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Complex formation of FeIII, CuII, and ZnII with L-3-(3,4-dihydroxyphenyl)alanine in aqueous solutions
Amirov R., Mingazova A., Ziyatdinova A., Zhuravleva Y., Solodov A.
magnetic relaxa- tion. The spectral and magnetic relaxation parameters of the L-3-(3,4-dihydroxyphenyl
Complex formation of FeIII, CuII, and ZnII with L-3-(3,4-dihydroxyphenyl)alanine in aqueous solutions
Amirov R., Mingazova A., Ziyatdinova A., Zhuravleva Y., Solodov A.
magnetic relaxa- tion. The spectral and magnetic relaxation parameters of the L-3-(3,4-dihydroxyphenyl
Study of molecular mobility in oligosulphones using pulsed NMR
Pestryayev Y., Storozhuk I.
Study of molecular mobility in oligosulphones using pulsed NMR
Determination of SARA fractions of crude oils by NMR technique
Verşan Kök M., Varfolomeev M., Nurgaliev D.
resonance spectroscopy (H NMR and C NMR) determinations. The hydrogen and carbon aromaticity factors were
Crystallisation of crystallizable and amorphous polymer mixtures and peculiarities of their structure: An NMR study
Filippov A., Smirnov V., Doroginizkij M.
magnetic resonance relaxation and nuclear magnetic resonance (NMR) with pulsed field gradient. The temporal
Supramolecular complex formed by DNA oligonucleotide and thiacalix[4]arene. NMR-spectroscopy and molecular docking
Khairutdinov B., Ermakova E., Sitnitsky A., Stoikov I., Zuev Y.
The combination of NMR-spectroscopy and molecular docking was applied to investigate
Nuclear magnetic resonance in dilute magnetic alloys and superconductors
Fazleev N., Mironov G.
Kondo systems are calculated. It is shown that obsevation of the Kondo anomalies in the NMR parameters
Structural studies of pravastatin and simvastatin and their complexes with SDS micelles by NMR spectroscopy
Rakhmatullin I., Galiullina L., Klochkova E., Latfullin I., Aganov A., Klochkov V.
and in their complexes with sodium dodecyl sulfate micelles (SDS) were studied by 2D NOESY NMR spectroscopy. On the basis
NMR determination of damaged layer thickness in the γ-irradiated polyethylene
Belousova M., Maklakov A., Skirda V., Bykov Y., Romanov B.
) and the total dose have been determined. This was done either by NMR measurements or by measuring self
Conformational stability of diastereomeric 8,8-dichloro-3,5-dioxa-4-thia-4-oxobicyclo[5.1.0]octanes: X-ray crystallography, dynamic 1H and 13C NMR spectroscopy study
Gavrilov V., Shamsutdinov M., Kataeva O., Klochkov V., Litvinov I., Shtyrlin Y., Klimovitskii E.
moiety and axial or equatorial sulfinyl group. Dynamic 1H and 13C NMR spectroscopy at -95 °S

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