{"id":28,"date":"2019-05-25T12:42:23","date_gmt":"2019-05-25T09:42:23","guid":{"rendered":"http:\/\/orellab.nsu.ru\/?page_id=28"},"modified":"2026-04-23T13:22:13","modified_gmt":"2026-04-23T06:22:13","slug":"publications","status":"publish","type":"page","link":"http:\/\/orellab.nsu.ru\/?page_id=28","title":{"rendered":"Publications"},"content":{"rendered":"\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p>(1)Baranov, D. S.; Kobeleva, E. S.; Uvarov, M. N.; Molchanov, I. A.; Dmitriev, A. A.; Kazantsev, M. S.; Sysoev, V. I.; Sukhikh, A. S.; Mostovich, E. A.; Kulik, L. V. Exciton Self-Splitting: One More Reason for Poor Photovoltaic Performance of Non-Fullerene Acceptors.\u00a0<em>Energies<\/em>\u00a0<strong>2026<\/strong>,\u00a0<em>19<\/em>\u00a0(1), 104.\u00a0<a href=\"https:\/\/doi.org\/10.3390\/en19010104\">https:\/\/doi.org\/10.3390\/en19010104<\/a>.<\/p>\n\n\n\n<p>(2)Tarakanovskaya, D. D.; Mostovich, E. A. Quantum-Chemical Simulation of Multiresonance Thermally Activated Delayed Fluorescence Materials Based on B,N-Heteroarenes Using Graph Neural Networks.\u00a0<em>J. Phys. Chem. A<\/em>\u00a0<strong>2025<\/strong>,\u00a0<em>129<\/em>\u00a0(20), 4458\u20134470.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acs.jpca.5c01243\">https:\/\/doi.org\/10.1021\/acs.jpca.5c01243<\/a>.<\/p>\n\n\n\n<p>(3)Petyuk, M. Yu.; Sukhikh, T. S.; Stass, D. V.; Carignan, G. M.; Rakhmanova, M. I.; Doronina, E. P.; Sokolov, M. N.; Mostovich, E. A.; Bagryanskaya, I. Yu.; Li, J.; Artem\u2019ev, A. V. Achieving Deep\u2010Red TADF with Negative\u2010Thermal Quenching in [Cu(N^N)(P^P)]<sup>+<\/sup>\u00a0Emitters Through a Perchlorination Strategy.\u00a0<em>Advanced Optical Materials<\/em>\u00a0<strong>2025<\/strong>, e02836.\u00a0<a href=\"https:\/\/doi.org\/10.1002\/adom.202502836\">https:\/\/doi.org\/10.1002\/adom.202502836<\/a>.<\/p>\n\n\n\n<p>(4)Cheshkina, D. S.; Becker, C. S.; Sonina, A. A.; Koskin, I. P.; Shundrina, I. K.; Mostovich, E. A.; Kazantsev, M. S. Rigid Planar Aggregation-Induced Emission-Active Conjugated Molecule.\u00a0<em>The Journal of Physical Chemistry C<\/em>\u00a0<strong>2024<\/strong>,\u00a0<em>128<\/em>\u00a0(36), 15070\u201315081.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acs.jpcc.4c04297\">https:\/\/doi.org\/10.1021\/acs.jpcc.4c04297<\/a>.<\/p>\n\n\n\n<p>(5)Uvarov, M. N.; Kobeleva, E. S.; Degtyarenko, K. M.; Zinovyev, V. A.; Popov, A. A.; Mostovich, E. A.; Kulik, L. V. Fast Recombination of Charge-Transfer State in Organic Photovoltaic Composite of P3HT and Semiconducting Carbon Nanotubes Is the Reason for Its Poor Photovoltaic Performance.\u00a0<em>International Journal of Molecular Sciences<\/em>\u00a0<strong>2023<\/strong>,\u00a0<em>24<\/em>\u00a0(4), 4098.\u00a0<a href=\"https:\/\/doi.org\/10.3390\/ijms24044098\">https:\/\/doi.org\/10.3390\/ijms24044098<\/a>.<\/p>\n\n\n\n<p>(6)Ivanov, K. S.; Samburskiy, D. E.; Zargarova, L. V.; Komarov, V. Y.; Mostovich, E. A. Construction of Annulated Spiro[4.4]-Nonane-Diones via the Tandem [4 + 2]-Cycloaddition\/Aromatization Reaction.\u00a0<em>The Journal of Organic Chemistry<\/em>\u00a0<strong>2023<\/strong>,\u00a0<em>88<\/em>\u00a0(15), 11003\u201311009.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.3c00981\">https:\/\/doi.org\/10.1021\/acs.joc.3c00981<\/a>.