logo nioch.ru


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

Kazantsev M.S.

 

Head of Lab. Dr. Maxim S. Kazantsev

 

e-mail: This email address is being protected from spambots. You need JavaScript enabled to view it.

 



Organic Electronics Laboroatory



The Laboratory history begins from the establishment of the research groups of organic electronic materials in 2013 headed by Dr. Evgeny A. Mostovich.

In 2016 the groups becomes a part of the laboratory of nucleophilic and radical ion reactions.

In 2018 г. the group was included in laboratory of nitrogen compounds.

In 2019 г. organic electronics lab. becomes an independent department headed by Dr. Maxim S. Kazantsev.

RESEARCH AREAS

The main scientific tasks

:

  • Design, synthesis and the study of novel organic optoelectronics materials;
  • The study of molecular and electronics structure of materials;
  • Development of organic light-emitting semiconductors;
  • The study of organic electronics devices;
  • Electrochemical and optical properties of materials;
  • Crystallization, polymorphism, aggregation effects and the study of low-defect organic semiconductors.

 


STAFF

Staff

Employee Position Room Phone Phone in. email Publications
by years
1 Kazantsev Maxim Sergeevich Senior Researcher (Cand. Chem.). Group's Head 240, 239 330-73-87 4-44 (3-68) This email address is being protected from spambots. You need JavaScript enabled to view it.
2 Becker Christina Sergeevna Senior Researcher (Cand. Chem.) 239, 240 330-73-87 3-68, 4-44 This email address is being protected from spambots. You need JavaScript enabled to view it.
3 Sonina Alina Aleksandrovna Researcher 214 НТК 330-78-64 3-64 This email address is being protected from spambots. You need JavaScript enabled to view it.
4 Kuzhelev Andrey Andreevich Researcher (Cand. Chem.) 242 330-55-04 2-05 This email address is being protected from spambots. You need JavaScript enabled to view it.
5 Karmatskih Oleg Yurievich Junior Researcher 335 2-41 This email address is being protected from spambots. You need JavaScript enabled to view it.
6 Koskin Igor Pavlovich Junior Researcher 239, 240 330-73-87 3-68, 4-44 This email address is being protected from spambots. You need JavaScript enabled to view it.
7 Radiush Ekaterina Alekseevna Junior Researcher 221 330-96-64 2-43 This email address is being protected from spambots. You need JavaScript enabled to view it.
8 Shumilov Nikita Alekseevich Junior Researcher 240 This email address is being protected from spambots. You need JavaScript enabled to view it.
9 Shumilov Nikita Alekseevich engineer 240 This email address is being protected from spambots. You need JavaScript enabled to view it.
Students
10 Tolkachev Egor Dmitrievich laboratory assistant 249 This email address is being protected from spambots. You need JavaScript enabled to view it.
11 Cheshkina Darya Sergeevna laboratory assistant
PHD Students
12 Kuimov Anatoly Dmitrievich Junior Researcher 239, 240 330-73-87 3-68, 4-44 This email address is being protected from spambots. You need JavaScript enabled to view it.


Laboratory Partners

Laboratory Partners:


  • Novosibirsk State University;
  • Moscow State University;
  • University of Groningen (Netherlands);
  • Institute of Chemical Kinetics and Combustion;
  • International Tomography Center;
  • Tomsk Polytechnic University;
  • Institute of Synthetic Polymeric Materials;
  • Institute of Semiconductor Physics.


PUBLICATIONS

 

Laboratory staff publications (DB NIOCh)

Reviews, Articles


2021
  1. O.V. Borshchev, M.S. Skorotetcky, V.A. Trukhanov, R.S. Fedorenko, N.M. Surin, E.A. Svidchenko, A.Yu. Sosorev, M.S. Kazantsev, D.Yu. Paraschuk, S.A. Ponomarenko
    Synthesis, characterization and organic field-effect transistors applications of novel tetrathienoacene derivatives
    Dyes and Pigments, Volume 185, Part A, February 2021, 108911 doi:10.1016/j.dyepig.2020.108911, IF=4.612

