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A Markovskyi; P Radomski; W Dewo; V Gorbenko; A Fedorov; T Runka; Y Zorenko, Photoluminescence and Raman spectroscopy of Ce3+ doped Y3Al5O12 single crystalline films grown onto Y3Al5O12 and Lu3Al5O12 substrates, Materials Research Bulletin, 2025, 182, DOI: 10.1016/j.materresbull.2024.113141
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A Y Chumak; D O Tarasenko; O O Kolomoitsev; V M Kotlyar; S V Shishkina; A O Doroshenko, Thiazolic analogs of 3-OH-chromone: Synthesis, molecular structure, fluorescence spectra and photophysics, Journal of Molecular Structure, 2025, 1328, DOI: 10.1016/j.molstruc.2025.141357
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V Sachok; N Kariaka; V Trush; O Horniichuk; O Korovin; N Rusakova; V Dyakonenko; S Shishkina; M Lazarenko; V Amirkhanov, Novel bis-carbacylamidophosphate and its complexes of rare earth elements, Inorganica Chimica Acta, 2025, 577, DOI: 10.1016/j.ica.2024.122515
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A O Poliudov; D Y Havryshko; M D Sorokin; A V Yatsymyrskyi; P A Virych; S V Shishkina; A A Fokin; Т V Omelian; A I Kysil; D S Milokhov; A V Dobrydnev, Synthesis, tautomerism, and anticancer activity of 5,5-disubstituted 1,2-oxathiolan-4-one 2,2-dioxides, Journal of Molecular Structure, 2025, 1325, DOI: 10.1016/j.molstruc.2024.140952
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Oleksii O. Demidov; Ludmila V. Chepeleva; Svitlana V. Shishkina; Eugene S. Gladkov; Alexander Kyrychenko; Rostyslav P. Linnik; Alexander D. Roshal, Influence of C3′- and C4′-substitutions on fluorescence, crystal packing, and physicochemical properties of flavonol, RSC Advances, 2025, 15 (43), 36300-36318, DOI: 10.1039/D5RA05790F
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Alexander V. Tsygankov; Tetiana O. Savluk; Vladyslav O. Vereshchak; Svitlana V. Shishkina; Oleksandr V. Buravov; Valentyn A. Chebanov, Synthesis of Morpholine‐2,5‐Diones by Tandem of Azido‐Ugi and Ugi Reactions, European Journal of Organic Chemistry, 2025, 28 (33), DOI: 10.1002/ejoc.202500414
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Svitlana V. Shishkina; Anna M. Shaposhnyk; Viktoriya V. Dyakonenko; Mariia O. Shyshkina; Sergiy M. Kovalenko, Use of quantum chemical methods to study concomitant polymorphs of a new benzimidazole-1,2,3-triazole hybrid compound, CrystEngComm, 2024, 26 (10), 1481-1493, DOI: 10.1039/D3CE01152F
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S V Shishkina; A M Shaposhnyk; I S Konovalova; V V Dyakonenko; Y O Vaksler, Concomitant polymorphs of 2-imino-2H-chromene-3-carboxylic acid amide: experimental and quantum chemical study, Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 2024, 80 (Pt 1), 27-37, DOI: 10.1107/S2052520623010193
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I S Konovalova; S V Shishkina; M Wyshusek; M Patzer; G J Reiss, Supramolecular architecture of theophylline polymorphs, monohydrate and co-crystals with iodine: study from the energetic viewpoint, RSC Advances, 2024, 14 (41), 29774-29788, DOI: 10.1039/d4ra04368e
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Y O Chuchvera; V Tararina; I Chuchvera; E N Ostapchuk; M V Popova; S V Shishkina; Y M Volovenko; A V Dobrydnev, Synthesis of α-Phenyl β-Enamino γ-Sultims: The New Horizon of the CSIC Reaction, Synlett, 2024, 36 (1), 92-96, DOI: 10.1055/s-0043-1763751
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S V Shishkina; A M Shaposhnyk; V V Dyakonenko; M O Shyshkina; S M Kovalenko, Use of quantum chemical methods to study concomitant polymorphs of a new benzimidazole-1,2,3-triazole hybrid compound, CrystEngComm, 2024, 26 (10), 1481-1493, DOI: 10.1039/d3ce01152f