<\/p>\n\n\n\n<p>(7)Shepovalov, K. M.; Benassi, E.; Peshkov, R. Y.; Mostovich, E. A. Symmetric Spirenes: Promising Building Blocks for New Generation Opto-Electronic Materials.\u00a0<em>Physical Chemistry Chemical Physics<\/em>\u00a0<strong>2022<\/strong>,\u00a0<em>24<\/em>\u00a0(27), 16836\u201316851.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/D2CP01920E\">https:\/\/doi.org\/10.1039\/D2CP01920E<\/a>.<\/p>\n\n\n\n<p>(8)Ivanov, K. S.; Riesebeck, T.; Skolyapova, A.; Liakisheva, I.; Kazantsev, M. S.; Sonina, A. A.; Peshkov, R. Y.; Mostovich, E. A. P 2 O 5 -Promoted Cyclization of Di[Aryl(Hetaryl)Methyl] Malonic Acids as a Pathway to Fused Spiro[4.4]Nonane-1,6-Diones.\u00a0<em>The Journal of Organic Chemistry<\/em>\u00a0<strong>2022<\/strong>,\u00a0<em>87<\/em>\u00a0(5), 2456\u20132469.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.1c02379\">https:\/\/doi.org\/10.1021\/acs.joc.1c02379<\/a>.<\/p>\n\n\n\n<p>(9)Zharkov, D. O.; Yudkina, A. V.; Riesebeck, T.; Loshchenova, P. S.; Mostovich, E. A.; Dianov, G. L. Boron-Containing Nucleosides as Tools for Boron-Neutron Capture Therapy.\u00a0<em>American journal of cancer research<\/em><strong>2021<\/strong>,\u00a0<em>11<\/em>\u00a0(10), 4668\u20134682.<\/p>\n\n\n\n<p>(10)Petunin, P. V.; Rybalova, T. V.; Trusova, M. E.; Uvarov, M. N.; Kazantsev, M. S.; Mostovich, E. A.; Postulka, L.; Eibisch, P.; Wolf, B.; Lang, M.; Postnikov, P. S.; Baumgarten, M. A Weakly Antiferromagnetically Coupled Biradical Combining Verdazyl with Nitronylnitroxide Units.\u00a0<em>ChemPlusChem<\/em>\u00a0<strong>2020<\/strong>,\u00a0<em>85<\/em>\u00a0(1), 159\u2013162.\u00a0<a href=\"https:\/\/doi.org\/10.1002\/cplu.201900709\">https:\/\/doi.org\/10.1002\/cplu.201900709<\/a>.<\/p>\n\n\n\n<p>(11)Petunin, P. V.; Votkina, D. E.; Trusova, M. E.; Rybalova, T. V.; Amosov, E. V.; Uvarov, M. N.; Postnikov, P. S.; Kazantsev, M. S.; Mostovich, E. A. Oxidative Addition of Verdazyl Halogenides to Pd(PPh&lt;inf>3&lt;\/Inf>)&lt;inf>4&lt;\/Inf>.\u00a0<em>New Journal of Chemistry<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em>43<\/em>\u00a0(38).\u00a0<a href=\"https:\/\/doi.org\/10.1039\/c9nj03361k\">https:\/\/doi.org\/10.1039\/c9nj03361k<\/a>.<\/p>\n\n\n\n<p>(12)Mannanov, A. A.; Kazantsev, M. S.; Kuimov, A. D.; Konstantinov, V. G.; Dominskiy, D. I.; Trukhanov, V. A.; Anisimov, D. S.; Gultikov, N. V.; Bruevich, V. V.; Koskin, I. P.; Sonina, A. A.; Rybalova, T. V.; Shundrina, I. K.; Mostovich, E. A.; Paraschuk, D. Y.; Pshenichnikov, M. S. Long-Range Exciton Transport in Brightly Fluorescent Furan\/Phenylene Co-Oligomer Crystals.\u00a0<em>Journal of Materials Chemistry C<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em>7<\/em>\u00a0(1), 60\u201368.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C8TC04151B\">https:\/\/doi.org\/10.1039\/C8TC04151B<\/a>.<\/p>\n\n\n\n<p>(13)Kazantsev, M. S.; Sonina, A. A.; Koskin, I. P.; Sherin, P. S.; Rybalova, T. V.; Benassi, E.; Mostovich, E. A. Stimuli Responsive Aggregation-Induced Emission of Bis(4-((9 H -Fluoren-9-Ylidene)Methyl)Phenyl)Thiophene Single Crystals.\u00a0<em>Materials Chemistry Frontiers<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em>3<\/em>\u00a0(8), 1545\u20131554.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C9QM00198K\">https:\/\/doi.org\/10.1039\/C9QM00198K<\/a>.