2020
  1. 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
  2. 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
  3. 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
  4. 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
  5. M. Bretschneider, P. E Spindler, O.Yu. Rogozhnikova, D.V. Trukhin, B. Endeward, A.A. Kuzhelev, E.G. Bagryanskaya, V.M. Tormyshev, T.F. Prisner
    Multi-Quantum Counting of Trityl Radicals
    The Journal of Physical Chemistry Letters, 2020, 11, 15, 6286-6290 doi:10.1021/acs.jpclett.0c01615, IF=6.71
  6. S.A. Amitina, E.V. Zaytseva, N.A. Dmitrieva, A.V. Lomanovich, N.V. Kandalintseva, Yu.A. Ten, I.A. Artamonov, A.F. Markov, D.G. Mazhukin
    5-Aryl-2-(3,5-dialkyl-4-hydroxyphenyl)-4,4-dimethyl-4H-imidazole 3-Oxides and Their Redox Species: How Antioxidant Activity of 1-Hydroxy-2,5-dihydro-1H-imidazoles Correlates with the Stability of Hybrid Phenoxyl-Nitroxides
    Molecules 2020, 25(14), 3118 doi:10.3390/molecules25143118, IF=3.267
  7. From spin-labelled fused polyaromatic compounds to magnetically active graphene nanostructures/ Yu A Ten, N M Troshkova, E V Tretyakov// Russian Chemical reviews, 2020, V. 89, N 7, Pp 693-712 doi:10.1070/RCR4923?locatt=label:RUSSIAN, IF=4.75
  8. P. Fedyushin, T. Rybalova, N. Asanbaeva, E. Bagryanskaya, A. Dmitriev, N. Gritsan, M. Kazantsev, E. Tretyakov
    Synthesis of Nitroxide Diradical Using a New Approach
    Molecules 2020, 25(11), 2701 doi:10.3390/molecules25112701, IF=3.267
  9. Ye. Li, I.P. Koskin, Zh. Ma, E. Benassi, Zh. Wang
    Defect induced photoluminescence and triboluminescence in layered CaLaAl3O7
    Dalton Trans., 2020, V. 49, N 13, Pp 3942-3945 doi:10.1039/C9DT03849C, IF=4.174
  10. 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
  11. E. Zaytseva, D. Shiomi, Yu. Ten, Yu.V. Gatilov, A. Lomanovich, D.V. Stass, A.S. Bogomyakov, A. Yu, K. Sugisaki, K. Sato, T. Takui, E.G. Bagryanskaya, D. Mazhukin
    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
  12. V. Tormyshev, A. Chubarov, O. Krumkacheva, D. Trukhin, O. Rogozhnikova, A. Spitsyna, A. Kuzhelev, V. Koval, M. Fedin, T. Godovikova, M. Bowman, E.G. Bagryanskaya
    Methanethiosulfonate Derivative of OX063 Trityl: a Promising and Efficient Reagent for SDSL of Proteins
    Chemistry-A European Journal, 2020, V.26, N 12, Pp 2705-2712 doi:10.1002/chem.201904587, IF=4.857
  13. 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
  14. A.Yu. Sosorev, V.A. Trukhanov, D.R. Maslennikov, O. V Borshchev, R. Polyakov, M. Skorotetcky, N.M. Surin, M.S. Kazantsev, D.I. Dominskiy, V.A. Tafeenko, S.A. Ponomarenko, D.Yu. Paraschuk
    Fluorinated thiophene-phenylene co-oligomers for optoelectronic devices
    ACS Appl. Mater. Interfaces, 2020, 12, 8, 9507-9519 doi:10.1021/acsami.9b20295, IF=8.758
  15. A.A. Kuzhelev, V.M. Tormyshev, V.F. Plyusnin, O.Yu. Rogozhnikova, M.V. Edeleva, S.L. Veber, E.G. Bagryanskaya
    Photochemistry of tris(2,3,5,6-tetrathiaaryl)methyl radicals in various solutions
    Phys. Chem. Chem. Phys., 2020, V. 22, N 3, Pp 1019-1026 doi:10.1039/C9CP06213K, IF=3.43
  16. 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
    ChemPlusChem, 2020, V. 85, N 1, Pp 159-162 doi:10.1002/cplu.201900709, IF=2.753
  17. Method of preparation of alkylated 1,3-diphenylpropan-2-ones, the components for assembly of graphene nanostructures/ Yu. A. Ten, N. M. Troshkova, E. V. Tretyakov// Russian Chemical Bulletin, 2020, V. 69, Pp 172-175 doi:10.1007/s11172-020-2740-8, IF=1.061