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Oleg A. Zhikol; Daria Yu. Miasnikova; Olga V. Vashchenko; Natalia A. Pinchukova; Oleksandr I. Zbruyev; Svitlana V. Shishkina; Alexander Kyrychenko; Valentyn A. Chebanov, Host-guest complexation of (pyridinyltriazolylthio) acetic acid with cucurbit[n]urils (n=6,7,8): Molecular calculations and thermogravimetric analysis, Journal of Molecular Structure, 2023, 1294, 136532, DOI: 10.1016/j.molstruc.2023.136532
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S V Shishkina; A M Shaposhnik; V V Dyakonenko; V M Baumer; V V Rudiuk; I B Yanchuk; I A Levandovskiy, New Polymorphic Modifications of 6-Methyluracil: An Experimental and Quantum Chemical Study, ACS Omega, 2023, 8 (23), 20661-20674, DOI: 10.1021/acsomega.3c01231
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S V Shishkina; A M Shaposhnyk; V N Baumer; N I Voloshchuk; P S Bondarenko; I V Ukrainets, 1-Allyl-4-hydroxy-2,2-dioxo-N-(4-methoxyphenyl)-1H-2λ6,1-benzothiazine-3-carboxamide: Polymorphic transition due to grinding with the loss of the biological activity, Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 2022, 78, 70-79, DOI: 10.1107/S2052520621013093
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S V Shishkina; V V Dyakonenko; O V Shishkin; V P Semynozhenko; T Y Bogashchenko; A Y Lyapunov; T I Kirichenko, Halogen…π interactions in the complexes of fluorenonophane with haloforms, Structural Chemistry, 2022, 33 (1), 257-266, DOI: 10.1007/s11224-021-01839-2
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S V Shishkina; Y A Vaksler; I S Konovalova; V V Dyakonenko; V V Varchenko, Quantum Chemical Study on Mefenamic Acid Polymorphic Forms, ACS Omega, 2022, 7 (21), 17544-17554, DOI: 10.1021/acsomega.1c06967
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Y A Vaksler; A Idrissi; S V Shishkina, Is it possible to predict the stability of a crystal structure under the influence of pressure? Quantum chemical study of ibuprofen crystals, New Journal of Chemistry, 2022, 46 (8), 3856-3865, DOI: 10.1039/d1nj05780d
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I S Konovalova; A M Shaposhnyk; V N Baumer; B A Chalyk; S V Shishkina, Polymorphic transition due to grinding: the case of 3-[1-(tert-butoxycarbonyl)azetidin-3-yl]-1,2-oxazole-4-carboxylic acid, Acta crystallographica Section B, Structural science, crystal engineering and materials, 2022, 78 (Pt 3 Pt 2), 510-519, DOI: 10.1107/S2052520622003900
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Y Vaksler; A Idrissi; S V Shishkina, High-Pressure Influence on Piracetam Crystals: Studying by Quantum Chemical Methods, Crystal Growth and Design, 2021, 21 (10), 5697-5711, DOI: 10.1021/acs.cgd.1c00534
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S V Shishkina; V N Baumer; S M Kovalenko; P V Trostianko; N D Bunyatyan, Usage of Quantum Chemical Methods to Understand the Formation of Concomitant Polymorphs of Acetyl 2-(N-(2-Fluorophenyl)imino)coumarin-3-carboxamide, ACS Omega, 2021, 6 (4), 3120-3129, DOI: 10.1021/acsomega.0c05516
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V V Rudiuk; A M Shaposhnyk; V M Baumer; I A Levandovskiy; S V Shishkina, Salts of 4-[(benzylamino)carbonyl]-1-methylpyridinium and iodide anions with different cation:iodine stoichiometric ratios, Acta Crystallographica Section E: Crystallographic Communications, 2021, 77, 1219-1223, DOI: 10.1107/S2056989021011300
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I S Konovalova; E N Muzyka; V V Urzhuntseva; S V Shishkina, Role of intermolecular interactions in formation of mono- and diaminopyridine crystals: study from the energetic viewpoint, Structural Chemistry, 2021, 32 (1), 235-257, DOI: 10.1007/s11224-020-01625-6
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Y Vaksler; A Idrissi; V V Urzhuntseva; S V Shishkina, Quantum Chemical Modeling of Mechanical Properties of Aspirin Polymorphic Modifications, Crystal Growth and Design, 2021, 21 (4), 2176-2186, DOI: 10.1021/acs.cgd.0c01613
