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N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry
Siberian Branch of Russian Academy of Science

Department of physical organic chemistry


Head of Center -
Cand. Sci. (Phys.-Math.) Dmitriy N. Polovyanenko
tel.  (383) 330-96-61
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

Scientific Director
Cand. Sci. (Chem) Victor I. Mamtyuk
tel.  (383) 330-69-60
e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.


The Center of spectral investigations (CSI) has been established on March 11, 2016 on the basis of the Laboratory of Physical Research Methods/
The Centre includes 6 groups.


  • collective use of unique expensive scientific equipment to carry out fundamental and applied research;
  • raising the level of experimental work in the field of molecular spectroscopy, structural and analytical research;
  • assistance in the implementation of scientific and scientific-applied grants and projects;
  • rendering services to organizations and enterprises of the Siberian region;
  • education and training of personnel for measurements, operation and maintenance of scientific instruments.




  • Analysis and identification of methods of molecular spectroscopy of organic, metal organic and inorganic substances and materials, including nanomaterials with desired properties (plastics, optical, ferromagnetic, biologically active) for science, technology and medicine
  • The study of natural and biological methods of molecular spectroscopy, chromatography, and microanalysis
  • Analysis and identification of substances and materials of synthetic, natural and anthropogenic origin, including nanomaterials
  • Development of physical and chemical methods of analysis of substances and materials
  • Creating databases of molecular spectroscopy data
  • independent expertise

Logistical and methodical base of Spectral Research Center allow us to study the liquid, solid and gaseous substances and carry out sample preparation of complex objects of natural, synthetic and natural origin.

The Centre includes 6 groups:

1. Group of Nuclear Magnetic Resonance (GNMR)

Employee Position Room Phone Phone in. email Publications
by years
1 Salnikov Георгий Efimovich Senior Researcher 127 330-55-04 3-25 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Korchagina Dina Vladimirovna Senior Researcher (Cand. Chem.) 412 НТК 330-55-04 2-58 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Skorova Anna Борисовна Leading Engineer 108 330-55-04 3-32 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Kandaurova Vera Vasilievna technicist 106 330-55-04 3-50 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Ardashova Darya Vladimirovna technicist 108 330-55-04 3-32

2. Group of mass spectrometry (GMS)

Employee Position Room Phone Phone in. email Publications
by years
1 Nefedov Andrey Alekseevich Senior Researcher (Cand. Chem.). Group's Head 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Salnikova Olga Иосифовна Leading Engineer 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Statsenko Olga Борисовна Leading Engineer 110 330-78-64 3-31 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Bondareva Mariya Alexandrovna engineer

3. Group of Optical Spectrometry (GOS)

Employee Position Room Phone Phone in. email Publications
by years
1 Karpova Elena Viktorovna Senior Researcher (Cand. Chem.). Group's Head 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Chuikov Igor Petrovich Researcher (Cand. Chem.) 414 НТК 330-82-51 2-15 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Sagalaeva Natalia Ivanovna Senior Laboratory Assistant 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Kornakova Tatyana Aleksandrovna Leading Engineer 104 330-78-64 3-35 This email address is being protected from spambots. You need JavaScript enabled to view it.

4. Group of X-ray analysis (GXRA)

Employee Position Room Phone Phone in. email Publications
by years
1 Bagryanskaya Irina Yurievna Leading Researcher (Doct.Chem), Group's Head 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Gatilov Yurii Vasilievich Leading Researcher (Doct. Chem) 207 НТК 330-78-64 4-37 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Rybalova Tatyana Valerievna Researcher 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.

5. Group of thermal analysis (GTA)

Employee Position Room Phone Phone in. email Publications
by years
1 Shundrina Inna Kazimirovna Senior Researcher (Cand. Chem.). Group's Head 105 330-78-64 3-46 This email address is being protected from spambots. You need JavaScript enabled to view it.



Laboratory staff publications (DB NIOCh)

Reviews, Articles

  1. Yu. Zhuravleva, E.V. Karpova, L.A. Oparina, O.V. Poveschenko, M.A. Surovtseva, A.T. Titov, A.L. Ksenofontov, M.B. Vasilieva, E.V. Kuznetsova, A.V. Bogachev-Prokophiev, B.A. Trofimov
    Cross-linking method using pentaepoxide for improving bovine and porcine bioprosthetic pericardia: a multiparametric assessment study
    Materials Science and Engineering: C, 2021, V. 118, Art. num 111473 doi:10.1016/j.msec.2020.111473, IF=5.88

