(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. Energies 2026, 19 (1), 104. https://doi.org/10.3390/en19010104.

(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. J. Phys. Chem. A 2025, 129 (20), 4458–4470. https://doi.org/10.1021/acs.jpca.5c01243.

(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’ev, A. V. Achieving Deep‐Red TADF with Negative‐Thermal Quenching in [Cu(N^N)(P^P)]⁺ Emitters Through a Perchlorination Strategy. Advanced Optical Materials 2025, e02836. https://doi.org/10.1002/adom.202502836.

(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. The Journal of Physical Chemistry C 2024, 128 (36), 15070–15081. https://doi.org/10.1021/acs.jpcc.4c04297.

(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. International Journal of Molecular Sciences 2023, 24 (4), 4098. https://doi.org/10.3390/ijms24044098.

(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. The Journal of Organic Chemistry 2023, 88 (15), 11003–11009. https://doi.org/10.1021/acs.joc.3c00981.

(7)Shepovalov, K. M.; Benassi, E.; Peshkov, R. Y.; Mostovich, E. A. Symmetric Spirenes: Promising Building Blocks for New Generation Opto-Electronic Materials. Physical Chemistry Chemical Physics 2022, 24 (27), 16836–16851. https://doi.org/10.1039/D2CP01920E.

(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. The Journal of Organic Chemistry 2022, 87 (5), 2456–2469. https://doi.org/10.1021/acs.joc.1c02379.

(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. American journal of cancer research2021, 11 (10), 4668–4682.

(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. ChemPlusChem 2020, 85 (1), 159–162. https://doi.org/10.1002/cplu.201900709.

(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<inf>3</Inf>)<inf>4</Inf>. New Journal of Chemistry 2019, 43 (38). https://doi.org/10.1039/c9nj03361k.

(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. Journal of Materials Chemistry C 2019, 7 (1), 60–68. https://doi.org/10.1039/C8TC04151B.

(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. Materials Chemistry Frontiers 2019, 3 (8), 1545–1554. https://doi.org/10.1039/C9QM00198K.

(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. Dyes and Pigments 2019, 168 (January), 219–227. https://doi.org/10.1016/j.dyepig.2019.04.062.

(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–Miyaura Reaction as a Tool for Modification of Phenoxyl-Nitroxyl Radicals of the 4 H -Imidazole N -Oxide Series. RSC Advances 2018, 8 (46), 26099–26107. https://doi.org/10.1039/C8RA05103H.

(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. Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 2018, 74 (5), 450–457. https://doi.org/10.1107/S2052520618011782.

(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. European Journal of Organic Chemistry 2018, 2018 (34), 4802–4811. https://doi.org/10.1002/ejoc.201701783.

(18)Koskin, I. P.; Mostovich, E. A.; Benassi, E.; Kazantsev, M. S. A Quantitative Topological Descriptor for Linear Co-Oligomer Fusion. Chemical Communications 2018, 54 (52), 7235–7238. https://doi.org/10.1039/C8CC03156H.

(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. Organic Electronics 2018, 56, 208–215. https://doi.org/10.1016/j.orgel.2018.01.010.

(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′-[2,2′-Arenediylbis(11-Oxoanthra[1,2- b ]Thiophene-6-Ylidene)]Dipropanedinitriles. European Journal of Organic Chemistry 2018, 2018 (19), 2259–2266. https://doi.org/10.1002/ejoc.201800275.

(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. Dyes and Pigments 2018, 150, 252–260. https://doi.org/10.1016/j.dyepig.2017.12.011.

(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. The Journal of Physical Chemistry C 2017, 121(42), 23359–23369. https://doi.org/10.1021/acs.jpcc.7b08305.

(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. CrystEngComm 2017, 19 (13), 1809–1815. https://doi.org/10.1039/C6CE02565J.

(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. Journal of Materials Chemistry C 2017, 5 (35), 9053–9065. https://doi.org/10.1039/C7TC03357E.

(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. Dyes and Pigments 2017, 136, 707–714. https://doi.org/10.1016/j.dyepig.2016.09.026.

(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. RSC Adv. 2016, 6 (95), 92325–92329. https://doi.org/10.1039/C6RA23160H.

(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, Сharacterization, Optical Properties and Light-Induced Electron Transfer in Composites with the Semiconducting Polymer MEH-PPV. Synthetic Metals 2015, 201, 43–48. https://doi.org/10.1016/j.synthmet.2015.01.012.

(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–1/2 Dimers. Journal of Materials Chemistry C 2014, 2 (32), 6618. https://doi.org/10.1039/C4TC00399C.

(29)Mostovich, E. A.; Borozdina, Y.; Enkelmann, V.; Remović-Langer, K.; Wolf, B.; Lang, M.; Baumgarten, M. Planar Biphenyl-Bridged Biradicals as Building Blocks for the Design of Quantum Magnets. Crystal Growth & Design 2012, 12 (1), 54–59. https://doi.org/10.1021/cg201224g.

(30)Mostovich, E. A.; Mazhukin, D. G.; Rybalova, T. V. Reactions of Vicinal Aliphatic Bis ( Hydroxylamines ) with Trifunctionalized Methane Derivatives. Arkivoc 2011, 2011 (xi), 29–42.

(31)Wolf, B.; Cong, P. T.; Remović-Langer, K.; Borozdina, Y. D.; Mostovich, E.; Baumgarten, M.; Lang, M. Coupled Spin S = 1/2 Dimer Systems Based on Nitronyl-Nitroxide Biradicals. Journal of Physics: Conference Series 2010, 200 (1), 012225. https://doi.org/10.1088/1742-6596/200/1/012225.

(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. Mendeleev Communications 2007, 17 (1), 48–50. https://doi.org/10.1016/j.mencom.2007.01.019.