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Maryna O Mazur; Oleksii S Zhelavskyi; Eugene M Zviagin; Svitlana V Shishkina; Vladimir I Musatov; Maksim A Kolosov; Elena H Shvets; Anna Yu Andryushchenko; Valentyn A Chebanov, Effective microwave-assisted approach to 1,2,3-triazolobenzodiazepinones via tandem Ugi reaction/catalyst-free intramolecular azide–alkyne cycloaddition, Beilstein Journal of Organic Chemistry, 2021, 17, 678-687, DOI: 10.3762/bjoc.17.57
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V Medviediev; S Shishkina; A O Ribalka; J K Zarȩba; M Drozd; M Daszkiewicz, Revisiting 2-chloro-4-nitroaniline: Analysis of intricate supramolecular ordering of a triclinic polymorph featuring a high: Z value and strong second harmonic generation, CrystEngComm, 2020, 22 (30), 5073-5085, DOI: 10.1039/d0ce00582g
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S V Shishkina; I V Ukrainets; O V Vashchenko; N I Voloshchuk; P S Bondarenko; L A Petrushova; G Sim, Biological properties of two enantiomorphic forms of N-(2,6-dimethylphenyl)-4-hydroxy-2,2-dioxo-1H-2λ6,1-benzothiazine-3-carboxamide, a structural analogue of piroxicam, Acta Crystallographica Section C: Structural Chemistry, 2020, 76, 69-74, DOI: 10.1107/S2053229619016450
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S V Shishkina; I S Konovalova; V R Karpina; S S Kovalenko; S M Kovalenko; N D Bunyatyan, Concomitant polymorphic forms of 3-cyclopropyl-5-(2-hydrazinylpyridin-3-yl)-1,2,4-oxadiazole, Acta Crystallographica Section C: Structural Chemistry, 2020, 76, 836-844, DOI: 10.1107/S2053229620010414
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I V Ukrainets; L A Petrushova; A I Fedosov; N I Voloshchuk; P S Bondarenko; S V Shishkina; L V Sidorenko; G Sim, Crystal habits and biological properties of N-(4-trifluoromethylphenyl)-4-hydroxy-2, 2-dioxo-1H-2λ6,1-benzothiazine-3-carboxamide, Scientia Pharmaceutica, 2020, 88 (1), DOI: 10.3390/scipharm88010001
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R D Oparin; Y A Vaksler; M A Krestyaninov; A Idrissi; S V Shishkina; M G Kiselev, Polymorphism and conformations of mefenamic acid in supercritical carbon dioxide, Journal of Supercritical Fluids, 2019, 152, DOI: 10.1016/j.supflu.2019.104547
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S V Shishkina, Using of quantum-chemical calculations to molecular crystals studying, Structural Chemistry, 2019, 30 (5), 1565-1577, DOI: 10.1007/s11224-019-01397-8
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I V Omelchenko; O V Shishkin; P Dopieralski; Z Latajka, About the Aromaticity of symm-Triaminotrinitrobenzene, Journal of Physical Chemistry A, 2019, 123 (11), 2244-2251, DOI: 10.1021/acs.jpca.9b00433
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S V Shishkina; I A Isaiev; V V Urzhuntseva; V A Palchykov, The formation of the salt and neutral molecule cocrystal from equimolar solution of heliamine and bicyclo[2.2.1]hept-5-ene-endo-2,3-dicarboxylic acid, Acta Crystallographica Section B: Structural Science, Crystal Engineering and Materials, 2019, 75 (2), 192-200, DOI: 10.1107/S205252061900115X
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I S Konovalova; S V Shishkina; G Bani-Khaled; E N Muzyka; A N Boyko, Intermolecular interactions in crystals of benzene and its mono- and dinitro derivatives: Study from the energetic viewpoint, CrystEngComm, 2019, 21 (18), 2908-2919, DOI: 10.1039/c8ce02099j
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O A Zhikol; S V Shishkina; V V Lipson; A N Semenenko; A V Mazepa; A V Borisov; P V Mateychenko, Low molecular weight supramolecular dehydroepiandrosterone-based gelators: Synthesis and molecular modeling study, New Journal of Chemistry, 2019, 43 (33), 13112-13121, DOI: 10.1039/c9nj01390c