  1. A.Yu. Makarov, Yu.M. Volkova, L.A. Shundrin, A.A. Dmitriev, I.G. Irtegova, I.Yu. Bagryanskaya, I.K. Shundrina, N.P. Gritsan, J. Beckmann, A.V. Zibarev
    Chemistry of Herz radicals: a new way to near-IR dyes with multiple long-lived and differently-coloured redox states
    Chem. Commun., 2020, 2020,56(5), 727-730 doi:10.1039/C9CC08557B, IF=5.996
  2. E.V. Tretyakov, S.I. Zhivetyeva, P.V. Petunin, D.E. Gorbunov, N.P. Gritsan, I.Yu. Bagryanskaya, A.S. Bogomyakov, P.S. Postnikov, M.S. Kazantsev, M.E. Trusova, I.K. Shundrina, E.V. Zaytseva, D.A. Parkhomenko, E.G. Bagryanskaya, V. Ovcharenko
    Ferromagnetically Coupled S = 1 Chains in Crystals of Verdazyl‐Nitronyl Nitroxide Diradicals
    Angewandte Chemie International Edition, First published: 27 July 2020 doi:10.1002/anie.202010041, IF=12.959
  3. V.V. Krisyuk, S. Urkasymkyzy, T.V. Rybalova, I.V. Korolkov, S.V. Sysoev, T.P. Koretskaya, B.M. Kuchumov, A.E. Turgambaeva
    Volatile trinuclear heterometallic beta-diketonates: structure and thermal properties related to the chemical vapor deposition of composite thin films
    Polyhedron, V. 191, 15 November 2020, 114806 doi:10.1016/j.poly.2020.114806, IF=2.342
  4. L. Politanskaya, I. Bagryanskaya, E. Tretyakov, Ch. Xic
    Highly efficient synthesis of novel fluorinated 3-amino-2-mercaptobenzothiazole-2(3H)-thione derivatives
    Journal of Fluorine Chemistry, 2020, V.239, 109628 doi:10.1016/j.jfluchem.2020.109628, IF=2.322
  5. B.M. Urbagarova, E.E. Shults, V.V. Taraskin, L.D. Radnaeva, T.N. Petrova, T.V. Rybalova, T.S. Frolova, A.G. Pokrovskii, Ja. Ganbaatar
    Chromones and coumarins from Saposhnikovia divaricata (Turcz.) Schischk. Growing in Buryatia and Mongolia and their cytotoxicity
    Journal of Ethnopharmacology, 2020, V. 261, 1125170 doi:10.1016/j.jep.2019.112517, IF=3.69
  6. E. V. Suslov, E. S. Mozhaytsev, D. V. Korchagina, N.I. Bormotov, O. I. Yarovaya, K. P. Volcho, O. A. Serova,A. P. Agafonov, R. A. Maksyutov, L.N. Shishkinab, N F. Salakhutdinov
    New chemical agents based on adamantane–monoterpene conjugates against orthopoxvirus infections
    RSC Medicinal Chemistry, 2020, V. 11, N. 10, Pp 1185-1195 doi:10.1039/D0MD00108B
  7. Т.В. Баулина, И.Ю. Кудрявцев, А.В. Артемьев, И.Ю. Багрянская, М.П. Пасечник, В.К. Брель
    Синтез, молекулярная и кристаллическая структура трис[2-(карбамоилметокси)фенил]- фосфиноксида
    Журнал общей химии. 2020. Т. 90. № 10. С. 1506-1511. doi:10.31857/S0044460X20100054, IF=0.716
  8. A. D. Kuimov,Ch.S.Becker,I.P.Koskin, D. E.Zhaguparov,A.A.Sonina,I.K.Shundrina,P.S.Sherin,M. S.Kazantsev
    2-((9H-fluoren-9-ylidene)methyl)pyridine as a new functional block for aggregation induced emissive and stimuli-responsive materials
    Dyes and Pigments, 2020, V. 181, 108595 doi:10.1016/j.dyepig.2020.108595, IF=4.613
  9. M.P. Davydova, I.Yu. Bagryanskaya, I.A. Bauer, M.I. Rakhmanova, V.P. Morgalyuk, V.K. Brel, A.V. Artem'ev
    Green- and red-phosphorescent Mn(II) iodide complexes derived from 1,3-bis(diphenylphosphinyl)propane
    Polyhedron, 2020, V. 188, 114706 doi:10.1016/j.poly.2020.114706, IF=2.343
  10. Yu.S. Demidova, E.S. Mozhaitsev, E.V. Suslov, A.A. Nefedov, A.A. Saraeva, K.P. Volcho, N.F. Salakhutdinov, A. Simakov, I.L. Simakova, D.Yu. Murzin
    Menthylamine synthesis via gold-catalyzed hydrogenation of menthone oxime
    Applied Catalysis A: General, 2020, V. 605, 117799 doi:10.1016/j.apcata.2020.117799, IF=5.6
  11. V. Romanov, E. Tretyakov, G. Selivanova, J. Li, I. Bagryanskaya, A. Makarov, D. Luneau
    Synthesis and Structure of Fluorinated (Benzo[d]imidazol-2-yl)methanols: Bench Compounds for Diverse Applications
    Crystals 2020, 10(9), 786 doi:10.3390/cryst10090786, IF=2.404
  12. I.V. Oleynik, I.K. Shundrina, I.I. Oleyinik
    Highly active titanium(IV ) dichloride FI catalysts bearing a diallylamino group for the synthesis of disentangled UHMWPE
    Polymers for Advanced Technologies, 2020, V. 31, N 9, Pp 1921-1934 doi:10.1002/pat.4917, IF=2.578
  13. M.Yu. Petyuk, A.S. Berezin, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A dinuclear Re(I) tricarbonyl complex showing thermochromic luminescence
    Inorganic Chemistry Communications, 2020, V.119, 108058 doi:10.1016/j.inoche.2020.108058, IF=1.943
  14. E.A. Chulanova, E.A. Radiush, I.K. Shundrina, I.Yu. Bagryanskaya, N.A. Semenov, J. Beckmann, N.P. Gritsan, A.V. Zibarev
    Lewis Ambiphilicity of 1,2,5-Chalcogenadiazoles for Crystal Engineering: Complexes with Crown Ethers
    Crystal Growth & Design, 2020, V. 20, N 9, Pp 5868-5879 doi:10.1021/acs.cgd.0c00536, IF=4.089
  15. S. M. Adekenov, A. S. Kishkentayeva, M. M. Zhakanov, I. Y. Bagryanskaya
    3-Methoxy-4,5-Methylenedioxypropiophenone and Ferocinin from Ferula kelleri
    Chemistry of Natural Compounds, 2020, V. 56, N 10, Pp 896-898 doi:10.1007/s10600-020-03178-w, IF=0.652
  16. L. Gurskaya, T. Rybalova, I. Beregovaya, E. Zaytseva, M. Kazantsev, E. Tretyakov
    Aromatic nucleophilic substitution: a case study of the interaction of a lithiated nitronyl nitroxide with polyfluorinated quinoline-N-oxides
    Journal of Fluorine Chemistry, 2020, V. 237, 109613 doi:10.1016/j.jfluchem.2020.109613, IF=2.322
  17. I. Zayakin, I. Bagryanskaya, D. Stass, M. Kazantsev, E. Tretyakov
    Synthesis and Structure of (Nitronyl Nitroxide-2-ido)(tert-butyldiphenylphosphine)gold(I) and -(Di(tert-butyl)phenylphosphine)gold(I) Derivatives; Their Comparative Study in the Cross-Coupling Reaction
    Crystals 2020, 10(9), 770 doi:10.3390/cryst10090770, IF=2.404
  18. D.P. Lubov, O.Yu. Lyakin, D.G. Samsonenko, T.V. Rybalova, E.P. Talsi, K.P. Bryliakov
    Palladium aminopyridine complexes catalyzed selective benzylic C–H oxidations with peracetic acid
    Dalton Trans., 2020, V.49, N 32, Pp 11150-11156 doi:10.1039/D0DT02247K, IF=4.174
  19. A.V. Shpatov, T.S. Frolova, S.A. Popov, O.I. Sinitsyna, O.I. Salnikova, G. Zheng, L. Yan, N.V. Sinelnikova, L.M. Pshennikova, A.V. Kochetov
    Lipophilic Metabolites from Five-needle Pines, Pinus armandii and Pinus kwangtungensis, Exhibiting Antibacterial Activity.
    Chemistry & Biodiversity, 2020, V.17, N 8, e2000201 doi:10.1002/cbdv.202000201, IF=2.039
  20. Деревянко Д.И., Басистый В.С., Шелковников В.В., Шундрина И.К., Бухтоярова А.Д., Сальников Г.Е., Бережная В.Н., Черноносов А.А.
    Гибридный фотополимерный материал на основе (8-акрилоил-1,4-дитиа-8-азаспиро[4.5]декан-2-ил)метил акрилата и тиол-силоксанового компонента для записи микроструктур: синтез, оптические и термомеханические свойства
    Высокомолекулярные соединения. Серия Б. 2020. Т. 62. № 5. С. 382-394. doi:10.31857/S2308113920050046, IF=0.976
  21. Reactions of 1-nitro-3,3,3-tribromomethyland 1-nitro-1,3,3,3-tetrabromomethylpropenes with aliphatic dienes/ N. A. Anisimova, E. K. Slobodchikova, M. E. Ivanova, T. V. Rybalova// Russian Journal of General Chemistry, 2020, V. 90, N 8, Pp1388-1397 doi:10.1134/S1070363220080022, IF=0.716
  22. 2-diethylaminovinyl derivatives of halogenated 1,4-quinones: synthetic and structural aspects/ S. I. Zhivetyeva, I. A. Zayakin, I. Yu. Bagryanskaya & E. V. Tretyakov// Journal of Structural Chemistryб 2020, V. 61, N 8, Pp 1253-1259 doi:10.1134/S0022476620080107 , IF=0.745
  23. T.A. Vaganova, Yu.V. Gatilov, D.P. Pishchur, E.V. Malykhin
    Polyfluorinated hydroxy and carboxy benzenes as a new type of H-donors for self-assembly with 18-crown-6 ether: synthesis, supramolecular structure and stability of co-crystals
    Journal of Fluorine Chemistry, 2020, V. 236, 109577 doi:10.1016/j.jfluchem.2020.109577, IF=2.332
  24. I.V. Il'ina, N.S. Dyrkheeva, A.L. Zakharenko, A.Yu. Sidorenko, N.S. Li-Zhulanov, D.V. Korchagina, R. Chand, D.M. Ayine-Tora, A.A. Chepanova, O.D. Zakharova, E.S. Ilina, J. Reynisson, A.A. Malakhova, S.P. Medvedev, S.M. Zakian, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    Design, Synthesis, and Biological Investigation of Novel Classes of 3-Carene-Derived Potent Inhibitors of TDP1
    Molecules 2020, 25(15), 3496 doi:10.3390/molecules25153496, IF=3.267
  25. K.S. Marenin, A.M. Agafontsev, Yu.A. Bryleva, Yu.V. Gatilov, L.A. Glinskaya, D.A. Piryazev, A.V. Tkachev
    Stereochemistry of the Kabachnik-Fields Condensation of Terpenic Amino Oximes with Aldehydes and Dimethyl Phosphite
    ChemistrySelect, 2020, V.5 N 25, Pp 7596-7604 doi:10.1002/slct.202002369, IF=1.811
  26. A.E. Paromov, S.V. Sysolyatin, I.А. Shchurova, A.I. Rogova, V.V. Malykhin, Yu.V. Gatilov
    Synthesis of oxaazaisowurtzitanes by condensation of 4-dimethylaminobenzenesulfonamide with glyoxal
    Tetrahedron, 2020, V. 76, N 27, 131298 doi:10.1016/j.tet.2020.131298, IF=2.233
  27. I. Y. Zhuravleva, Yu.F. Polienko, E. V. Karpova, T. P. Timchenko, M. B. Vasilieva, L. A. Baratova, S. S. Shatskaya, E.V. Kuznetsova, N. R. Nichay, N.Beshchasna, A. V. Bogachev-Prokophiev
    Treatment With Bisphosphonates To Mitigate Calcification Of Elastin-Containing Bioprosthetic Materials
    Journal of Biomedical Materials Research Part A, 2020; V. 108, N 7, Pp 1579-1588 doi:10.1002/jbm.a.36927, IF=3.525
  28. A.Yu. Sidorenko, A.V. Kravtsova, P. Maki-Arvela, A. Aho, T. Sandberg, I.V. Il'ina, N.S. Li-Zhulanov, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, D.Yu. Murzin, V.E. Agabekov
    Synthesis of isobenzofuran derivatives from renewable 2-carene over halloysite nanotubes
    Molecular Catalysis, 2020, V. 490, 110974 doi:10.1016/j.mcat.2020.110974, IF=3.687
  29. Synthesis of Urethane-Type Polymers with Polydimethylsiloxane Blocks for the Manufacture of Fibrous Matrices by Electrospinning/ I. K. Shundrina, I. V. Oleinik, V. I. Pastukhov, L. A. Shundrin, V. S. Chernonosova & P. P. Laktionov// Polymer Science, Series B, 2020, V. 62, N 4, Pp 385-393 doi:10.1134/S1560090420040090, IF=0.976