<\/p>\n\n\n\n<p>(14)Baranov, D. S.; Krivenko, O. L.; Nevostruev, D. A.; Glebov, E. M.; Uvarov, M. N.; Kazantsev, M. S.; Mostovich, E. A.; Kulik, L. V. 2,7-Disubstituted 1,3,6,8-Tetraazabenzopyrenes: Synthesis, Characterization, Optical and Electrochemical Properties.\u00a0<em>Dyes and Pigments<\/em>\u00a0<strong>2019<\/strong>,\u00a0<em>168<\/em>\u00a0(January), 219\u2013227.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.dyepig.2019.04.062\">https:\/\/doi.org\/10.1016\/j.dyepig.2019.04.062<\/a>.<\/p>\n\n\n\n<p>(15)Ten, Y. A.; Salnikov, O. G.; Amitina, S. A.; Stass, D. V.; Rybalova, T. V.; Kazantsev, M. S.; Bogomyakov, A. S.; Mostovich, E. A.; Mazhukin, D. G. The Suzuki\u2013Miyaura Reaction as a Tool for Modification of Phenoxyl-Nitroxyl Radicals of the 4 H -Imidazole N -Oxide Series.\u00a0<em>RSC Advances<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>8<\/em>\u00a0(46), 26099\u201326107.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C8RA05103H\">https:\/\/doi.org\/10.1039\/C8RA05103H<\/a>.<\/p>\n\n\n\n<p>(16)Sonina, A. A.; Koskin, I. P.; Sherin, P. S.; Rybalova, T. V.; Shundrina, I. K.; Mostovich, E. A.; Kazantsev, M. S. Crystal Packing Control of a Trifluoromethyl-Substituted Furan\/Phenylene Co-Oligomer.\u00a0<em>Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>74<\/em>\u00a0(5), 450\u2013457.\u00a0<a href=\"https:\/\/doi.org\/10.1107\/S2052520618011782\">https:\/\/doi.org\/10.1107\/S2052520618011782<\/a>.<\/p>\n\n\n\n<p>(17)Petunin, P. V.; Martynko, E. A.; Trusova, M. E.; Kazantsev, M. S.; Rybalova, T. V.; Valiev, R. R.; Uvarov, M. N.; Mostovich, E. A.; Postnikov, P. S. Verdazyl Radical Building Blocks: Synthesis, Structure, and Sonogashira Cross-Coupling Reactions.\u00a0<em>European Journal of Organic Chemistry<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>2018<\/em>\u00a0(34), 4802\u20134811.\u00a0<a href=\"https:\/\/doi.org\/10.1002\/ejoc.201701783\">https:\/\/doi.org\/10.1002\/ejoc.201701783<\/a>.<\/p>\n\n\n\n<p>(18)Koskin, I. P.; Mostovich, E. A.; Benassi, E.; Kazantsev, M. S. A Quantitative Topological Descriptor for Linear Co-Oligomer Fusion.\u00a0<em>Chemical Communications<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>54<\/em>\u00a0(52), 7235\u20137238.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C8CC03156H\">https:\/\/doi.org\/10.1039\/C8CC03156H<\/a>.<\/p>\n\n\n\n<p>(19)Kazantsev, M. S.; Beloborodova, A. A.; Kuimov, A. D.; Koskin, I. P.; Frantseva, E. S.; Rybalova, T. V.; Shundrina, I. K.; Becker, C. S.; Mostovich, E. A. Synthesis, Luminescence and Charge Transport Properties of Furan\/Phenylene Co-Oligomers: The Study of Conjugation Length Effect.\u00a0<em>Organic Electronics<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>56<\/em>, 208\u2013215.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.orgel.2018.01.010\">https:\/\/doi.org\/10.1016\/j.orgel.2018.01.010<\/a>.<\/p>\n\n\n\n<p>(20)Baranov, D. S.; Uvarov, M. N.; Kazantsev, M. S.; Glebov, E. M.; Nevostruev, D. A.; Mostovich, E. A.; Antonova, O. V.; Kulik, L. V. A Concise and Efficient Route to Electron-Accepting 2,2\u2032-[2,2\u2032-Arenediylbis(11-Oxoanthra[1,2- b ]Thiophene-6-Ylidene)]Dipropanedinitriles.\u00a0<em>European Journal of Organic Chemistry<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>2018<\/em>\u00a0(19), 2259\u20132266.