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S V Shishkina; V N Baumer; O V Khromileva; L I Kucherenko; I A Mazur, The formation of two thiotriazoline polymorphs: Study from the energetic viewpoint, CrystEngComm, 2017, 19 (17), 2394-2401, DOI: 10.1039/c7ce00117g
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A N Puzan; V N Baumer; P V Mateychenko, Structure and decomposition of the silver formate Ag(HCO2), Journal of Solid State Chemistry, 2017, 246, 264-268, DOI: 10.1016/j.jssc.2016.11.022
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A N Puzan; V N Baumer; V V Vashchenko; D S Sofronov, Polymorphism of anhydrous cadmium oxalate CdC2O4, Journal of Alloys and Compounds, 2017, 726, 751-757, DOI: 10.1016/j.jallcom.2017.08.047
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S V Shishkina; I S Konovalova; O V Shishkin; A N Boyko, Influence of substituents on the acceptor properties of the amino groups in the diaminobenzene analogues, CrystEngComm, 2017, 19 (47), 7162-7176, DOI: 10.1039/c7ce01732d
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S V Shishkina; I S Konovalova; O V Shishkin; A N Boyko, Acceptor properties of amino groups in aminobenzene crystals: Study from the energetic viewpoint, CrystEngComm, 2017, 19 (42), 6274-6288, DOI: 10.1039/c7ce01382e
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I V Omelchenko; O V Shishkin, Basis set effects on the structure of isomeric nitroanilines: The role of basis set expansion, additional diffuse and polarization functions within the frame of DFT and MP2 approaches, Functional Materials, 2017, 24 (2), 270-277, DOI: 10.15407/fm24.02.270
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I V Ukrainets; S V Shishkina; V N Baumer; O V Gorokhova; L A Petrushova; G Sim, Two pseudo-enantiomeric forms of N-benzyl-4-hydroxy-1-methyl-2,2-dioxo-1H-2λ6,1-benzothiazine-3-carboxamide and their analgesic properties, Acta Crystallographica Section C: Structural Chemistry, 2016, 72 (5), 411-415, DOI: 10.1107/S2053229616005453
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A V Luzanov; O A Zhikol, Excited state structural analysis (ESSA) for correlated states of spin-flip type: Application to electronic excitations in nanodiamonds with defects, Functional Materials, 2016, 23 (1), 63-70, DOI: 10.15407/fm23.01.063
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S V Shishkina; O V Shishkin; V V Medviediev; I V Omelchenko; A I Ismiev; A M Magerramov, Weak but strong: Role of weak C-H···X (X=O, N) hydrogen bonds in organization of crystals of (1S,2S,3S,4R,5R,8S)-diethyl 2,4-dicyano-3-(furan-2-yl)-8-morpholino-6-oxobicyclo[3.2.1]octane-2,4-dicarboxylate, Structural Chemistry, 2016, 27 (1), 315-321, DOI: 10.1007/s11224-015-0698-1
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I V Omelchenko; O V Shishkin; L Gorb; J Leszczynski, Aromaticity and conformational flexibility of five-membered monoheterocycles: Pyrrole-like and thiophene-like structures, Structural Chemistry, 2016, 27 (1), 101-109, DOI: 10.1007/s11224-015-0707-4
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D S Yufit; O V Shishkin; R I Zubatyuk; J A K Howard, Trimethyltrioxane (paraldehyde) and its halomethanes complexes: Crystallization, structures, and analysis of packing motifs, Crystal Growth and Design, 2014, 14 (9), 4303-4309, DOI: 10.1021/cg500354t
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D S Yufit; O V Shishkin; R I Zubatyuk; J A K Howard, Low-melting molecular complexes. Part 5. Co-crystals of tetrahydrofuran and diethyl ether with methyl halides, Zeitschrift fur Kristallographie - Crystalline Materials, 2014, 229 (9), 639-647, DOI: 10.1515/zkri-2013-1718