  30. Effect of the Means Used to Synthesize Highly Fluorinated Polyimide on the Properties of an Adsorbent Prepared on Its Basis/ E. Yu. Yakovleva, E. E. Baranovskaya, I. K. Shundrina & E. Yu. Gerasimov// Russian Journal of Physical Chemistry A, 2020, V. 94, N 7, Pp 1476-1481 doi:10.1134/S0036024420070328, IF=0.719
  31. A.Yu. Makarov, I.Yu. Bagryanskaya, V.V. Zhivonitko
    Interaction of 1,3λ4δ2,2,4-benzodithiadiazines with neutral and charged S-electrophiles: SCl2, C6F5SCl, and NS2+
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp. 968-972 doi:10.1007/s10593-020-02760-y, IF=1.519
  32. N.S. Li-Zhulanov, A.V. Pavlova, D.V. Korchagina, Yu.V. Gatilov, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Synthesis of 1,3-Oxazine Derivatives Based on (-)-Isopulegol using the Ritter Reaction and Study of their Analgesic Activity
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 936-941 doi:10.1007/s10593-020-02753-x, IF=1.519
  33. A. M. Genaev, G. E. Salnikov, K.Yu. Koltunov
    Influence of Positive Charge on the NMR Parameters of Mono- and Diprotonated Forms of 4-Dimethylaminopyridine
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 892-897 doi:10.1007/s10593-020-02749-7, IF=1.519
  34. I.V. Il'ina, O.S. Patrusheva, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    Synthesis of Fluorinated Octahydro-2H-Chromenes in the Presence of the BF3˙Et2O-H2O Catalytic System
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 7, Pp 867-874 doi:10.1007/s10593-020-02743-z, IF=1.519
  35. A new Сu(i) iodide complex showing deep-red luminescence/ A.V. Artemev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya// Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071Journal of Structural Chemistry, 2020, V. 61, N 7, Pp 1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  36. A.V. Artem'ev, M.I. Rakhmanova, K.A. Brylev, I.Yu. Bagryanskaya
    Journal of Structural Chemistry, 2020, V. 61, N 7, pages1068-1071 doi:10.1134/S0022476620070082, IF=0.745
  37. Synthesis of polyfluorinated tetraoxacalix[4]arenes by the interaction of pentafluoronitrobenzene with resorcinol, orcinol, and tetrafluororesorcinol/ Kovtonyuk V. N., Han H., Gatilov Yu. V.// Russian Journal of Organic Chemistry, 2020 doi:10.31857/S0514749220070058, IF=0.751
  38. A.V. Artem'ev, A.S. Berezin, I.V. Taidakov, I.Yu. Bagryanskaya
    Synthesis of dual emitting iodocuprates: can solvents switch the reaction outcome?
    Inorg. Chem. Front., 2020, V. 7, N 11, Pp 2195-2203 doi:10.1039/D0QI00346H, IF=5.958
  39. A 1d coordination polymer based on cui and 2-(diphenylphosphino)pyrimidine: synthesis, structure and luminescent properties/ Davydova M.P., Rakhmanova M.I., Bagryanskaya I.Yu., Brylev K.A., Artem'ev A.V.// Journal of Structural Chemistry, 2020, V. 61, N 6, Pp 894-898 doi:10.1134/S0022476620060086, IF=0.745
  40. M.I. Rogovoy, M.P. Davydova, I.Yu. Bagryanskaya, A.V. Artem'ev
    Efficient one-pot synthesis of diphenyl(pyrazin-2-yl)phosphine and its AgI, AuI, and PtII, complexes
    Mendeleev Communications, 2020, V. 30, N 3, Pp 305-307 doi:10.1016/j.mencom.2020.05.014, IF=1.694
  41. A.V. Markov, A.V. Sen’kova, O.V. Salomatina, E.B. Logashenko, D.V. Korchagina, N.F. Salakhutdinov, M.A. Zenkova
    Trioxolone Methyl, a Novel Cyano Enone-Bearing 18βH-Glycyrrhetinic Acid Derivative, Ameliorates Dextran Sulphate Sodium-Induced Colitis in Mice
    Molecules 2020, 25(10), 2406 doi:10.3390/molecules25102406, IF=3.267
  42. M. Rogovoy, T. Frolova, D. Samsonenko, A. Berezin, I. Bagryanskaya, N. Nedolya, O. Tarasova, V. Fedin, A.V. Artem'ev
    0D to 3D coordination assemblies engineered on 2-(alkylsulfanyl)azine ligands: crystal structures, dual luminescence and cytotoxic activity
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 17, Pp 1635-1644 doi:10.1002/ejic.202000109, IF=2.529
  43. S. Dobrynin, S. Kutseikin, D. Morozov, O. Krumkacheva, A. Spitsyna, Yu. Gatilov, V. Silnikov, G. Angelovski, M.K. Bowman, I. Kirilyuk, A. Chubarov
    Human Serum Albumin Labelled with Sterically-Hindered Nitroxides as Potential MRI Contrast Agents
    Molecules 2020, 25(7), 1709 doi:10.3390/molecules25071709, IF=3.267
  44. A.A. Gostev, I.K. Shundrina, V.I. Pastukhov, A.V. Shutov, V.S. Chernonosova, A.A. Karpenko, P.P. Laktionov
    In Vivo Stability of Polyurethane-Based Electrospun Vascular Grafts in Terms of Chemistry and Mechanics
    Polymers 2020, 12(4), 845 doi:10.3390/polym12040845, IF=3.426
  45. D.E. Votkina, P.V. Petunin, S.I. Zhivetyeva, I.Yu. Bagryanskaya, M.N. Uvarov, M.S. Kazantsev, M.E. Trusova, E.V. Tretyakov, P.S. Postnikov
    Preparation of Multi-spin Systems: a Case Study of Tolane-bridged Verdazyl-based Hetero-diradicals
    European Journal of Organic Chemistry, 2020, V. 2020, N 13, Pp 1996-2004 doi:10.1002/ejoc.202000044, IF=2.889
  46. V.A. Logvinenko, V.P. Fadeeva, B.A. Selivanov, V.D. Tikhova, A.A. Nefedov, A.Ya. Tikhonov
    Thermal decomposition of several N,N'-bis(2-hydroxyiminoalkyl)-α,α'-dinitrones
    Journal of Thermal Analysis and Calorimetry, 2020, V. 140, N 2, Pp 685-693 doi:10.1007/s10973-019-08868-4, IF=2.731
  47. I. Il'ina, E. Morozova, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of aliphatic ketones-derived chiral hexahydro-2H-chromenes
    Medicinal Chemistry Research, 2020, V. 29, N 4, pp 738-747 doi:10.1007/s00044-020-02518-3, IF=1.783
  48. D.S. Odintsov, I.K. Shundrina, I.A. Os'kina, I.V. Oleynik, J. Beckmann, L.A. Shundrin
    Ambipolar polyimides with pendant groups based on 9H-thioxanthene-9-one derivatives: synthesis, thermostability, electrochemical and electrochromic properties
    Polymer Chemistry, 2020, V. 11, N 12, Pp 2243-2251 doi:10.1039/C9PY01930H, IF=5.342
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    Magnetic Properties of π-Conjugated Hybrid Phenoxyl-Nitroxide Radicals with Extended π-Spin Delocalization
    The Journal of Physical Chemistry A, 2020, 124, 12, 2416-2426 doi:10.1021/acs.jpca.9b11856, IF=2.6
  50. A.A. Sinitsyna, S.G. Il’yasov, M.V. ChikinaIlia, I.V. Eltsov, A.A. Nefedov
    A search for synthetic routes to tetrabenzylglycoluril
    Chemical Papers, 2020, V. 74, N 3, pp 1019-1025 doi:10.1007/s11696-019-00941-4, IF=1.68
  51. Synthesis and analgesic activity of 1,3,5-trisubstituted pyrazoles containing a diterpenoid moiety/ M.E. Mironov, A.I. Poltanovich , T.V., Rybalova, M.P. Dolgikh, T.G. Tolstikova, E.E Shults// Russian Chemical Bulletin, 2020, V. 69, Pp 537–546 doi:10.1007/s11172-020-2795-6, IF=1.061
  52. M. Davydova, I. Bauer, V. Brel, M. Rakhmanova, I. Bagryanskaya, A.V. Artem'ev
    Manganese(II) thiocyanate complexes with bis(phosphine oxide) ligands: synthesis and excitation wavelength-dependent multicolor luminescence
    European Journal of Inorganic Chemistry, 2020, V. 2020, N 8, Pp 695-703 doi:10.1002/ejic.201901213, IF=2.529
  53. I.F. Zhurko, S. Dobrynin, A.A. Gorodetskii, Yu.I. Glazachev, T.V. Rybalova, E.I. Chernyak, N. Asanbaeva, E.G. Bagryanskaya, I.A. Kirilyuk
    2-Butyl-2-tert-butyl-5,5-diethylpyrrolidine-1-oxyls: Synthesis and Properties
    Molecules 2020, 25(4), 845 doi:10.3390/molecules25040845, IF=3.267
  54. A.A. Kotlyarova, K.Yu. Ponomarev, E.A. Morozova, D.V. Korchagina, E.V. Suslov, A.V. Pavlova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    The effect of 3,7-diazabicyclo[3.3.1]nonanes containing monoterpenoid moieties on the physical activity of mice
    Journal of research in pharmacy, 2020, V. 24, N 2, Pp 196-204 doi:10.35333/jrp.2020.136
  55. V.V. Chernyshov, O.I. Yarovaya, D.S. Fadeev, Yu.V. Gatilov, Ya.L. Esaulkova, A.S. Muryleva, K.O. Sinegubova, V.V. Zarubaev, N.F. Salakhutdinov
    Single-stage synthesis of heterocyclic alkaloid-like compounds from (+)-camphoric acid and their antiviral activity
    Molecular Diversity, 2020, V. 24, N 1, Pp 61-67 doi:10.1007/s11030-019-09932-9, IF=2.013
  56. E.B. Nikolaenkova, I.Yu. Bagryanskaya, A.Ya. Tikhonov
    Synthesis of 2-[2-(hydroxyimino)alkyl]-1,2-oxazol-5(2Н)-ones
    Chemistry of Heterocyclic Compounds, 2020, V. 56, N 2, Pp 208-212 doi:10.1007/s10593-020-02645-0, IF=1.519
  57. Synthesis and structure of 9-hydroxy-1,2-dicarba-closo-dodecaborane(11)/ D. A. Rudakov, A. M. Genaev, Yu. V. Gatilov, E. A. Dikusar, T. D. Zvereva, Z. P. Zubreichuk & V. I. Potkin// Russian Chemical Bulten, 2020, V. 69, N 2, Pp 320-324 doi:10.1007/s11172-020-2763-1, IF=1.061
  58. T. M. Khomenko , A. L. Zakharenko , A. A. Chepanova , E. S. Ilina , O. D. Zakharova , V. I. Kaledin , V. P. Nikolin , N. A. Popova , D. V. Korchagina , J. Reynisson , R. Chand , D.l M. Ayine-Tora , J. Patel , I. K. H. Leung , K. P. Volcho , N. F. Salakhutdinov, O. I. Lavrik
    Promising New Inhibitors of Tyrosyl-DNA Phosphodiesterase I (Tdp 1) Combining 4-Arylcoumarin and Monoterpenoid Moieties as Components of Complex Antitumor Therapy
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  59. P.V. Petunin, T.V. Rybalova, M.E. Trusova, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, L. Postulka, P. Eibisch, B. Wolf, M. Lang, P.S. Postnikov, M. Baumgarten
    A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units
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  60. QUALITY AND QUANTITATIVE COMPOSITION OF SUNFLOWER OIL DEODORIZATION DISTILLATE/ Kukina T.P., Shcherbakov D.N., Panteleyeva N. V., Sal'nikova O. I., Kolosov P.V.// doi:10.14258/jcprm.2020015909
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    Synthesis and Analgesic Activity of Monoterpenoid Aldehyde-derived Hydro-2H-chromeneols
    Letters in Drug Design & Discovery, 2020, V. 17, N 1, Pp 68-78 doi:10.2174/1570180816666181114131220, IF=1.169

