48 results on '"Gurinov, Andrei"'
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2. From single-site tantalum complexes to nanoparticles of Ta x N y and TaO x N y supported on silica: elucidation of synthesis chemistry by dynamic nuclear polarization surface enhanced NMR spectroscopy and X-ray absorption spectroscopy
3. Unravelling potential reaction intermediates during catalytic pyrolysis of polypropylene with microscopy and spectroscopy
4. Correction: Unravelling potential reaction intermediates during catalytic pyrolysis of polypropylene with microscopy and spectroscopy
5. A site-sensitive quasi-in situ strategy to characterize Mo/HZSM-5 during activation
6. Unravelling potential reaction intermediates during catalytic pyrolysis of polypropylene with microscopy and spectroscopy.
7. NMR Spectroscopy Applied to Nanostructured Materials
8. Designing Highly Conductive Sodium-Based Metal Hydride Nanocomposites: Interplay between Hydride and Oxide Properties
9. A high-field cellular DNP-supported solid-state NMR approach to study proteins with sub-cellular specificity
10. A high-field cellular DNP-supported solid-state NMR approach to study proteins with sub-cellular specificity.
11. Designing Highly Conductive Sodium‐Based Metal Hydride Nanocomposites: Interplay between Hydride and Oxide Properties
12. Highly bioresistant, hydrophilic and rigidly linked trityl-nitroxide biradicals for cellular high-field dynamic nuclear polarization
13. Highly bioresistant, hydrophilic and rigidly linked trityl-nitroxide biradicals for cellular high-field dynamic nuclear polarization
14. Highly Efficient Trityl-nitroxide Biradicals for Biomolecular High-field Dynamic Nuclear Polarization
15. Surface enhanced dynamic nuclear polarization solid-state NMR spectroscopy sheds light on Brønsted–Lewis acid synergy during the zeolite catalyzed methanol-to-hydrocarbon process† †Electronic supplementary information (ESI) available: Complete experimental procedure, supplementary NMR figures and analysis. See DOI: 10.1039/c9sc02215e
16. In Vitro and in Vivo Studies on HPMA-Based Polymeric Micelles Loaded with Curcumin
17. Reaction Mechanism of Pd-catalyzed 'CO-free' Carbonylation Reaction Uncovered by In-situ Spectroscopy: The Formyl Mechanism
18. Gemischtvalente Verbindungen als polarisierende Mittel für die dynamische Kern‐Overhauser‐Polarisation in Festkörpern**
19. Mixed‐Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids**
20. In Vitro and In Vivo Studies on HPMA-Based Polymeric Micelles Loaded with Curcumin
21. Reaction Mechanism of Pd-catalyzed 'CO-free' Carbonylation Reaction Uncovered by In-situ Spectroscopy: The Formyl Mechanism
22. Mixed-valence compounds as polarizing agents for Overhauser dynamic nuclear polarization in solids
23. Highly Efficient Trityl-nitroxide Biradicals for Biomolecular High-field Dynamic Nuclear Polarization
24. Gemischtvalente Verbindungen als polarisierende Mittel für die dynamische Kern-Overhauser-Polarisation in Festkörpern
25. Gemischtvalente Verbindungen als polarisierende Mittel für die dynamische Kern‑Overhauser‑Polarisation in Festkörpern**
26. Reaction Mechanism of Pd‐Catalyzed “CO‐Free” Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism
27. A site-sensitive quasi-in situ strategy to characterize Mo/HZSM-5 during activation
28. Atomic-level organization of vicinal acid–base pairs through the chemisorption of aniline and derivatives onto mesoporous SBA15† †Electronic supplementary information (ESI) available. See DOI: 10.1039/c6sc01229a
29. From single-site tantalum complexes to nanoparticles of TaxNy and TaOxNy supported on silica: elucidation of synthesis chemistry by dynamic nuclear polarization surface enhanced NMR spectroscopy and X-ray absorption spectroscopy
30. From single-site tantalum complexes to nanoparticles of Ta x N y and TaO x N y supported on silica: elucidation of synthesis chemistry by dynamic nuclear polarization surface enhanced NMR spectroscopy and X-ray absorption spectroscopy
31. Imine Metathesis Catalyzed by a Silica-Supported Hafnium Imido Complex
32. Exploiting the interactions between the ruthenium Hoveyda–Grubbs catalyst and Al-modified mesoporous silica: the case of SBA15vs.KCC-1
33. Predicting the DNP-SENS efficiency in reactive heterogeneous catalysts from hydrophilicity
34. NMR Study of Solvation Effect on the Geometry of Proton-Bound Homodimers of Increasing Size
35. In Vitroand In VivoStudies on HPMA-Based Polymeric Micelles Loaded with Curcumin
36. Enzymatically Degradable Hybrid Organic-Inorganic Bridged Silsesquioxane Nanoparticles for Biomedical Application
37. Solvent-Free Synthesis of Quaternary Metal Sulfide Nanoparticles Derived from Thiourea
38. The structure and binding mode of citrate in the stabilization of gold nanoparticles
39. Reactive surface organometallic complexes observed using dynamic nuclear polarization surface enhanced NMR spectroscopy
40. From single-site tantalum complexes to nanoparticles of TaxNy and TaOxNy supported on silica: elucidation of synthesis chemistry by dynamic nuclear polarization surface enhanced NMR spectroscopy and X-ray absorption spectroscopy
41. NMR Study of Solvation Effect on the Geometry of Proton-Bound Homodimers of Increasing Size
42. Exploiting the interactions between the ruthenium Hoveyda–Grubbs catalyst and Al-modified mesoporous silica: the case of SBA15 vs. KCC-1.
43. Solvent‐Free Synthesis of Quaternary Metal Sulfide Nanoparticles Derived from Thiourea.
44. From single-site tantalum complexes to nanoparticles of TaxNy and TaOxNy supported on silica: elucidation of synthesis chemistry by dynamic nuclear polarization surface enhanced NMR spectroscopy and X-ray absorption spectroscopy
45. Highly Efficient Trityl-Nitroxide Biradicals for Biomolecular High-Field Dynamic Nuclear Polarization.
46. Mixed-Valence Compounds as Polarizing Agents for Overhauser Dynamic Nuclear Polarization in Solids*.
47. In Vitro and In Vivo Studies on HPMA-Based Polymeric Micelles Loaded with Curcumin.
48. Reaction Mechanism of Pd-Catalyzed "CO-Free" Carbonylation Reaction Uncovered by In Situ Spectroscopy: The Formyl Mechanism.
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