2019
  1. O.A. Krumkacheva, G.Yu. Shevelev, A.A. Lomzov, N.S. Dyrkheeva, A.A. Kuzhelev, V.V. Koval, V.M. Tormyshev, Yu.F. Polienko, M.V. Fedin, D.V. Pyshnyi, O.I. Lavrik, E.G. Bagryanskaya
    DNA complexes with human apurinic/apyrimidinic endonuclease 1: structural insights revealed by pulsed dipolar EPR with orthogonal spin labeling
    Nucleic Acids Research,2019, V. 47, N 15, Pp 7767-7780 doi:10.1093/nar/gkz620, IF=11.147
  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
  3. E. Tretyakov, P. Fedyushin, E. Panteleeva, L. Gurskaya, T. Rybalova, A. Bogomyakov, E. Zaytseva, M. Kazantsev, I. Shundrina, V. Ovcharenko
    Aromatic SNF-Approach to Fluorinated Phenyl tert-Butyl Nitroxides
    Molecules 2019, 24(24), 4493 doi:10.3390/molecules24244493, IF=3.59
  4. A.A. Gorodetskii, T.D. Eubank, B. Driesschaert, M. Poncelet, E. Ellis, V.V. Khramtsov, A.A. Bobko
    Development of multifunctional Overhauser-enhanced magnetic resonance imaging for concurrent in vivo mapping of tumor interstitial oxygenation, acidosis and inorganic phosphate concentration
    Scientific Reports, 2019, V. 9, Issue 1, Art.number 12093 doi:10.1038/s41598-019-48524-3, IF=4.11
  5. 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
  6. 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
  7. 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
  8. 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
  9. D.S. Baranov, O.L. Krivenko, M.S. Kazantsev, D.A. Nevostruev, E.S. Kobeleva, V.A. Zinoviev, A.A. Dmitriev, N.P. Gritsan, L.V. Kulik
    Synthesis of 2,2'-[2,2'-(arenediyl)bis(anthra[2,3-b]thiophene-5,10-diylidene)]tetrapropanedinitriles and their performance as non-fullerene acceptors in organic photovoltaics
    Synthetic Metals, 2019, V. 255, 116097 doi:10.1016/j.synthmet.2019.06.013, IF=2.87
  10. D.S.Baranov,O. L.Krivenko,D. A.Nevostruev,E.M.Glebov,M. N.Uvarov,M. S.Kazantsev,E. A.Mostovich,L. V.Kulik
    2,7-Disubstituted 1,3,6,8-tetraazabenzopyrenes: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2019, V. 168, Pp 219-227 doi:10.1016/j.dyepig.2019.04.062, IF=4.018
  11. 11578/ 11588// doi:10.1039/C9CP00910H, IF=3.567
  12. New Spin Probes: Triand Hexacationic Derivatives of Persistent Tris(tetrathioaryl)methyl Radicals/ D.V. Trukhin, O.Yu.Rogozhnikova, T.I. Troitskaya, A.A, Kuzhelev, E.V. Amosov,H.J. Halpernc, V.V. Koval'b, V.M. Tormyshev// Russian Journal of Organic Chemistry, 2019, V. 55, N 3, pp 296-301 doi:10.1134/S1070428019030035, IF=0.751
  13. A.A. Mannanov, M.S. Kazantsev, A.D. Kuimov, V.G. Konstantinov, D.I. Dominskiy, V.A. Trukhanov, D.S. Anisimov, N.V. Gultikov, V.V. Bruevich, I.P. Koskin, A.A. Sonina, T.V. Rybalova, I.K. Shundrina, E.A. Mostovich, D.Yu. Paraschuk, M.S. Pshenichnikov
    Long-range exciton transport in brightly fluorescent furan/phenylene co-oligomer crystals
    J. Mater. Chem. C, 2019, V. 7, N 1, Pp 60-68 doi:10.1039/C8TC04151B, IF=6.641