  1. An unusual fabric from Jety-Asar-2, Eastern Aral sea region, in the context of the central asian textile tradition/ POLOSMAK N.V., KARPOVA E.V., AMOSOV E.V.// doi:10.17746/1563-0102.2020.48.3.050-058
  2. M.S. Kazantsev, A.A. Sonina, I.P. Koskin, P.S. Sherin, T.V. Rybalova, E. Benassi, E.A. Mostovich
    Stimuli responsive aggregation-induced emission of bis(4-((9H-fluoren-9-ylidene)methyl)phenyl)thiophene single crystals
    Mater. Chem. Front., 2019, V. 3, N 8, Pp 1545-1554 doi:10.1039/C9QM00198K
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    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  4. A.Yu.Sidorenko,A.V.Kravtsova,I.V.Il'ina,J.Warna,D.V.Korchagina,Yu.V.Gatilov,K.P.Volcho,N.F.Salakhutdinov,D.Yu.Murzin, V.E.Agabekov
    Clay nanotubes catalyzed solvent-free synthesis of octahydro-2H-chromenols with pharmaceutical potential from (-)-isopulegol and ketones
    Journal of Catalysis, 2019, V. 380, Pp 145-152 doi:10.1016/j.jcat.2019.10.015, IF=7.723
  5. A. Zaikovskii, S. Novopashin, V. Maltsev, T. Kardash, I. Shundrina
    Tin-carbon nanomaterial formation in a helium atmosphere during arc-discharge
    RSC Adv., 2019, V. 9, N 63, Pp 36621-36630 doi:10.1039/C9RA05485E, IF=3.049
  6. G.T. Sukhanov, Yu.V. Filippova, A.G. Sukhanova, I.Yu. Bagryanskaya, K.K. Bosov
    Synthesis of 1-(Adamantan-1-yl)-1H-1,2,3-Triazoles and their Salts by Adamantylation in AdOH–HClO4 and AdOH–H2SO44 Systems
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 12, pp 1197-1203 doi:10.1007/s10593-019-02601-7, IF=1.491
  7. Thermal Reactions of 6-Bromo-, 6-Chloro-, and 6-(Methylsulfanyl)octafluoroindane-5-thioles with Tetrafluorethylene. Synthesis of Dodecafluoro-2H,3H,5H,6H,7H-indeno[5,6-b]thiophene/ P.V. Nikul'shin, A.M. Maksimov, Yu. V. Gatilov, V.E. Platonov// Russian Journal of General Chemistry, 2019, V. 89, N: 12, Pp 2378-2385 doi: 10.1134/S0044460X19120096 doi:10.1134/S1070363219120090, IF=0.643
  8. V.V. Chernyshov, Y.V. Gatilov, O.I. Yarovaya, I.P. Koskin, S.S. Yarovoy, K.A. Brylev, N.F. Salakhutdinov
    The first example of the stereoselective synthesis and crystal structure of a spirobi­cyclo­quinazolinone based on (–)-fenchone and anthranilamide
    Acta Crystallographica Section C, V. C75, Part 12, Pp 1675-1680 doi:10.1107/S2053229619015766, IF=0.93
  9. G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
    Direct electrophilic fluorination of naproxen with NF-reagents
    Journal of Fluorine Chemistry, 2019, V. 228, 109412 doi:10.1016/j.jfluchem.2019.109412, IF=2.055
  10. I. Sokol, A. Sokol, T. Bul'bak, A. Nefyodov, P. Zaikin, A. Tomilenko
    C- and N-bearing Species in Reduced Fluids in the Simplified C-O-H-N System and in Natural Pelite at Upper Mantle P-T Conditions
    Minerals 2019, 9(11), 712 doi:10.3390/min9110712, IF=2.25
  11. S.A. Dobrynin, I.A. Kirilyuk, Yu.V. Gatilov, A.A. Kuzhelev, O.A. Krumkacheva, M.V. Fedin, M.K. Bowman, E.G. Bagryanskaya
    Unexpected one-pot formation of the 1H-6a,8a-epiminotri-cyclopenta[a,c,e][8]annulene system from cyclopentanone, ammonia and dimethyl fumarate. Synthesis of highly strained polycyclic nitroxide and EPR study
    Beilstein Journal of Organic Chemistry, 2019, V. 15, Pp 2664-2670 doi:10.3762/bjoc.15.259, IF=2.595
  12. E.P. Talsi, A.A. Bryliakova, R.V. Ottenbacher, T.V. Rybalova, K.P. Bryliakov
    Chiral Autoamplification Meets Dynamic Chirality Control to Suggest Nonautocatalytic Chemical Model of Prebiotic Chirality Amplification
    Research, 2019, V.2019. Article ID: 4756025 doi:10.34133/2019/4756025
  13. M.E. Mironov, O.S. Oleshko, M.A. Pokrovskii, T.V. Rybalova, V.K. Pechurov, A.G. Pokrovskii, S.V. Cheresis, S.V. Mishinov, V.V. Stupak, E.E. Shults
    6-(4'-Aryl-1',2',3'-triazolyl)-spirostan-3,5-diols and 6-(4'-Aryl-1',2',3'-triazolyl)-7-hydroxyspirosta-1,4-dien-3-ones: Synthesis and analysis of their cytotoxicity
    Steroids, 2019, V. 151, Article's number 108460 doi:10.1016/j.steroids.2019.108460, IF=2.136
  14. A.V. Artem'ev, M.Z. Shafikov, A. Schinabeck, O.V. Antonova, A.S. Berezin, I.Yu. Bagryanskaya, P.E. Plusnin, H. Yersin
    Sky-blue thermally activated delayed fluorescence (TADF) based on Ag(i) complexes: strong solvation-induced emission enhancement
    Inorg. Chem. Front., 2019, V. 6, N 11, Pp 3168-3176 doi:10.1039/C9QI01069F, IF=5.934
  15. A.L. Shatsauskas, E.R. Saibulina, Yu.V. Gatilov, A.S. Kostyuchenko, A.S. Fisyuk
    Synthesis of benzo[c][1,7]naphthyridine derivatives
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 11, pp 1080-1086 doi:10.1007/s10593-019-02581-8, IF=1.492
  16. Effective Inhibitors of Tyrosyl-DNA Phosphodiesterase 1 Based on Monoterpenoids as Potential Agents for Antitumor Therapy/ A.A. Chepanova, N.S. Li-Zhulanov, A.S. Sukhikh, A. Zafar, J. Reynisson, A.L. Zakharenko, O.D. Zakharova, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik// Russian Journal of Bioorganic Chemistry, 2019, Vol. 45, No. 6, pp. 647-655. doi:10.1134/S1068162019060104, IF=0.794
  17. Peculiarities of Interaction of 2-Amino-1,4-naphthoquinones with 2,2-Dihydroxy-1H-inden-1,3(2H)-dione/ L.M. Gornostaev, O.I. Fominykh, T.I. Lavrikova, Yu.G. Khalyavina, Yu.V. Gatilov, G.A.. Stashina// Russian Journal of Organic Chemistry, 2019, Vol. 55, No. 11, pp. 1716-1725 (doi:10.1134/S0514749219110132) doi:10.1134/S1070428019110125, IF=0.751
  18. A.V. Lipeeva, D.O. Zakharov, Yu.V. Gatilov, M.A. Pokrovskii, A.G. Pokrovskii, E.E. Shults
    Design and Synthesis of 3-(N-Substituted)aminocoumarins as Anticancer Agents from 3-Bromopeuruthenicin
    ChemistrySelect, 2019, V. 4, N 34, Pp 10197-10201 doi:10.1002/slct.201901377, IF=1.716
  19. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
    A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
    ACS Chemical Neuroscience, 2019, V. 10, N 10, Pp 4337-4349 doi:10.1021/acschemneuro.9b00396, IF=3.861
  20. A.V. Artem'ev, M.R. Ryzhikov, A.S. Berezin, I.E. Kolesnikov, D.G. Samsonenko, I.Yu. Bagryanskaya
    Photoluminescence of Ag(I) complexes with a square-planar coordination geometry: the first observation
    Inorg. Chem. Front., 2019, V. 6, N 10, Pp 2855-2864 doi:10.1039/C9QI00657E, IF=5.934
  21. N.A. Semenov, E.A. Radiush, E.A. Chulanova, A.M. Z. Slawin, J.D. Woollins, E.M. Kadilenko, I.Yu. Bagryanskaya, I.G. Irtegova, A.S. Bogomyakov, L.A. Shundrin, N.P. Gritsan, A.V. Zibarev
    Design, synthesis and isolation of a new 1,2,5-selenadiazolidyl and structural and magnetic characterization of its alkali-metal salts
    New J. Chem., 2019, V. 43, N 41, Pp 16331-16337 doi:10.1039/C9NJ04069B, IF=3.69
  22. V.A. Savel'ev, A.A. Kotova, T.V. Rybalova, E.E. Shults
    Regioselective Synthesis of 1,3,5-Trisubstituted Pyrazoles Containing an Anthranilic Acid Motif
    Chemistry of Heterocyclic Compounds, 2019, V. 55, N 10, pp 943-955 doi:10.1007/s10593-019-02561-y, IF=1.492
  23. Е.В. Карпова, И.К. Шундрина, Е. Орлова, А. Коновалов
    Ароматические и минеральные вещества в тканях образцов яровой мягкой пшеницы Triticum aestivum L., различающихся по устойчивости к бурой ржавчине (возбудитель Puccinia triticina Erikss.)
    Химия растительного сырья, 2019, 4, стр. 87-95 doi:10.14258/jcprm.2019045238
  24. Study of Plant Coumarins: XVII. Synthesis and Transformations of 6-Carboxamidocoumarins/ E.E.Shults, D.O. Zakharov, A.V. Lipeeva, Yu.V. Gatilov, A.G. Makarov// Russian Journal of Organic Chemistry, 2019, V. 55, N 10, pp 1518-1526 doi:10.1134/S1070428019100099, IF=0.751
  25. A.I. Titkov, O.A. Logutenko, A.M. Vorobyov, E.Yu. Gerasimov, I.K. Shundrina, N.V. Bulina, N.Z. Lyakhov
    Synthesis of ˜10 nm size Cu/Ag core-shell nanoparticles stabilized by an ethoxylated carboxylic acid for conductive ink