\u00a0<a href=\"https:\/\/doi.org\/10.1002\/ejoc.201800275\">https:\/\/doi.org\/10.1002\/ejoc.201800275<\/a>.<\/p>\n\n\n\n<p>(21)Baranov, D. S.; Uvarov, M. N.; Glebov, E. M.; Nevostruev, D. A.; Kazantsev, M. S.; Mostovich, E. A.; Fadeev, D. S.; Antonova, O. V.; Utkin, D. E.; Kuchinskaya, P. A.; Sukhikh, A. S.; Gromilov, S. A.; Kulik, L. V. 1,3,7,9-Tetraazaperylene Frameworks: Synthesis, Photoluminescence Properties, and Thin Film Morphology.\u00a0<em>Dyes and Pigments<\/em>\u00a0<strong>2018<\/strong>,\u00a0<em>150<\/em>, 252\u2013260.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.dyepig.2017.12.011\">https:\/\/doi.org\/10.1016\/j.dyepig.2017.12.011<\/a>.<\/p>\n\n\n\n<p>(22)Koskin, I. P.; Mostovich, E. A.; Benassi, E.; Kazantsev, M. S. Way to Highly Emissive Materials: Increase of Rigidity by Introduction of a Furan Moiety in Co-Oligomers.\u00a0<em>The Journal of Physical Chemistry C<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>121<\/em>(42), 23359\u201323369.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/acs.jpcc.7b08305\">https:\/\/doi.org\/10.1021\/acs.jpcc.7b08305<\/a>.<\/p>\n\n\n\n<p>(23)Kazantsev, M. S.; Beloborodova, A. A.; Frantseva, E. S.; Rybalova, T. V.; Konstantinov, V. G.; Shundrina, I. K.; Paraschuk, D. Y.; Mostovich, E. A. Methyl Substituent Effect on Structure, Luminescence and Semiconducting Properties of Furan\/Phenylene Co-Oligomer Single Crystals.\u00a0<em>CrystEngComm<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>19<\/em>\u00a0(13), 1809\u20131815.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C6CE02565J\">https:\/\/doi.org\/10.1039\/C6CE02565J<\/a>.<\/p>\n\n\n\n<p>(24)Borozdina, Y. B.; Mostovich, E. A.; Cong, P. T.; Postulka, L.; Wolf, B.; Lang, M.; Baumgarten, M. Spin-Dimer Networks: Engineering Tools to Adjust the Magnetic Interactions in Biradicals.\u00a0<em>Journal of Materials Chemistry C<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>5<\/em>\u00a0(35), 9053\u20139065.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C7TC03357E\">https:\/\/doi.org\/10.1039\/C7TC03357E<\/a>.<\/p>\n\n\n\n<p>(25)Baranov, D. S.; Uvarov, M. N.; Kazantsev, M. S.; Mostovich, E. A.; Glebov, E. M.; Gatilov, Y. V.; Kulik, L. V. Diaza-Analogs of Benzopyrene and Perylene Containing Thienyl and 4-(Phenylamino)Phenyl Groups: Synthesis, Characterization, Optical and Electrochemical Properties.\u00a0<em>Dyes and Pigments<\/em>\u00a0<strong>2017<\/strong>,\u00a0<em>136<\/em>, 707\u2013714.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.dyepig.2016.09.026\">https:\/\/doi.org\/10.1016\/j.dyepig.2016.09.026<\/a>.<\/p>\n\n\n\n<p>(26)Kazantsev, M. S.; Frantseva, E. S.; Kudriashova, L. G.; Konstantinov, V. G.; Mannanov, A. A.; Rybalova, T. V.; Karpova, E. V.; Shundrina, I. K.; Kamaev, G. N.; Pshenichnikov, M. S.; Mostovich, E. A.; Paraschuk, D. Y. Highly-Emissive Solution-Grown Furan\/Phenylene Co-Oligomer Single Crystals.\u00a0<em>RSC Adv.<\/em>\u00a0<strong>2016<\/strong>,\u00a0<em>6<\/em>\u00a0(95), 92325\u201392329.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C6RA23160H\">https:\/\/doi.org\/10.1039\/C6RA23160H<\/a>.