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 Київський національний університет
імені Тараса Шевченка

Кафедра аналітичної хімії

2016

Наукові статті співробітників кафедри в журналах, що мають IF

  1. Zaporozhets O. A, Paustovska A. S., Zinko L. S., Davydov V. I. A Simple and Sensitive Fluorescense Method for Fluoride Determination in Dietary Supplements, Fluorinated Salts, and Tea // Food Analytical Methods, 2016, V. 9, No. 11, P. 3193–3200. IF: 2.167 SNIP: 0,83 http://link.springer.com/article/10.1007/s12161-016-0517-3

  2. Mykhailiuk P. K. Synthesis of Fluoroalkyl Pyrazoles from In-Situ-Generated C2F5CHN2 and Electron-Deficient Alkenes // European Journal of Organic Chemistry, 2016, V. 33, Issue 11, P. 5485–5493. IF: 3.068 SNIP: 0,735 http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201600947/full

  3. Gerda V. I. Atomic concentration of hydrogen in tetra- and hexaamine heteroligand chromium(III) complexes with cyclic tetraamines Russian Journal of Applied Chemistry, 2016, V, 89, No. 3, P. 462–466. IF: 0,307 SNIP: 0,460 http://link.springer.com/article/10.1134/S1070427216030186

  4. Sholokh, M., Improta R. Mori M., Sharma R., Kenfack C., Shin D., Voltz, K., Stote, R.H., Zaporozhets O.A., Botta, M., Tor, Y. , Mély, Y. Tautomers of a Fluorescent G Surrogate and Their Distinct Photophysics Provide Additional Information Channels // Angewandte Chemie - International Edition, 2016, V. 55, No. 28, P. 7974–7978. IF: 13.734 SNIP: 2,178 2016. http://onlinelibrary.wiley.com/doi/10.1002/anie.201601688/abstract

  5. Arkhipov A. V., Arkhipov V. V., Cossy J., Kovtunenko V. O., Mykhailiuk P. K. Unexpected Reactivity of Trifluoromethyl Diazomethane (CF3CHN2): Electrophilicity of the Terminal N-Atom // Organic Letters, 2016, V. 18, No. 14, P. 3406–3409. IF: 6,732 SNIP: 1,301. http://pubs.acs.org/doi/abs/10.1021/acs.orglett.6b01565

  6. Levchenko K., Datsenko O. P., Serhiichuk O., Tolmachev A., Iaroshenko V. O., Mykhailiuk P. K. Copper-Catalyzed O-Difluoromethylation of Functionalized Aliphatic Alcohols: Access to Complex Organic Molecules with an OCF2H Group // The Journal of Organic Chemistry, 2016, V. 81, Issue 14, P. 5803–5813. IF: 4.785 SNIP: 1.139. http://pubs.acs.org/doi/abs/10.1021/acs.joc.6b00628

  7. Diyuk V. E., Mariychuk R. T., Lisnyak V. V. Functionalization of activated carbon surface with sulfonated styrene as a facile route for solid acids preparation // Materials Chemistry and Physics, 2016, V. 184, P. 138–145. IF: 2,101 SNIP: 0,970. http://www.sciencedirect.com/science/article/pii/S0254058416306976

  8. Uklein A. V. , Diyuk V. E. , Grishchenko L. M., Kozhanov V. O., Boldyrieva O. Yu., Lisnyak V. V., Multian V. V., Gayvoronsky V. Ya. Characterization of oxidized carbon materials with photoinduced absorption response // Applied Physics B, 2016, V. 122, P. 287–290. IF: 1,856 SNIP: 1.035. http://link.springer.com/article/10.1007/s00340-016-6561-2

  9. Diyuk V. E., Mariychuk R. T., Lisnyak V. V. Barothermal preparation and characterization of micro-mesoporous activated carbons: Textural studies, thermal destruction and evolved gas analysis with TG-TPD-IR technique // Journal of Thermal Analysis and Calorimetry, 2016, V. 124, Issue 2, P. 1119–1130. IF: 2.042 SNIP: 0.951. http://link.springer.com/article/10.1007/s10973-015-5208-6

  10. Tolmachev A., Bogolubsky A. V., Pipko S. E., Grishchenko A. V., Ushakov D. V., Zhemera A. V., Viniychuk O. O., Konovets A. I., Zaporozhets O. A., Mykhailiuk P. K., Moros Yu. S. Expanding Synthesizable Space of Disubstituted 1,2,4-Oxadiazoles // ACS Combinatorial Science, 2016, V. 18, No. 10, P. 616–624. IF: 3,317 SNIP: 0,943. http://pubs.acs.org/doi/abs/10.1021/acscombsci.6b00103

