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Publications in Math-Net.Ru |
Citations |
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2023 |
| 1. |
A. A. Nekrasov, N. V. Nekrasova, M. A. Savel'ev, A. A. Khuzin, V. A. Barachevsky, A. R. Tulyabaev, A. R. Tuktarov, “Electrochemical investigation of a photochromic spiropyran containing a pyrrolidinofullerene moiety”, Mendeleev Commun., 33:4 (2023), 505–508 |
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2022 |
| 2. |
P. V. Karpach, G. T. Vasilyuk, O. V. Venidiktova, V. A. Barachevskiĭ, A. R. Tuktarov, S. A. Maskevich, M. V. Artem'ev, “Luminescence photomodulation of nanospheres with CdSe/ZnS quantum dots in polymer films”, Optics and Spectroscopy, 130:5 (2022), 735–739 |
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2021 |
| 3. |
A. R. Tuktarov, N. M. Chobanov, Z. R. Sadretdinova, R. B. Salikhov, I. N. Mullagaliev, T. R. Salikhov, U. M. Dzhemilev, “New n-type semiconductor material based on styryl fullerene for organic field-effect transistors”, Mendeleev Commun., 31:5 (2021), 641–643 |
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2020 |
| 4. |
A. R. Akhmetov, A. R. Tuktarov, Z. R. Sadretdinova, L. M. Khalilov, U. M. Dzhemilev, “New norbornadiene-tethered fulleropyrrolidines”, Mendeleev Commun., 30:3 (2020), 352–354 |
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| 5. |
U. M. Dzhemilev, A. R. Akhmetov, V. A. D'yakonov, L. U. Dzhemileva, M. M. Yunusbaeva, A. R. Tuktarov, “Synthesis and antitumor activity of methanofullerenes equipped with norbornadiene and quadricyclane moieties”, Mendeleev Commun., 30:2 (2020), 150–152 |
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2019 |
| 6. |
A. R. Tuktarov, A. A. Khuzin, U. M. Dzhemilev, “Acid-base isomerization of hybrid molecules based on fullerene C<sub>60</sub> and spiropyrans”, Mendeleev Commun., 29:2 (2019), 229–231 |
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| 7. |
A. R. Tuktarov, R. B. Salikhov, A. A. Khuzin, I. N. Safargalin, I. N. Mullagaliev, O. V. Venidiktova, T. M. Valova, V. A. Barachevskiĭ, U. M. Dzhemilev, “Optically controlled field effect transistors based on photochromic spiropyran and fullerene C<sub>60</sub> films”, Mendeleev Commun., 29:2 (2019), 160–162 |
21
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| 8. |
O. V. Venidiktova, V. A. Barachevskiĭ, A. A. Khuzin, A. R. Tuktarov, A. I. Shienok, N. L. Zaichenko, “Spectral and kinetic studies of photochromic systems based on graphene and graphene oxide nanostructures”, Optics and Spectroscopy, 127:6 (2019), 1025–1031 ; Optics and Spectroscopy, 127:6 (2019), 1148–1154 |
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2017 |
| 9. |
A. R. Tuktarov, Z. R. Shakirova, L. M. Khalilov, Yu. B. Dudkina, Yu. H. Budnikova, R. B. Salikhov, I. N. Safargalin, U. M. Dzhemilev, “Electrochemical and electrophysical properties of aminomethano- and tetrahydropyridino-C<sub>60</sub>-fullerenes”, Mendeleev Commun., 27:2 (2017), 201–203 |
2
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| 10. |
A. R. Tuktarov, A. A. Khuzin, U. M. Dzhemilev, “Light-controlled molecular switches based on carbon clusters. Synthesis, properties and application prospects”, Usp. Khim., 86:6 (2017), 474–509 ; Russian Chem. Reviews, 86:6 (2017), 474–509 |
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2016 |
| 11. |
A. R. Tuktarov, A. A. Khuzin, A. R. Akhmetov, L. M. Khalilov, A. R. Tulyabaev, V. A. Barachevskiĭ, O. V. Venidiktova, U. M. Dzhemilev, “Covalent binding of fullerene C<sub>60</sub> to dithienylethene as a promising approach to the preparation of new photochromic compounds”, Mendeleev Commun., 26:2 (2016), 143–145 |
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2015 |
| 12. |
A. R. Tuktarov, A. A. Khuzin, L. M. Khalilov, A. R. Tulyabaev, A. R. Akhmetov, U. M. Dzhemilev, “Synthesis of [60]fulleropyrrolidine–dithienylethene conjugates and DFT calculations of their photochromic properties”, Mendeleev Commun., 25:6 (2015), 470–472 |
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| 13. |
A. R. Akhmetov, A. R. Tuktarov, N. R. Porod'ko, U. M. Dzhemilev, “Cycloaddition of alkyl azides to fullerene C<sub>60</sub> in the presence of Cu(OTf)<sub>2</sub>”, Mendeleev Commun., 25:5 (2015), 346–347 |
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| 14. |
A. R. Tuktarov, L. M. Khalilov, K. K. Babievskii, A. R. Akhmetov, V. I. Sokolov, U. M. Dzhemilev, “Circular dichroism spectra of new optically active terpenoid spiro homofullerenes”, Mendeleev Commun., 25:4 (2015), 273–274 |
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2013 |
| 15. |
U. M. Dzhemilev, A. R. Tuktarov, I. R. Yarullin, A. R. Akhmetov, “The reaction of fullerene C<sub>60</sub> with halogen azides”, Mendeleev Commun., 23:6 (2013), 326–328 |
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2010 |
| 16. |
A. R. Tuktarov, U. M. Dzhemilev, “Diazo compounds in the chemistry of fullerenes”, Usp. Khim., 79:7 (2010), 645–671 ; Russian Chem. Reviews, 79:7 (2010), 585–610 |
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