    Colloids and Surfaces A: Physicochemical and Engineering Aspects, 2019, V. 577, Pp 500-508 doi:10.1016/j.colsurfa.2019.06.008, IF=3.131
  26. T.A. Vaganova, Yu.V. Gatilov, E. Benassi, I.P. Chuikov, D.P. Pishchur, E.V. Malykhin
    Impact of molecular packing rearrangement on solid-state fluorescence: polyhalogenated N-hetarylamines vs. their co-crystals with 18-crown-6
    CrystEngComm, 2019, V. 21, N 39, Pp 5931-5946 doi:10.1039/C9CE00645A, IF=3.381
  27. E. S. Vasilyev, S. N. Bizyaev, V.Yu. Komarov, Yu.V. Gatilov, A. V. Tkachev
    Chiral C2-Symmetric Diimines with 4,5-Diazafluorene Units
    Molecules 2019, 24(17), 3186 doi:10.3390/molecules24173186, IF=3.59
  28. P.V. Petunin, D.E. Votkina, M.E. Trusova, T.V. Rybalova, E.V. Amosov, M.N. Uvarov, P.S. Postnikov, M.S. Kazantsev, E.A. Mostovich
    Oxidative addition of verdazyl halogenides to Pd(PPh3)4
    New J. Chem., 2019, V.43, N 38, Pp15293-15301 doi:10.1039/C9NJ03361K, IF=3.69
  29. A.S. Berezin, M.P. Davydova, I.Yu. Bagryanskaya, O.I. Artyushin, V.K. Brel, A.V. Artem'ev
    A red-emitting Mn(II)-based coordination polymer build on 1,2,4,5-tetrakis(diphenylphosphinyl)benzene
    Inorganic Chemistry Communications, 2019, V. 107, Article's number 107473 doi:10.1016/j.inoche.2019.107473, IF=1.795
  30. M.A. Gromova, Yu.V. Kharitonov, T.V. Rybalova, E.E. Shul'ts
    Synthetic Transformations of Higher Terpenoids. 38.* Synthesis of Conjugates Containing β-Carboline and Tricyclic Diterpenoids
    Chemistry of Natural Compounds, 2019, V. 55, N 5, pp 871-877 doi:10.1007/s10600-019-02836-y, IF=0.566
  31. Aliphatic and triterpenoic products of ether extracts saponification of POPULUS NIGRA L/ T. P. Kukina, I. A. Elshin , O. I. Salnikova , I. V. Eltsov// doi:10.14258/jcprm.2019034951
  32. G. Audran, E. Bagryanskaya, I. Bagryanskaya, M. Edeleva, J.-P. Joly, S-R.A. Marque, A. Iurchenkova, P. Kaletina, S. Cherkasov, T.To. Hai, E. Tretyakov, S. Zhivetyeva
    How intramolecular coordination bonding (ICB) controls the homolysis of the C-ON bond in alkoxyamines
    RSC Adv., 2019,V. 9, N 44, Pp 25776-25789 doi:10.1039/C9RA05334D, IF=3.049
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    Synthesis of silver nanoparticles stabilized by carboxylated methoxypolyethylene glycols: the role of carboxyl terminal groups in the particle size and morphology
    Journal of Inclusion Phenomena and Macrocyclic Chemistry, 2019, V. 94, N 3-4, pp 287-295, SI doi:10.1007/s10847-019-00921-x, IF=1.429
  34. A.Yu. Baranov, M.I. Rakhmanova, D.G. Samsonenko, S.F. Malysheva, N.A. Belogorlova, I.Yu. Bagryanskaya, V.P. Fedin, A.V. Artem'ev
    Silver(I) and gold(I) complexes with tris[2-(2-pyridyl)ethyl]phosphine
    Inorganica Chimica Acta, 2019, V. 494, Pp 78-83 doi:10.1016/j.ica.2019.05.015, IF=2.433
  35. A.A. Chepanova, E.S. Mozhaitsev, A.A. Munkuev, E.V. Suslov, D.V. Korchagina, O.D. Zakharova, A.L. Zakharenko, J. Patel, D.M. Ayine-Tora, J. Reynisson, I.K. H. Leung, K.P. Volcho, N.F. Salakhutdinov, O.I. Lavrik
    The Development of Tyrosyl-DNA Phosphodiesterase 1 Inhibitors. Combination of Monoterpene and Adamantine Moieties via Amide or Thioamide Bridges
    Applied Sciences, 2019, 9(13), 2767 doi:10.3390/app9132767, IF=2.217
  36. Synthesis, structure and emission properties of [Cu2(μ2-I)2L4] complex based on 2-(methylthio)pyrazine/ A. V. Artem'ev, A. S. Beresin, I. Yu. Bagryanskaya// Journal of Structural Chemistry, 2019, V. 60, N 6, pp 967-971 doi:10.1134/S0022476619060118, IF=0.541
  37. V.N. Kovtonyuk, Yu.V. Gatilov, G.E. Salnikov, E.V. Amosov
    Polyfluorinated tetraoxacalixarenes and bicyclooxacalixarenes. Interaction of pentafluorobenzonitrile with resorcinol, orcinol and tetrafluororesorcinol
    Journal of Fluorine Chemistry, 2019, V. 222-223, Pp 59-67 doi:10.1016/j.jfluchem.2019.04.011, IF=2.055
  38. A.M. Genaev, L.N. Shchegoleva, G.E. Salnikov, A.V. Shernyukov, L.A. Shundrin, I.K. Shundrina, Z. Zhu, K.Yu. Koltunov
    Acid-Catalyzed vs. Thermally Induced C1-C1' Bond Cleavage in 1,1'-Bi-2-naphthol. An Experimental and Theoretical Study
    J. Org. Chem., 2019, V. 84, N 11, Pp 7238-7243 doi:10.1021/acs.joc.9b00915, IF=4.745
  39. T.M. Khomenko, D.V. Korchagina, D.S. Baev, P.M. Vassiliev, K.P. Volcho, N.F. Salakhutdinov
    Antimicrobial Activity of Substituted Benzopentathiepin-6-amines
    Journal of Antibiotics, 2019, V. 72, pp 590-599 doi:10.1038/s41429-019-0191-y, IF=2.446
  40. E. Avdeeva, E. Shults, T. Rybalova, Ya. Reshetov, E. Porokhova, I. Sukhodolo, L. Litvinova, V. Shupletsova, O. Khaziakhmatova, I. Khlusov, A. Guryev, M. Belousov
    Chelidonic Acid and Its Derivatives from Saussurea Controversa: Isolation, Structural Elucidation and Influence on the Osteogenic Differentiation of Multipotent Mesenchymal Stromal Cells In Vitro
    Biomolecules, 2019, 9(5), 189 doi:10.3390/biom9050189, IF=4.694
  41. Z. Zhu, A.M. Genaev, G.E. Salnikov, K.Yu. Koltunov
    Mechanistic investigation of superelectrophilic activation of 1,1'-bi-2-naphthols in the presence of aluminum halides
    Org. Biomol. Chem., 2019, V. 17, N 16, Pp 3971-3977 doi:10.1039/C9OB00640K, IF=3.49
  42. Synthesis and analgesic activity of octahydro-2H-chromenols, derivatives of aliphatic ketones/ I. V. Il'ina, D. V. Korchagina, E. A. Morozova, T. G. Tolstikova, K. P. Volcho, N. F. Salakhutdinov// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1061-1066 doi:10.1007/s11172-019-2520-5, IF=1.014
  43. Synthesis, hypolipidemic and antifungal activity of tetrahydroberberrubine sulfonates/ I. V. Nechepurenko, E. D. Shirokova, M. V. Khvostov, T. S. Frolova, O. I. Sinitsyna, A. M. Maksimov, R. A. Bredikhin, N. I. Komarova, D. S. Fadeev, O. A. Luzina, T. G. Tolstikova, N. F. Salakhutdinova// Russian Chemical Bulletin, 2019, V. 68, N 5, pp 1052-1060 doi:10.1007/s11172-019-2519-y, IF=1.014
  44. Effect of Aliphatic Diols and Dicarboxylic Acids on the Properties of Ethylene Succinate Copolyesters/ A. G. Potapov, I. K. Shundrina// Polymer Science, Series A, 2019, V. 61, N 5, pp 544-554 doi:10.1134/S0965545X19050146, IF=0.984
  45. On the Reaction of 2-Benzylamino-1,4-naphthoquinones with Nitrosylsulfuric Acid/ L. M. Gornostaev, E. V. Nuretdinova, T. I. Lavrikova, Yu. G. Khalyavina, O. I. Fominykh, Yu. V. Gatilov// Russian Journal of Organic Chemistry, 2019, V. 55, N 5, pp 608–614 doi:10.1134/S1070428019050051, IF=0.751
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    Synthesis of delta-Carbolines and the Alkaloid Quindoline through a Molybdenum-Catalyzed Cadogan Cyclization and their Photoluminescent Properties
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    Novel Inhibitors of DNA Repair Enzyme TDP1 Combining Monoterpenoid and Adamantane Fragments
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    Synthesis and Optical Properties of Alkaloid Quindoline, Its Structural Analogues and Substituted δ-Carbolines
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  61. Fabrication of High-Aspect-Ratio Microstructures on Tetraacrylate/Acrylamide Monomers Using Synchrotron Radiation/ D. I. Derevyanko, N. A. Orlova, V. V. Shelkovnikov, I. K. Shundrina, B. G. Goldenberg, V. P. Korolkov// High Energy Chemistry, 2019, V. 53, N 2, pp 136-142 doi:10.1134/S0018143919020048, IF=0.634
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    Synthetic modifications of carboline alkaloid harmine: synthesis of 8-substituted derivatives
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  63. Generation of Perfluoroand 1-Chloroperfluoroindanyl and -Benzocyclobutenyl Cations with Perfluoroalkyl Groups in the Aliphatic Ring/ T.V. Mezhenkova, V.M. Karpov, Ya.V. Zonov , I.P. Chuikov// Russian Journal of Organic Chemistry, 2019, V. 55, N 2, pp 193–201 doi:10.1134/S1070428019020118, IF=0.751