2018
  1. Yu.A. Ten, O.G. Salnikov, S.A. Amitina, D.V. Stass, T.V. Rybalova, M.S. Kazantsev, A.S. Bogomyakov, E.A. Mostovich, D.G. Mazhukin
    The Suzuki–Miyaura reaction as a tool for modification of phenoxyl-nitroxyl radicals of the 4H-imidazole N-oxide series
    RSC Adv., 2018, V. 8, N 46, Pp 26099-26107 doi:10.1039/C8RA05103H, IF=2.936
  2. A. A. Sonina, I.P. Koskin, P.S. Sherin, T. V. Rybalova, I. K. Shundrina, E. A. Mostovich, M. S. Kazantsev
    Crystal packing control of a trifluoromethyl-substituted furan/phenylene co-oligomer
    Acta Crystallographica Section B, 2018, V. 74, N 5, Pp 450-457 doi:10.1107/S2052520618011782, IF=6.467
  3. P.V. Petunin, E.A. Martynko, M.E. Trusova, M.S. Kazantsev, T.V. Rybalova, R.R. Valiev, M.N. Uvarov, P.S. Postnikov, E. Mostovich
    Verdazyl radical building blocks: synthesis, structure and Sonogashira cross-coupling reactions
    European Journal of Organic Chemistry, 2018, V. 2018, N 34, Pp 4802-4811 doi:10.1002/ejoc.201701783, IF=2.882
  4. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    A quantitative topological descriptor for linear co-oligomer fusion
    Chem. Commun., 2018, V. 54, N 52, Pp 7235-7238 doi:10.1039/C8CC03156H, IF=6.29
  5. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.A. Nevostruev, E.A. Mostovich, O.V. Antonova, L.V. Kulik
    A Concise and Efficient Route to Electron-Accepting 2,2'-[2,2'-Arenediylbis(11-oxoanthra[1,2-b]thiophene-6-ylidene)]dipropanedinitriles
    European Journal of Organic Chemistry, 2018, V. 2018, N 19, Pp 2259-2266 doi:10.1002/ejoc.201800275, IF=2.882
  6. M.S. Kazantsev, A.A. Beloborodova, A.D. Kuimov, I.P. Koskin, E.S. Frantseva, T.V. Rybalova, I.K. Shundrina, C.S. Becker, E.A. Mostovich
    Synthesis, luminescence and charge transport properties of furan/phenylene co-oligomers: The study of conjugation length effect
    Organic Electronics, , 2018, V. 56, May 2018, Pages 208-215 doi:10.1016/j.orgel.2018.01.010, IF=3.68
  7. L. Gurskaya, I. Bagryanskaya, E. Amosov, M. Kazantsev, L. Politanskaya, E. Zaytseva, E. Bagryanskaya, A. Chernonosov, E. Tretyakov
    1,3-Diaza[3]ferrocenophanes functionalized with a nitronyl nitroxide group
    Tetrahedron, 2018, V. 74, N 15, Pp 1942-1950 doi:10.1016/j.tet.2018.02.062, IF=2.377
  8. D.S. Baranov, M.N. Uvarov, E.M. Glebov, D.A. Nevostruev, M.S. Kazantsev, E.A. Mostovich, D.S. Fadeev, O.V. Antonova, D.E. Utkin, P.A. Kuchinskaya, A.S. Sukhikh, S.A. Gromilov, L.V. Kulik
    1,3,7,9-Tetraazaperylene frameworks: Synthesis, photoluminescence properties, and thin film morphology
    Dyes and Pigments, In Press, V. 150, March 2018, Pp 252-260 doi:10.1016/j.dyepig.2017.12.011, IF=3.767

2017
  1. I.P. Koskin, E.A. Mostovich, E. Benassi, M.S. Kazantsev
    Way to Highly Emissive Materials: Increase of Rigidity by Introduction of a Furan Moiety in Co-Oligomers
    J. Phys. Chem. C, 2017, 121 (42), pp 23359-23369 doi:10.1021/acs.jpcc.7b08305, IF=4.535
  2. M.S. Kazantsev, V.G. Konstantinov, D.I. Dominskiy, V.V. Bruevich, V.A. Postnikov, Y.N. Luponosov, V.A. Tafeenko, N.M. Surin, S.A. Ponomarenko, D.Yu. Paraschuk
    Highly bendable luminescent semiconducting organic single crystal
    Synthetic Metals, V. 232, October 2017, Pp 60-65 doi:10.1016/j.synthmet.2017.07.019, IF=2.434
  3. A.A. Beloborodova, V.S. Minkov, D.A. Rychkov, T.V. Rybalova, E.V. Boldyreva
    First Evidence of Polymorphism in Furosemide Solvates
    Cryst. Growth Des., 2017, 17 (5), pp 2333-2341 doi:10.1021/acs.cgd.6b01191, IF=4.54
  4. M.S. Kazantsev, A.A. Beloborodova, E.S. Frantseva, T.V. Rybalova, V.G. Konstantinov, I.K. Shundrina, D.Yu. Paraschuk, E.A. Mostovich
    Methyl substituent effect on structure, luminescence and semiconducting properties of furan/phenylene co-oligomer single crystals
    CrystEngComm, 2017,19, 1809-1815 doi:10.1039/C6CE02565J, IF=3.108
  5. A.A. Shatrova, D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.M. Glebov, D.S. Fadeev, L.V. Kulik
    Novel Anthrathiophene-Based Small Molecules as Donor Material for Organic Photovoltaics: Synthesis and Light-Induced EPR Study
    Zeitschrift fur Physikalische Chemie, 2017, V. 231, N 2, Pp 425-438 doi:10.1515/zpch-2016-0832, IF=1.327
  6. I. Bagryanskaya, M. Fedin, D. Gorbunov, N. Gritsan, L. Gurskaya, M. Kazantsev, Yu. Polienko, D. Stass, E. Tretyakov
    A Nitroxide Diradical Containing a Ferrocen-1,1'-diyl-substituted 1,3-Diazetidine-2,4-diimine Coupler
    Tetrahedron Letters, 2017, V. 58, N 5, Pp 478-481 doi:10.1016/j.tetlet.2016.12.068, IF=2.193
  7. D.S. Baranov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, Y.V. Gatilov, L.V. Kulik
    Diaza-analogs of benzopyrene and perylene containing thienyl and 4-(phenylamino)phenyl groups: Synthesis, characterization, optical and electrochemical properties
    Dyes and Pigments, 2017, V. 136, Pp 707-714 doi:10.1016/j.dyepig.2016.09.026, IF=3.473