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O V Shishkin; R I Zubatyuk; S V Shishkina; V V Dyakonenko; V V Medviediev, Role of supramolecular synthons in the formation of the supramolecular architecture of molecular crystals revisited from an energetic viewpoint, Physical Chemistry Chemical Physics, 2014, 16 (14), 6773-6786, DOI: 10.1039/c3cp55390f
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O V Shishkin; R I Zubatyuk; A V Maleev; R Boese, Investigation of topology of intermolecular interactions in the benzene-acetylene co-crystal by different theoretical methods, Structural Chemistry, 2014, 25 (5), 1547-1552, DOI: 10.1007/s11224-014-0413-7
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O V Shishkin; R I Zubatyuk; S M Desenko; J Leszczynski, A theoretical investigation of the relative stability of isomeric dihydropyridines, Chemistry of Heterocyclic Compounds, 2014, 50 (3), 327-335, DOI: 10.1007/s10593-014-1480-9
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O V Shishkin; P Dopieralski; I V Omelchenko; L Gorb; Z Latajka; J Leszczynski, Entropy versus aromaticity in the conformational dynamics of aromatic rings, Journal of Molecular Modeling, 2013, 19 (10), 4073-4077, DOI: 10.1007/s00894-012-1670-2
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S V Shishkina; A I Slabko; S Berski; Z Latajka; O V Shishkin, Tuning of character of the N-O bond in HONO from covalent to protocovalent by different types of intramolecular interactions, Journal of Chemical Physics, 2013, 139 (12), DOI: 10.1063/1.4821999
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O V Shishkin; I S Konovalova; R I Zubatyuk; G V Palamarchuk; S V Shishkina; A V Biitseva; I V Rudenko; V A Tkachuk; M Y Kornilov; O V Hordiyenko; J Leszczynski, Remarkably strong polarization of amidine fragment in the crystals of 1-imino-1H-isoindol-3-amine, Structural Chemistry, 2013, 24 (4), 1089-1097, DOI: 10.1007/s11224-012-0131-y
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S V Shishkina; A I Slabko; O V Shishkin, Conjugation vs hyperconjugation in molecular structure of acrolein, Chemical Physics Letters, 2013, 556, 18-22, DOI: 10.1016/j.cplett.2012.11.032
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O V Shishkin; V V Medvediev; R I Zubatyuk, Supramolecular architecture of molecular crystals possessing shearing mechanical properties: Columns versus layers, CrystEngComm, 2013, 15 (1), 160-167, DOI: 10.1039/c2ce26126j
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O V Shishkin; S V Shishkina; A V Maleev; R I Zubatyuk; V Vasylyeva; K Merz, Influence of deuteration and fluorination on the supramolecular architecture of pyridine N-oxide crystals, ChemPhysChem, 2013, 14 (4), 847-856, DOI: 10.1002/cphc.201200581
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I V Omelchenko; O V Shishkin; L Gorb; F C Hill; J Leszczynski, Substituent effects and aromaticity of six-membered heterocycles, Structural Chemistry, 2013, 24 (2), 725-733, DOI: 10.1007/s11224-012-0124-x
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I V Omelchenko; O V Shishkin; L Gorb; F C Hill; J Leszczynski, Properties, aromaticity, and substituents effects in poly nitro-and amino-substituted benzenes, Structural Chemistry, 2012, 23 (5), 1585-1597, DOI: 10.1007/s11224-012-9971-8
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O V Shishkin; V V Medvediev; R I Zubatyuk; O O Shyshkina; N V Kovalenko; J M Volovenko, Role of different molecular fragments in formation of the supramolecular architecture of the crystal of 1,1-dioxo-tetrahydro-1λ6- thiopyran-3-one, CrystEngComm, 2012, 14 (24), 8698-8707, DOI: 10.1039/c2ce26332g
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O V Shishkin; V V Dyakonenko; A V Maleev, Supramolecular architecture of crystals of fused hydrocarbons based on topology of intermolecular interactions, CrystEngComm, 2012, 14 (5), 1795-1804, DOI: 10.1039/c2ce06336k