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    Radical Anions of Aromatic Carbonitriles as Reagents for Arylation of Fluorinated Benzonitriles
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    Radical Anions, Radical-Anion Salts and Anionic Complexes of 2,1,3-Benzochalcogenadiazoles (S, Se, Te)
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    Using Minisci Reaction for Modification of the tris-Dioximate Metal Clathrochelates: Free-Radical Substitution at the Glyoximate Fragment of an Iron(II)-Encapsulating Cage Framework
    Macroheterocycles, 2016, 9(4), 413-417 doi:10.6060/mhc161182b, IF=0.804
  16. A.B. Burdukov, R. Sipos, N.V. Pervukhina, N.V. Kuratieva, I.V. Eltsov, M.A. Vershinin, E.G. Boguslavsky, D.B. Kal'nyi,S. L. Selektor, A.V. Shokurov,Ya. Z. Voloshin, A.A. Nefedov
    Synthesis, X-Ray Structure and (Spectro)electrochemical Study of an Electrochromic Iron(II) Chlathrochelate with Tuned Redox Properties
    Macroheterocycles 2016 9(3) 257-262 doi:10.6060/mhc160537b, IF=0.804
  17. A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
    Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
  18. E.P. Talsi, T.V. Rybalova, K.P. Bryliakov
    Ti-Salalen Mediated Asymmetric Epoxidation of Olefins with H2O2: Effect of Ligand on the Catalytic Performance, and Insight into the Oxidation Mechanism
    Journal of Molecular Catalysis A: Chemical, 2016, V. 421, 2016, Pages 131-137 doi:10.1016/j.molcata.2016.05.019, IF=3.957
  19. G.I. Borodkin, I.R. Elanov, Yu.V. Gatilov, V.G. Shubin
    Promotional effect of ionic liquids in electrophilic fluorination of methylated uracils
    RSC Advances, 2016, V. 6, N 6, Pp 60556-60564 doi:10.1039/C6RA10850D, IF=3.289
  20. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
    Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
    Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
  21. Ya.V. Zonov, V.M. Karpov, T.V. Mezhenkova, T.V. Rybalova, Yu.V. Gatilov, V.E. Platonov
    Transformations of perfluorinated 1,2-dialkyl-, 1,1- and 1,2-alkylphenylbenzocyclobutenes to indan-2-one and isochromene derivatives under the action of CO/SbF5
    Journal of Fluorine Chemistry, 2016, V. 188, August 2016, Pp 117-125 doi:10.1016/j.jfluchem.2016.06.014, IF=2.213
  22. A.G. Potapov, I.K. Shundrina
    The influence of different fillers on mechanical and physical properties of high-molecular-weight biodegradable aliphatic polyesters
    Polymer Science Series A, July 2016, V. 58, N 4, pp 585-592 doi:10.1134/S0965545X1604012X, IF=0.759
  23. L.A. Oparina, A.V. Artem'ev, O.V. Vysotskaya, O.A. Tarasova, V.A. Shagun, I.Yu. Bagryanskaya, B.A. Trofimov
    Unexpected acid-catalyzed ferrocenylmethylation of diverse nucleophiles with vinyloxymethylferrocene
    Tetrahedron, 2016, V. 72, N 29, Pp 4414-4422 doi:10.1016/j.tet.2016.06.012, IF=2.644
  24. O.P. Korobeinichev, M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, Y. Hu
    Counterflow flames of ultrahigh-molecular-weight polyethylene with and without triphenylphosphate
    Combustion and Flame, 2016, V. 169, July 2016, Pp 261-271 doi:10.1016/j.combustflame.2016.04.019, IF=4.168
  25. A.M. Sheveleva, M.Yu. Ivanov, I.K. Shundrina, A.D. Bukhtoyarova, E.G. Bagryanskaya, M.V. Fedin
    Continuous Wave and Time-Resolved Electron Paramagnetic Resonance Study of Photoinduced Radicals in Fluoroacrylic Porous Polymer Films
    J. Phys. Chem. C, 2016, 120 (27), Pp 14767-14773 doi:10.1021/acs.jpcc.6b05016, IF=4.508
  26. E. Nazimova, A. Pavlova, O. Mikhalchenko, I. Il'ina, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Discovery of highly potent analgesic activity of isopulegol-derived (2R,4aR,7R,8aR)-4,7-dimethyl-2-(thiophen-2-yl)octahydro-2H-chromen-4-ol
    Medicinal Chemistry Research, 2016, V. 25, N 7, pp 1369-1383 doi:10.1007/s00044-016-1573-3, IF=1.435
  27. Synthesis of polyfluorinated A3B tetraoxacalix[4]arenes/ V.N. Kovtonyuk, Yu.V. Gatilov// Russian Journal of Organic Chemistry, 2016, V. 52, N 7, pp 946-949 doi:10.1134/S1070428016070046, IF=0.759
  28. A.V. Artem'ev, N.K. Gusarova, A.O. Sutyrina, Y.V. Gatilov, B.A. Trofimov
    Synthesis of tris[2-(2-furyl)ethyl]phosphine its chalcogenides and PdII complex
    Mendeleev Communications, 2016, V. 26, N 4, Pp 314-316 doi:10.1016/j.mencom.2016.07.016, IF=1.404
  29. D.S. Baranov, Y.V. Gatilov
    Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines
    Mendeleev Communications, 2016, V. 26, N 4, Pp 282-284 doi:10.1016/j.mencom.2016.07.004, IF=1.404
  30. A.V. Artem'ev, N.K. Gusarova, I.Yu. Bagryanskaya, Yu.V. Gatilov, A.O. Sutyrina
    First heteroleptic diselenophosphinate and thioselenophosphinate nickel(II) complexes with N-donor co-ligands
    Polyhedron, V. 111, 17 June 2016, Pp 79-85 doi:10.1016/j.poly.2016.03.024, IF=2.108
  31. E. Karpova, V. Vasiliev, V. Mamatyuk, N. Polosmak, L. Kundo
    Xiongnu burial complex: A study of ancient textiles from the 22nd Noin-Ula barrow (Mongolia, first century AD)
    Journal of Archaeological Science, V. 70, June 2016, Pp 15-22 doi:10.1016/j.jas.2016.04.001, IF=2.255
  32. M.E. Mironov, I.Yu. Bagryanskaya, E.E. Shults
    Synthesis of 3-trimethylsiloxy-1-(furan-3-yl)butadiene and its reactions with dienophiles
    Chemistry of Heterocyclic Compounds, , 2016, V. 52, N 6, pp 364-373 doi:10.1007/s10593-016-1897-4, IF=0.814
  33. Structure of molecular cocrystals of 18-crown-6 and polyhalogeno-meta-phenylenediamines/ T. A. Vaganova, Yu. V. Gatilov, V. I. Rodionov, E. V. Malykhin// Journal of Structural Chemistry, 2016, V. 57, N 6, pp 1225-1234 doi:10.1134/S002247661606024X, IF=0.536
  34. Reaction of aryl(diarylphosphoryl)methanols with alkyl propiolates. Regio- and stereoselective synthesis of functional vinyl ethers/ N. I. Ivanova, P. A. Volkov, K. O. Khrapova, L. I. Larina, I. Yu. Bagryanskaya, N. K. Gusarova, B. A. Trofimo// Russian Journal of Organic Chemistry, June 2016, V. 52, N. 6, pp 772-776 doi:10.1134/S1070428016060026, IF=0.759
  35. L.S. Konstantinova, I.V. Baranovsky, I.G. Irtegova, I.Y. Bagryanskaya, L.A. Shundrin, A.V. Zibarev, O.A. Rakitin
    Fused 1,2,3-Dithiazoles: Convenient Synthesis, Structural Characterization, and Electrochemical Properties
    Molecules 2016, 21(5), 596 doi:10.3390/molecules21050596, IF=2.464
  36. Valve-containing xenovenous conduit: terra incognita or tabula rasa?/ I.Yu. Zhuravleva, E.V. Karpova, E.V. Kuznetsova, A.S. Yunoshev, A.A. Korobeynikov, T.P. Timchenko, N.R. Nichay, I.A. Soynov, A.V. Gorbatykh// The Siberian Scientific Medical Journal, 2015, V.. 35, № 2, 2015, Pp 90-101
  37. Structure of ultrahigh molecular weight polyethylene-air counterflow flame/ M.B. Gonchikzhapov, A.A. Paletsky, A.G. Tereshchenko, I.K. Shundrina, L.V. Kuibida, A.G. Shmakov, O.P. Korobeinichev// Combustion, Explosion, and Shock Waves, May 2016, V. 52, N 3, pp 260-272 doi:10.1134/S0010508216030023, IF=0.604
  38. I.V. Kulakov, D.N. Ogurtsova, Z.T. Shulgau, T.M. Seilkhanov, Yu.V. Gatilov
    Synthesis and structure of novel ylidene derivatives of methanobenzo[g]thiazolo[2,3-d][1,3,5]oxadiazocine
    Chemistry of Heterocyclic Compounds, 2016, V. 52, N. 5, pp 331-336 doi:10.1007/s10593-016-1886-7, IF=0.814
  39. S.M. Adekenov, A.I. Makubaeva, D.N. Kokkozov, E.N. Kanafin, V.S. Korneev, Yu.V. Gatilov, A.S. Kishkentaeva, G.A. Atazhanova
    Chemical Composition of Artemisia aralensis
    Chemistry of Natural Compounds, 2016, V. 52, N3, pp 417-420 doi:10.1007/s10600-016-1662-z, IF=0.472
  40. I.V. Il'ina, K.P. Volcho, D.V. Korchagina, N.F. Salakhutdinov
    The Convenient Way for Obtaining Geranial by Acid-Catalyzed Kinetic Resolution of Citral
    Helvetica Chimica Acta, 2016, V. 99, N 5, Pp 373-377 doi:10.1002/hlca.201500266, IF=1.87