<\/p>\n\n\n\n<p>(27)Baranov, D. S.; Popov, A. G.; Uvarov, M. N.; Kazantsev, M. S.; Mostovich, E. A.; Glebov, E. M.; Kulik, L. V. Naphtho[4,3,2,1-Lmn][2,9]Phenanthrolines: Synthesis, \u0421haracterization, Optical Properties and Light-Induced Electron Transfer in Composites with the Semiconducting Polymer MEH-PPV.\u00a0<em>Synthetic Metals<\/em>\u00a0<strong>2015<\/strong>,\u00a0<em>201<\/em>, 43\u201348.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.synthmet.2015.01.012\">https:\/\/doi.org\/10.1016\/j.synthmet.2015.01.012<\/a>.<\/p>\n\n\n\n<p>(28)Borozdina, Y. B.; Mostovich, E.; Enkelmann, V.; Wolf, B.; Cong, P. T.; Tutsch, U.; Lang, M.; Baumgarten, M. Interacting Networks of Purely Organic Spin\u20131\/2 Dimers.\u00a0<em>Journal of Materials Chemistry C<\/em>\u00a0<strong>2014<\/strong>,\u00a0<em>2<\/em>\u00a0(32), 6618.\u00a0<a href=\"https:\/\/doi.org\/10.1039\/C4TC00399C\">https:\/\/doi.org\/10.1039\/C4TC00399C<\/a>.<\/p>\n\n\n\n<p>(29)Mostovich, E. A.; Borozdina, Y.; Enkelmann, V.; Removi\u0107-Langer, K.; Wolf, B.; Lang, M.; Baumgarten, M. Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets.\u00a0<em>Crystal Growth &amp; Design<\/em>\u00a0<strong>2012<\/strong>,\u00a0<em>12<\/em>\u00a0(1), 54\u201359.\u00a0<a href=\"https:\/\/doi.org\/10.1021\/cg201224g\">https:\/\/doi.org\/10.1021\/cg201224g<\/a>.<\/p>\n\n\n\n<p>(30)Mostovich, E. A.; Mazhukin, D. G.; Rybalova, T. V. Reactions of Vicinal Aliphatic Bis ( Hydroxylamines ) with Trifunctionalized Methane Derivatives.\u00a0<em>Arkivoc<\/em>\u00a0<strong>2011<\/strong>,\u00a0<em>2011<\/em>\u00a0(xi), 29\u201342.<\/p>\n\n\n\n<p>(31)Wolf, B.; Cong, P. T.; Removi\u0107-Langer, K.; Borozdina, Y. D.; Mostovich, E.; Baumgarten, M.; Lang, M. Coupled Spin S = 1\/2 Dimer Systems Based on Nitronyl-Nitroxide Biradicals.\u00a0<em>Journal of Physics: Conference Series<\/em>\u00a0<strong>2010<\/strong>,\u00a0<em>200<\/em>\u00a0(1), 012225.\u00a0<a href=\"https:\/\/doi.org\/10.1088\/1742-6596\/200\/1\/012225\">https:\/\/doi.org\/10.1088\/1742-6596\/200\/1\/012225<\/a>.<\/p>\n\n\n\n<p>(32)Mostovich, E. A.; Mazhukin, D. G.; Gatilov, Y. V.; Rybalova, T. V. Coupling of 1,2-Bis(Alkoxyamino)Cyclohexanes with 1,3-Dicarbonyl Compounds: First Synthesis of 1,4-Dialkoxy-2,3-Dihydro-1,4-Diazepinium Salts.\u00a0<em>Mendeleev Communications<\/em>\u00a0<strong>2007<\/strong>,\u00a0<em>17<\/em>\u00a0(1), 48\u201350.\u00a0<a href=\"https:\/\/doi.org\/10.1016\/j.mencom.2007.01.019\">https:\/\/doi.org\/10.1016\/j.mencom.2007.01.019<\/a>.<\/p>\n<\/div>\n<\/div>\n\n\n\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\"><\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\"><\/div>\n<\/div>\n","protected":false},"excerpt":{"rendered":"<p>(1)Baranov, D. S.; Kobeleva, E. S.; Uvarov, M. N.; Molchanov, I. A.; Dmitriev, A. A.; Kazantsev, M. S.; Sysoev, V. [&hellip;]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-28","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/pages\/28","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=28"}],"version-history":[{"count":13,"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/pages\/28\/revisions"}],"predecessor-version":[{"id":1308,"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=\/wp\/v2\/pages\/28\/revisions\/1308"}],"wp:attachment":[{"href":"http:\/\/orellab.nsu.ru\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=28"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}