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Archive for A. Grevtsev

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.

July

Total in July 1187 service applications were carried out.
All together measured:

  • 1128 1H spectra
  • 232 13C spectra
  • 108 DEPT spectra
  • 10 COSY spectra
  • 10 NOESY spectra
  • 51 31P spectra
  • 19 19F spectra

165 applications were carried out.

MRI

picture sourse: www.independent.co.uk

Functional MRI (fMRI) is 25 years old, yet surprisingly its most common statistical methods has not been properly validated. A recent study published in PNAS has found that that the most common software packages for fMRI analysis can result in false-positive rates of up to 70% instead of expected 5%. These results question the validity of some 40,000 fMRI studies and may have a large impact on the interpretation of neuroimaging results.

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.

CMR users activity

Сертификат Organic Chemistry (1) Сертификат Physical Organic Chemistry Сертификат General and Inorganic Chemistry
CMR users continue to delight us with high activity. Three of the most active departments awarded honorary certificates. Designated as follows:

  • Department of Organic Chemistry – 25000 applications
  • Department of Physical Organic Chemistry – 10000 applications
  • Department of general and inorganic chemistry – 3000 applications

High-level


Sometimes our staff carry out the high-level service works.

June

Total in June 1317 service applications were carried out.
All together measured:

  • 1270 1H spectra
  • 210 13C spectra
  • 89 DEPT spectra
  • 14 COSY spectra
  • 14 NOESY spectra
  • 50 31P spectra
  • 56 19F spectra

159 applications were carried out.

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.

Guests from Alma-Ata

Excursion was carried out for masters students from Alma-Ata in CMR.