  41. O.S. Mikhalchenko, D.V. Korchagina, K.P. Volcho, N.F. Salakhutdinov
    A practical way to synthesize chiral fluoro-containing polyhydro-2H-chromenes from monoterpenoids
    Beilstein J. Org. Chem. 2016, 12, 648-653 doi:10.3762/bjoc.12.64, IF=2.697
  42. I.Yu. Bagryanskaya, L.V. Politanskaya, E.V. Tretyakov
    Frequently used, but still unknown: Terbium(III) tris-hexafluoroacetylacetonate dihydrate
    Inorganic Chemistry Communications, April 2016, V. 66, Pp 47-50 doi:10.1016/j.inoche.2016.02.009, IF=1.761
  43. Supramolecular architecture of crystals of perfluorinated 3-alkylphthalides/ T. V. Rybalova, Yu. V. Gatilov, Ya. V. Zonov, V. M. Karpov// Journal of Structural Chemistry, 2016, V. 57, N 4, pp 777-783 doi:10.1134/S0022476616040223, IF=0.536
  44. V.I. Supranovich, A.Yu. Vorob'ev, G.I. Borodkin, Yu.V. Gatilov, V.G. Shubin
    Study on selectivity in the reaction of 2-substituted pyridinium-N-imines with dimethyl acetylenedicarboxylate
    Tetrahedron Letters, V. 57, N 10, 9 March 2016, Pp 1093-1096 doi:10.1016/j.tetlet.2016.01.092, IF=2.346
  45. G.A. Selivanova, E.V. Tretyakov, E.V. Amosov, I.Yu. Bagryanskaya, V.G. Vasiliev, E.V. Vasilyev, V.D. Tikhova, E.V. Karpova, T.V. Basova, D.V. Stass, V.D. Shteingarts
    X-Ray induced phase transitions in 4-((4-(dibutylamino)phenyl)diazenyl)-biphenyl-2,3',4'-tricarbonitrile
    Journal of Molecular Structure, V. 1107, 5 March 2016, Pp 242-248 doi:10.1016/j.molstruc.2015.11.060, IF=1.779
  46. T.P. Kukina, O.I. Sal'nikova, N.K. Khidyrova, M.D. Rakhmatova, N.A. Pankrushina, A.E. Grazhdannikov
    Aliphatic and Terpene Constituents of Alcea nudiflora Extracts
    Chemistry of Natural Compounds, 2016, V.52, N 2, pp 285-287 doi:10.1007/s10600-016-1615-6, IF=0.472
  47. T.F. Mikhailovskaya, A.G. Makarov, N.Yu. Selikhova, A.Yu. Makarov, E.A. Pritchina, I.Yu. Bagryanskaya, E.V. Vorontsova, I.D. Ivanov, V.D. Tikhova, N.P. Gritsan, Y.G. Slizhov, A.V. Zibarev
    Carbocyclic functionalization of quinoxalines, their chalcogen congeners 2,1,3-benzothia/selenadiazoles, and related 1,2-diaminobenzenes based on nucleophilic substitution of fluorine
    Journal of Fluorine Chemistry, V. 183, March 2016, Pp 44-58 doi:10.1016/j.jfluchem.2016.01.009, IF=2.213
  48. D.V. Trukhin, O.Yu. Rogozhnikova, T.I. Troitskaya, V.G. Vasiliev, M.l K. Bowman, V.M. Tormyshev
    Facile and High-Yielding Synthesis of TAM Biradicals and Monofunctional TAM Radicals
    Synlett, 2016, 27(06), Pp 893-899 doi:10.1055/s-0035-1561299, IF=2.322
  49. D.S. Baranov, D.S. Fadeev
    Synthesis of 2-octyloxy-7H-benzo[e]perimidin-7-one and 3-substituted 3H-benzo[e]perimidine-2,7-diones
    Mendeleev Communications, V. 26, N 2, March-April 2016, Pp 174- 176 doi:10.1016/j.mencom.2016.03.032, IF=1.404
  50. S.P. Babailov, P.A. Stabnikov, I.V. Korolkov, N.V. Pervukhina, O.S. Koshcheeva, I.P. Chuikov
    Structure and Paramagnetic Properties of Tris-Pivaloyltrifluoracetonate Thulium(III) Complexes with 18-Crown-6 by X-Ray Analysis and NMR
    Polyhedron, V.105, 17 February 2016, Pp 178-185 doi:10.1016/j.poly.2015.12.014, IF=2.108
  51. M.A. Timoshenko, Yu.V. Kharitonov, M.M. Shakirov, I.Yu. Bagryanskaya, E.E. Shults
    Synthetic Studies on Tricyclic Diterpenoids: Direct Allylic Amination Reaction of Isopimaric Acid Derivatives
    ChemistryOPEN, V. 5, N 1, pp 65-70, February 2016 doi:10.1002/open.201500187, IF=3.585
  52. Т.П. Кукина, Д.Н. Щербаков, К.В. Геньш, Е.А. Тулышева, О.И. Сальникова, А.Е. Гражданников, Е.А. Колосова
    Биоактивные компоненты древесной зелени облепихи HIPPOPHAE RHAMNOIDES L.
    Химия растительного сырья. 2016. № 1. С. 37-42. doi:10.14258/jcprm.2016011100
  53. Reaction of 3-(R-methylidene)-2-ethoxylindolenines with N,N'-binucleophiles/ V. P. Borovik, Yu. V. Gatilov, O. P. Shkurko// Russian Journal of Organic Chemistry, 2016, V. 52, N 2, pp 228-234 doi:10.1134/S1070428016020123, IF=0.759
  54. D.S. Fadeev, I.P. Chuikov, V.I. Mamatyuk
    A study of NMR parameters of para-substituted polyfluorinated benzyl cations and their precursors
    Journal of Fluorine Chemistry, V. 182, February 2016, Pp 53-60 doi:10.1016/j.jfluchem.2015.12.003, IF=2.213
  55. B.A. Trofimov, L.V. Andriyankova, L.P. Nikitina, K.V. Belyaeva, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    (Imidazol-2-yl)methyl-1,3-propanediones: Regioselective C–H Functionalization of the Imidazole Ring by Acylacetylene/Aldehyde Pairs
    EUROPEAN JOURNAL OF ORGANIC CHEMISTRY, 2016, V. 2016, N 6, Pp 1199-1204 doi:10.1002/ejoc.201501617, IF=3.68
  56. B.A. Trofimov, L.P. Nikitina, K.V. Belyaeva, L.V. Andriyankova, A.G. Mal'kina, I.Yu. Bagryanskaya, A.V. Afonin, I.A. Ushakov
    Insertion of 1,3-diphenylprop-2-yn-1-one into imidazo[4,5-b]pyridines in the presence of water: one-pot synthesis of pyrido[2,3-b][1,4]diazocin-9-ones
    Mendeleev Communications, 2016, V.26, N 1, Pp 16-18 doi:10.1016/j.mencom.2016.01.007, IF=1.404
  57. A.V. Artem'ev, S.F. Malysheva, N.K. Gusarova, N.A. Belogorlova, B.G. Sukhov, A.O. Sutyrina, E.A. Matveeva, S.F. Vasilevsky, A.I. Govdi, Yu.V. Gatilov, A.I. Albanov, B.A. Trofimov
    Reaction of elemental phosphorus with &alpa;-methylstyrenes: one-pot synthesis of secondary and tertiary phosphines, prospective bulky ligands for Pd(II) catalysts
    Tetrahedron, V. 72, N 4, 28 January 2016, Pp 443-450 doi:10.1016/j.tet.2015.11.009, IF=2.644
  58. Y.V. Tarasenko, T.V. Abramova, V.I. Mamatuk, V.N. Silnikov
    Effective Synthesis of Fluorescently Labeled Morpholino Nucleoside Triphosphate Derivatives
    Nucleosides, Nucleotides and Nucleic Acids, 2016, V. 35, N 1, Pp 32-42 doi:10.1080/15257770.2015.1114125, IF=0.875
  59. A.V. Shernyukov, A.M. Genaev, G.E. Salnikov, H.S. Rzepa, V.G. Shubin
    Noncatalytic bromination of benzene: A combined computational and experimental study
    Journal of Computational Chemistry, V. 37, N 2, 15 January 2016, Pp 210-225 doi:10.1002/jcc.23985, IF=3.648
  60. Microwave-Assisted Synthesis of Phthalocyanine Zinc Complexes Derived from Aminotricyanobiphenyl-Based Azo Dyes/ G.A. Selivanova, E. V. Amosov, V. G. Vasilyev, E. A. Lukyanets, E. V. Tretyakov, V.D. Shteingarts// Macroheterocycles 2016 9(1) 80-88 doi:10.6060/mhc151192s, IF=0.804
  61. А.Н. Блазнов, Е.В. Атясова, Н.В. Бычин, И.К. Шундрина, Н.Н. Ходакова, В.В. Самойленко
    Влияние степени отверждения связующего на температуру стеклования композитных материалов
    Южно-Сибирский научный вестник, 2016, № 1 (13), С. 13-20.
  62. A.V. Artem'ev, N.A. Chernysheva, S.V. Yas'ko, N.K. Gusarova, I.Yu. Bagryanskaya, B.A. Trofimov
    Straightforward Solvent-Free Synthesis of Tertiary Phosphine Chalcogenides from Secondary Phosphines, Electron-Rich Alkenes, and Elemental Sulfur or Selenium
    HETEROATOM CHEMISTRY, V. 27, N 1, 2016, Pp. 48-53 doi:10.1002/hc.21300, IF=1.202
  63. M.B. Bushuev, D.P. Pishchur, V.A. Logvinenko, Yu.V. Gatilov, I.V. Korolkov, I.K. Shundrina, E.B. Nikolaenkova, V.P. Krivopalov
    A mononuclear iron(II) complex: cooperativity, kinetics and activation energy of the solvent-dependent spin transition
    Dalton Trans., 2016,45(1), 107-120 doi:10.1039/C5DT03750F, IF=4.177
  64. S.P. Babailov, I.P. Chuikov, A.I. Kruppa
    Activation Energies of Intermolecular Dynamics in Ethylenediaminetetraacetate Complexes with Lanthanides: An Effect of the “Gadolinium Break”
    Inorganica Chimica Acta, V. 439, 1 January 2016, Pp 117-122 doi:10.1016/j.ica.2015.10.009, IF=1.917
  65. И.Г. Боярских, А.И. Сысо, В.Г. Васильев, Т.И. Сиромля
    Содержание полифенольных соединений, микро- и макроэлементов в стеблях и листьях LONICERA CAERULEA SUBSP. PALLASII (CAPRIFOLIACEAE)
    Растительные ресурсы. 2016. Т. 52. № 1. С. 135-150