  11. Chalyk B. A., Kandaurova I. Y., Hrebeniuk K. V, Manoilenko O. V., Kulik I. B., Iminov R. T., Kubyshkin V., Tverdokhlebov A. V., Ablialimov O. K., Mykhailiuk P. K. A base promoted multigram synthesis of aminoisoxazoles: valuable building blocks for drug discovery and peptidomimeticsac // RSC Advances, 2016, V. 6, P. 25713–25723. IF: 3,317 SNIP: 0,943. http://pubs.rsc.org/en/Content/ArticleLanding/2016/RA/C6RA02365G#!divAbstract

  12. Alekseev S. A., Коrytko D. М. (аспірант), Grin S. V., Yablokov V. Ye., Khaynakova O. А., Zaitsev V. N. Mesoporous silicon carbide via nanocasting of Ludox xerogel / Kruse Norbert // RSC Advances, 2016, V. 108, P. 108149–108160. IF: 3,289 SNIP: 0,812. http://pubs.rsc.org/en/content/articlelanding/2016/ra/c6ra21972a#!divAbstract

  13. Bogolubsky A. V., Moroz Y. S., Mykhailiuk P. K., Pipko S. E., Grishchenko V., Zhemera A. V., Konovets A. I., Doroschuk R. A., Dmytriv Y. V., Zaporozhets O. A., Tolmachev A. 2,2,2-Trifluoroethyl Oxalates in the One-Pot Parallel Synthesis of Hindered Aliphatic Oxamides // European Journal of Organic Chemistry, 2016, Issue 12, P. 2129–2130. IF: 3.068 SNIP: 0,735. http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201501579/full

  14. Kuchera O. V., Kolodyazhnaya A. O., Smolii O. B., Nazarenko N. K., Kubyshkin V., Mykhailiuk P. K., Tolmachev A. A. Lipase kinetic enantiomeric resolution of 1-heteroarylethanols // Tetrahedron: Asymmetry, 2016, V. 27, Issues 7–8, P. 341–345. IF: 2.155 SNIP: 0,682. http://www.sciencedirect.com/science/article/pii/S0957416616001038

  15. Zaitseva N., Alekseev S., Zaitsev V., Raks V. Solid-Phase Spectrophotometric Analysis of 1-Naphthol Using Silica Functionalized with m-Diazophenylarsonic Acid // Nanoscale Research Letters, V. 11, No 1, Р. 149–156. IF: 2.789 SNIP: 0.611. https://nanoscalereslett.springeropen.com/articles/10.1186/s11671-016-1356-2

  16. Doroschuk V O., Grogul A. B., Mandzyuk Ye. S., Makukha O. G. (аспірант), Grytsyk N. O. Cloud point extraction of disulfiram for its HPLC-MS/MS determination in synthetic urine // Chemical Papers, 2016, V. 70, No 10, P. 1316–1321. IF: 1.326 | SNIP: 0.560. https://www.degruyter.com/view/j/chempap.2016.70.issue-10/chempap-2016-0074/chempap-2016-0074.xml

  17. Uklein А. V., Diyuk V. E., Grishchenko L. M., Kozhanov V. O., Lisnyak V. V., Budnyk P. I., Multian V. V., Gayvoronsky V.Ya. The correlation of photoinduced total transmission with the degree of the surface functionalization of carbons obtained from natural renewable sources // Ukrainian Journal of Physics, 2016, V. 61, Issue 10, P. 863–871. IF: 0.367 SNIP: 0.424. http://ujphys.bitp.kiev.ua/files/journals/61/10/611002p.pdf

  18. Zamotaev O. M., Pivovarenko V. G., Mély Y., Yushchenko D., Shvadcschak V., Sysch Т. P., Mеlnyschuk N. А. Environment-sensitive quinolone demonstrating long-lived fluorescence and unusually slow excited-state intramolecular proton transfer kinetics // Methods and Applications in Fluorescence, 2016, V. 4, Issue 3, P. 034004. IF: 2.429 , SNIP: 1.604. http://iopscience.iop.org/article/10.1088/2050-6120/4/3/034004/meta

  19. Chubar Natalia, Gerda Vasyl, Banerjee Dipanjan, Yablokova Ganna. Effect of Fe(II)/Ce(III) dosage ratio on the structure and anion adsorptive removal of hydrothermally precipitated composites: Insights from EXAFS/XANES, XRD and FTIR // Journal of Colloid and Interface Science, 2017, V.487, P. 388–400. http://www.sciencedirect.com/science/article/pii/S002197971630827X#MMCvFirst

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Taras Shevchenko National University Analytical chemistry department Analytical chemistry scientific council

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