its properties for solid phase extraction of mercury”

Separation Sci. Tech., 2016, 51(7), 1103-1111
DOI:10.1080/01496395.2016.1143005

A new thiosemicarbazidе-modified silica gel (SG-THSC) sorbent was prepared. The sorbent was quantified by adsorption of mercury ions on silica gel, desorption and then spectrophotometry detection of mercury ions. The retention parameters (sample flow rate, eluent type, sample volume, presence of foreign ions, shaking time, sample flow rate and volume, eluent condition, interfering substances) were investigated. The quantitative recovery (>95%) of Hg(II) ions could be obtained by use of 5 mL of 6 mol L−1 HCl. The adsorption capacity of SG-THSC was found to be 98.3 mg g–1 at optimum pH. The maximum preconcentration factor was 400. The technique detection limit was 70 ng L–1, and the relative standard deviation was lower than 4.0% (n = 6). The studied sorbent was applied to preconcentrate the trace Hg(II) from the mineralised residues of fish and seawater samples.

Sci. Rep., 2016, 6, 24270

D.A. Markelov, V.V. Matveev, P. Ingman, M.N. Nikolaeva, A.V. Penkova, E. Lahderanta, N.I. Boiko, V.I. Chizhik

“Unexpected Temperature Behavior of Polyethylene Glycol Spacers in Copolymer Dendrimers in Chloroform”

Sci. Rep., 2016, 6, 24270
DOI:10.1038/srep24270

We have studied copolymer dendrimer structure: carbosilane dendrimers with terminal phenylbenzoate mesogenic groups attached by poly(ethylene) glycol (PEG) spacers. In this system PEG spacers are additional tuning to usual copolymer structure: dendrimer with terminal mesogenic groups. The dendrimer macromolecules were investigated in a dilute chloroform solution by 1H NMR methods (spectra and relaxations). It was found that the PEG layer in G = 5 generations dendrimer is “frozen” at high temperatures (above 260 K), but it unexpectedly becomes “unfrozen” at temperatures below 250 K (i.e., melting when cooling). The transition between these two states occurs within a small temperature range (~10 K). Such a behavior is not observed for smaller dendrimer generations (G = 1 and 3). This effect is likely related to the low critical solution temperature (LCST) of PEG and is caused by dendrimer conformations, in which the PEG group concentration in the layer increases with growing G. We suppose that the unusual behavior of PEG fragments in dendrimers will be interesting for practical applications such as nanocontainers or nanoreactors.

Beilstein J. Org. Chem., 2015, 11, 373-384

N.A. Danilkina, P.S. Vlasov, S.M. Vodianik, A.A. Kruchinin, Y.G. Vlasov, I.A. Balova

“Synthesis and chemosensing properties of cinnoline-containing poly(arylene ethynylene)s”

Beilstein J. Org. Chem., 2015, 11, 373-384
DOI:10.3762/bjoc.11.43

Novel poly(arylene ethynylene)s comprising a cinnoline core were prepared in high yields via a three-step methodology. A Richter-type cyclization of 2-ethynyl- and 2-(buta-1,3-diynyl)aryltriazenes was used for cinnoline ring formation, followed by a Sonogashira coupling for the introduction of trimethylsilylethynyl moieties and a sila-Sonogashira coupling as the polycondensation technique. The fluorescence of the cinnoline-containing polymers in THF was highly sensitive to quenching by Pd2+ ions.