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V Vasylyeva; O V Shishkin; A V Maleev; K Merz, Crystal structures of fluorinated pyridines from geometrical and energetic perspectives, Crystal Growth and Design, 2012, 12 (2), 1032-1039, DOI: 10.1021/cg201623e
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D S Yufit; R Zubatyuk; O V Shishkin; J A K Howard, Low-melting molecular complexes. Halogen bonds in molecular complexes of bromoform, CrystEngComm, 2012, 14 (23), 8222-8227, DOI: 10.1039/c2ce26191j
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O A Zhikol; O V Shishkin, Estimating stacking interaction energy using atom in molecules properties: Homodimers of benzene and pyridine, International Journal of Quantum Chemistry, 2012, 112 (18), 3008-3017, DOI: 10.1002/qua.24189
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O V Shishkin; P Dopieralski; I V Omelchenko; L Gorb; Z Latajka; J Leszczynski, Dynamical nonplanarity of benzene. Evidences from the Car-Parrinello molecular dynamics study, Journal of Physical Chemistry Letters, 2011, 2 (22), 2881-2884, DOI: 10.1021/jz201327t
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O V Shishkin; R I Zubatyuk; V V Dyakonenko; C Lepetit; R Chauvin, The C-Cl⋯π interactions inside supramolecular nanotubes of hexaethynylhexamethoxy[6]pericyclyne, Physical Chemistry Chemical Physics, 2011, 13 (15), 6837-6848, DOI: 10.1039/c0cp02666b
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I V Omelchenko; O V Shishkin; L Gorb; J Leszczynski; S Fias; P Bultinck, Aromaticity in heterocyclic analogues of benzene: Comprehensive analysis of structural aspects, electron delocalization and magnetic characteristics, Physical Chemistry Chemical Physics, 2011, 13 (46), 20536-20548, DOI: 10.1039/c1cp20905a
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O V Shishkin; I V Omelchenko; A L Kalyuzhny; B V Paponov, Intramolecular S···O chalcogen bond in thioindirubin, Structural Chemistry, 2010, 21 (5), 1005-1011, DOI: 10.1007/s11224-010-9638-2
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O V Shishkin; L Gorb; J Leszczynski, Conformational flexibility of pyrimidine ring in nucleic acid bases, Practical Aspects of Computational Chemistry: Methods, Concepts and Applications, 2010, 399-413, DOI: 10.1007/978-90-481-2687-3_21
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O V Shishkin; L Gorb; J Leszczynski, Conformational flexibility of pyrimidine rings of nucleic acid bases in polar environment: PCM study, Structural Chemistry, 2009, 20 (4), 743-749, DOI: 10.1007/s11224-009-9477-1
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D Schollmeyer; O V Shishkin; T Rühl; M O Vysotsky, OH-π and halogen-π interactions as driving forces in the crystal organisations of tri-bromo and tri-iodo trityl alcohols, CrystEngComm, 2008, 10 (6), 715-723, DOI: 10.1039/b716442d
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O V Shishkin, Evaluation of true energy of halogen bonding in the crystals of halogen derivatives of trityl alcohol, Chemical Physics Letters, 2008, 458 (1-3), 96-100, DOI: 10.1016/j.cplett.2008.04.106
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O V Shishkin; G V Palamarchuk; L Gorb; J Leszczynski, Opposite charges assisted extra strong C-H⋯O hydrogen bond in protonated 2′-deoxyadenosine monophosphate, Chemical Physics Letters, 2008, 452 (1-3), 198-205, DOI: 10.1016/j.cplett.2007.12.052
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R I Zubatyuk; Y M Volovenko; O V Shishkin; L Gorb; J Leszczynski, Aromaticity-controlled tautomerism and resonance-assisted hydrogen bonding in heterocyclic enaminone-iminoenol systems, Journal of Organic Chemistry, 2007, 72 (3), 725-735, DOI: 10.1021/jo0616411
