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Vladimir V. Klochkov

Researcher at Kazan Federal University

Publications -  207
Citations -  1630

Vladimir V. Klochkov is an academic researcher from Kazan Federal University. The author has contributed to research in topics: Nuclear magnetic resonance spectroscopy & Two-dimensional nuclear magnetic resonance spectroscopy. The author has an hindex of 18, co-authored 191 publications receiving 1221 citations. Previous affiliations of Vladimir V. Klochkov include Russian Academy of Sciences.

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Hydrothermal upgrading of heavy oil in the presence of water at sub-critical, near-critical and supercritical conditions

TL;DR: In this article, the authors investigated the performance of high sulfur-content heavy oil at sub-critical, near-critical and supercritical water (SCW) conditions, and showed that a viscosity reduction from 2073 to 1758mPa was achieved with a slight removal of sulfur (mainly sulfur) and the generation of a small amount of light and non-condensable hydrocarbons in gas phase (C1−C4, isoalkanes and alkenes, H2S, CO2 and H2, etc.).
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Application of high resolution NMR (1H and 13C) and FTIR spectroscopy for characterization of light and heavy crude oils

TL;DR: In this article, high-resolution nuclear magnetic resonance (NMR) and Fourier transform infrared (FTIR) spectroscopy experiments were applied to obtain detailed information on the hydrocarbon chemistry of three light and three heavy crude oils.
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Interaction of statins with phospholipid bilayers studied by solid-state NMR spectroscopy.

TL;DR: Investigation of the influence of the investigated statins on membrane structure revealed that lovastatin had the least effect on lipid packing and chain order, pravastatin significantly lowered lipid chain Order, while the other statins slightly decreased lipid chain order parameters mostly in the middle segments of the phospholipid chains.
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Determination of preferred conformations of ibuprofen in chloroform by 2D NOE spectroscopy.

TL;DR: Solution of an anti-inflammatory drug ibuprofen ((RS)-2-(4-isobutylphenyl) propionic acid) in chloroform was studied by nuclear magnetic resonance spectroscopy and three models of averaging were concerned to determine the dominant conformers of ib uprofen dissolved inchloroform.
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Spatial structure of cyclosporin A and insight into its flexibility

TL;DR: In this article, the authors used nuclear Overhauser effect (NOE) spectroscopy and analysis of residual dipolar couplings to obtain data on the molecular structure of dominant conformers of cyclosporin A.