1. Group of Nuclear Magnetic Resonance (GNMR)

- спектроскопия ядерного магнитного резонанса (ЯМР)>
- спектроскопия электронного парамагнитного резонанса (ЭПР) и ЭПР-томография


  • Bruker Avance 300
  • Bruker Avance 400
  • Bruker Avance 600
  • Bruker DRX 500


2. Group of mass spectrometry (GMS)

- газовая хроматография
- газовая хромато-масс-спектроскопия (с приставкой термодесорбции)
- жидкостная хроматография
- жидкостная хромато-масс-спектрометрия


  • Agilent LC 1100 DAD
  • Agilent LC 1200 + Bruker micro TOF-Q
  • Agilent LC 1100 + MSD G2707
  • Agilent 7200 GC-QTOF
  • Agilent GC-MSD 6890/5973
  • HP GC-MSD 5890/5971
  • Thermo Electron DFS GC-MS


3. Group of Optical Spectrometry (GOS)

- ИК-Фурье и КР- спектроскопия
- УФ-Вид спектроскопия
- флуоресцентная спектроскопия
- поляризационная спектроскопия
- электронная микроскопия (с приставкой термодесорбции и элементным анализатором)


  • Varian Cary Eclipse Optical Activity PolАAr 3005
  • Electron microscope Hitachi ТМ-1000 + EDS SFIFT
  • Bruker IR+IR-microscope
  • Vector 22 + IFS-66
  • Bruker Raman Sеnterra
  • НР Uv-Vis 8453А DAD
  • Varian Uv-Vis-NIR Cary 5000
  • Varian Cary Eclipse
  • Optical Activity PolАAr 3005
  • Electron microscope Hitachi ТМ-1000 + EDS SFIFT


4. Group of X-ray analysis (GXRA)

- X- ray diffraction analysis


  • Bruker X-ray САРРА-АРЕХ
  • Bruker X-ray P4


5. Group of thermal analysis (GTA)

- thermal analysis: thermogravimetry and differential scanning calorimetry
- dynamic thermomechanical analysis


  • Thermoanalyzer STA 409
  • Dynamic mechanical DMA-2420

6. Group of service of scientific equipment (GSSE)




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