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O V Shishkin; I V Omelchenko; M V Krasovska; R I Zubatyuk; L Gorb; J Leszczynski, Aromaticity of monosubstituted derivatives of benzene. The application of out-of-plane ring deformation energy for a quantitative description of aromaticity, Journal of Molecular Structure, 2006, 791 (1-3), 158-164, DOI: 10.1016/j.molstruc.2006.01.019
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M V Zhigalko; O V Shishkin, Conformational flexibility and aromaticity of azanaphthalenes, Journal of Structural Chemistry, 2006, 47 (5), 823-830, DOI: 10.1007/s10947-006-0397-2
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O V Shishkin; G V Palamarchuk; L Gorb; J Leszczynski, Intramolecular hydrogen bonds in canonical 2′-deoxyribonucleotides: An atoms in molecules study, Journal of Physical Chemistry B, 2006, 110 (9), 4413-4422, DOI: 10.1021/jp056902+
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O A Zhikol; O V Shishkin; K A Lyssenko; J Leszczynski, Electron density distribution in stacked benzene dimers: A new approach towards the estimation of stacking interaction energies, Journal of Chemical Physics, 2005, 122 (14), DOI: 10.1063/1.1877092
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O V Shishkin; L Gorb; O A Zhikol; J Leszczynski, Conformational analysis of canonical 2-deoxyribonucleotides. 1. Pyrimidine nucleotides, Journal of Biomolecular Structure and Dynamics, 2004, 21 (4), 537-553, DOI: 10.1080/07391102.2004.10506947
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O V Shishkin; L Gorb; O A Zhikol; J Leszczynski, Conformational analysis of canonical 2-deoxyribonucleotides. 2. Purine nucleotides, Journal of Biomolecular Structure and Dynamics, 2004, 22 (2), 227-243, DOI: 10.1080/07391102.2004.10506998
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O S Sukhanov; O V Shishkin; L Gorb; Y Podolyan; J Leszczynski, Molecular structure and hydrogen bonding in polyhydrated complexes of adenine: A DFT study, Journal of Physical Chemistry B, 2003, 107 (12), 2846-2852, DOI: 10.1021/jp026487a
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O V Shishkin; L Gorb; A V Luzanov; M Elstner; S Suhai; J Leszczynski, Structure and conformational flexibility of uracil: A comprehensive study of performance of the MP2, B3LYP and SCC-DFTB methods, Journal of Molecular Structure: THEOCHEM, 2003, 625 (1-3), 295-303, DOI: 10.1016/S0166-1280(03)00032-0
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O V Shishkin; K Y Pichugin; L Gorb; J Leszczynski, Structural non-rigidity of six-membered aromatic rings, Journal of Molecular Structure, 2002, 616 (1-3), 159-166, DOI: 10.1016/S0022-2860(02)00328-9
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S V Shishkina; O V Shishkin; J Leszczynski, Three-stage character of ring inversion in cyclohexene, Chemical Physics Letters, 2002, 354 (5-6), 428-434, DOI: 10.1016/S0009-2614(02)00156-2
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O V Shishkin, Conformational flexibility of 1,3-cyclohexadiene and its aza analogs, Journal of Structural Chemistry, 2000, 41 (3), 383-387, DOI: 10.1007/BF02741995
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O V Shishkin; A Pelmenschikov; D M Hovorun; J Leszczynski, Theoretical analysis of low-lying vibrational modes of free canonical 2-deoxyribonucleosides, Chemical Physics, 2000, 260 (3), 317-325, DOI: 10.1016/S0301-0104(00)00251-2
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O V Shishkin; L Gorb; J Leszczynski, Conformational flexibility of pyrimidine ring in adenine and related compounds, Chemical Physics Letters, 2000, 330 (5-6), 603-611, DOI: 10.1016/S0009-2614(00)01127-1
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O V Shishkin; L Gorb; P Hobza; J Leszczynski, Structural nonrigidity of nucleic acid bases. Post-Hartree-Fock ab initio study, International Journal of Quantum Chemistry, 2000, 80 (4-5), 1116-1124, DOI: 10.1002/1097-461x(2000)80:4/5<1116::aid-qua61>3.0.co;2-o