2016
  1. M.S. Kazantsev, E.S. Frantseva, L.G. Kudriashova, V.G. Konstantinov, A.A. Mannanov, T.V. Rybalova, E.V. Karpova, I.K. Shundrina, G.N. Kamaev, M.S. Pshenichnikov, E.A. Mostovich, D.Yu. Paraschuk
    Highly-emissive solution-grown furan/phenylene co-oligomer single crystals
    RSC Adv., 2016,6(95), 92325-92329 doi:10.1039/C6RA23160H, IF=3.289
  2. L.G. Kudryashova, M.S. Kazantsev, V. A. Postnikov, V.V. Bruevich, Y.N. Luponosov, N.M. Surin, O.V. Borshchev, S.A. Ponomarenko, M.S. Pshenichnikov, D.Yu. Paraschuk
    Highly Luminescent Solution-Grown Thiophene-Phenylene Co-Oligomer Single Crystals
    ACS Appl. Mater. Interfaces, 2016, 8 (16), pp 10088-10092 doi:10.1021/acsami.5b11967, IF=7.144

2015
  1. C. Becker, N. Chukanov, I. Grigor’ev
    New amino-bisphosphonate building blocks in the synthesis of bisphosphonic derivatives based on lead compounds
    Phosphorus, Sulfur, and Silicon and the Related Elements, 2015, V. 190, N 7, 1201-1212. 10.1080/10426507.2014.979989 doi:10.1080/10426507.2014.979989, IF=0.561
  2. D.S. Baranov, A.G. Popov, M.N. Uvarov, M.S. Kazantsev, E.A. Mostovich, E.M. Glebov, L.V. Kulik
    Naphtho[4,3,2,1-lmn][2,9]phenanthrolines: Synthesis, сharacterization, optical properties and light-induced electron transfer in composites with the semiconducting polymer MEH-PPV
    Synthetic Metals, V. 201, Pp. 43-48, MAR 2015. doi:10.1016/j.synthmet.2015.01.012, IF=2.252

2013
  1. A. I. Taratayko, C.S. Becker,.I. A. Grigor’ev,Y. V. Gatilov, T. V. Rybalova, V. A. Reznikov
    Synthesis of 3,4-dihydro-2H-pyrrole 1-oxide based aldonitrones as potential spin trapping agents
    Arkivoc 2013, (iv), 272-290.full text doi:10.3998/ark.5550190.p008.159, IF=1.57
  2. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bis-Phosphonic Acid Derivative of Trolox, a New Potential Antioxidant
    Chemistry of Natural Compounds, 2013, V. 49, N 4, P. 785-786. doi:10.1007/s10600-013-0746-2, IF=0.598
  3. K.S. Bekker, N.V. Chukanov, S.A. Popov, I.A. Grigor'ev
    Conjugates of Bisphosphonates with Derivatives of Ursolic, Betulonic, and Betulinic Acids
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 581-582. doi:10.1007/s10600-013-0680-3, IF=0.598
  4. K.S. Bekker, N.V. Chukanov, I.A. Grigor'ev
    Synthesis of a bisphosphonate derivative of folic acid
    Chemistry of Natural Compounds, 2013, V. 49, N 3, P. 495-495. doi:10.1007/s10600-013-0646-5, IF=0.598

Joomla Plugins