Piotr Cysewski, Professor of Chemistry, D.Sc., Ph.D.

PAPERS

   

Curriculum Vitae

2019

  • Maciej Przybyłek, Tomasz Jeliński, Piotr Cysewski.  Application of multivariate adaptive regression splines (MARSplines) for predicting Hansen solubility parameters based on 1D and 2D molecular descriptors computed from SMILES string. J. Chem.  2019 : Vol. 2019, s. 1-15.
  • Maciej Przybyłek, Ł. Recki, K. Mroczyńska, Tomasz Jeliński, Piotr Cysewski. Experimental and theoretical solubility advantage screening of bi-component solid curcumin formulations. J. Drug Deliv. Sci. Technol. 2019 : Vol. 50, s. 125-135.
  • Piotr Cysewski. Application of the consonance solvent concept for accurate prediction of buckminster solubility in 180 net solvents using COSMO-RS approach. Symmetry-Basel 2019 : Vol. 11, nr 6, s. 1-20, 828
  • Tomasz Jeliński, Maciej Przybyłek, Piotr Cysewski. Natural deep eutectic solvents as agents for improving solubility, stability and delivery of curcumin. Pharm. Res.-DORDR 2019 : Vol. 36, 116, s. 1-10.
  • Piotr Cysewski, Maciej Przybyłek. Predicting value of binding constants of organic ligands to beta-cyclodextrin: application of MARSplines and descriptors encoded in SMILES string. Symmetry-Basel 2019 : Vol. 11, nr 7, s. 922; 1-11.
  • Piotr Cysewski. Prediction of ethenzamide solubility in organic solvents by explicit inclusions of intermolecular interactions within the framework of COSMO-RS-DARE. J. Mol. Liq. 2019
  • Tomasz Jeliński, Maciej Przybyłek, Piotr Cysewski. Solubility advantage of sulfanilamide and sulfacetamide in natural deep eutectic systems : experimental and theoretical investigations. Drug Dev. Ind. Pharm. 2019 : Vol. 45, nr 7, s. 1120-1129.
  • Beata Szefler, Przemysław Czeleń, Adam Szczepanik, Piotr Cysewski, Does Affinity of Cisplatin to B-Vitamins Impair the Therapeutic Effect in the Case of Patient with Lung Cancer Consuming Carrot or Beet Juice?, Anti-Cancer Agents in Medicinal Chemistry, 2019, 19, 000-000, DOI: 10.2174/1871520619666190325150624

2018

  • Maciej Przybyłek, Piotr Cysewski.Distinguishing cocrystals from simple eutectic mixtures : phenolic acids as potential pharmaceutical coformers.Cryst. Growth Des.2018 : Vol. 18, nr 6, s. 3524-3534.
  • Piotr Cysewski.Intermolecular interaction as a direct measure of water solubility advantage of meloxicam cocrystalized with carboxylic acids.J. Mol. Model.2018 : Vol. 24, nr 5, s. 112, 1-13.
  • Przemysław Krawczyk, Przemysław Czeleń, Piotr Cysewski.Reactive group effects on the photophysical and biological properties of 2-phenyl-1H-phenanthro[9,10-d]imidazole derivatives as fluorescent markers.Org. Biomol. Chem.2018 : Vol. 16, nr 20, s. 3788-3800.

2017

  • Maciej Przybyłek, D. Ziółkowska, K. Mroczyńska, Piotr Cysewski. Applicability of phenolic acids as effective enhancers of cocrystal solubility of methylxanthines.Cryst. Growth Des.2017 : Vol. 17, nr 4, s. 2186-2193.
  • Piotr Cysewski.In silico screening of dicarboxylic acids for cocrystallization with phenylpiperazine derivatives based on both cocrystallization propensity and solubility advantage.J. Mol. Model.2017 : Vol. 23, nr 4, s. 136, 1-11.
  • Tomasz Jeliński, Piotr Cysewski.Screening of ionic liquids for efficient extraction of methylxanthines using COSMO-RS methodology.Chem. Eng. Res. Des.2017 : Vol. 122, s. 176-183.
  • Piotr Cysewski, Maciej Przybyłek.Selection of effective cocrystals former for dissolution rate improvement of active pharmaceutical ingredients based on lipoaffinity index.Eur. J. Pharm. Sci.2017 : Vol. 107, s. 87-96.
  • Przemysław Krawczyk, B. Jędrzejewska, Piotr Cysewski, T. Janek.Synthesis, photophysical and biological properties of a new oxazolone fluorescent probe for bioimaging : an experimental and theoretical study.Org. Biomol. Chem.2017 : Vol. 15, nr 42, s. 8952-8966.
  • Przemysław Krawczyk, Przemysław Czeleń, Beata Szefler, Tomasz Jeliński, Piotr Cysewski.The reactive group effects on the photophysical and biological properties of the fluorescent probe based on chalcone derivatives.Modeling Interactions in Biomolecules VIII.J. Burda.Praha : MATFYZPRESS, Publishing House of the Faculty of Mathematics and Physics Charles University in Prague, 2017s. 74.: Plzeń, 2017.09.03
  • Przemysław Krawczyk, Przemysław Czeleń, Beata Szefler, Piotr Cysewski.Theoretical studies on the interaction between chalcone dyes and Concanavalin A - the reactive group effects on the photophysical and biological properties of the fluorescence probe.J. Photochem. Photobiol. A-Chem.2017 : Vol. 346, s. 327-337.
  • Beata Szefler, Przemysław Czeleń, Przemysław Krawczyk, Piotr Cysewski.Theoretical study on cisplatin binding to B-vitamins : could the therapeutic effect of cisplatin be decreased if a patient with lung cancer drinks carrot or beet juice?Modeling Interactions in Biomolecules VIII.J. Burda.Praha : MATFYZPRESS, Publishing House of the Faculty of Mathematics and Physics Charles University in Prague, 2017: Plzeń, 2017.09.03

2016

  • P. Cysewski, Efficacy of bi-component cocrystals and simple binary eutectics screening using heat of mixing estimated under super cooled conditions. J. Mol. Graph. Model. 2016, 68, 23-28
  • P. Cysewski, Transferability of cocrystallization propensities between aromatic and heteroaromatic amides. Struct. Chem. 2016, 27, 1403-1412
  • M. Przybyłek, D. Ziółkowska, K. Mroczyńska, P. Cysewski, Propensity of salicylamide and ethenzamide cocrystallization with aromatic carboxylic acids.Eur. J. Pharm. Sci. 2016, 85, 132-140
  • T. Jeliński, P. Cysewski, Structure and properties of alizarin complex formed with alkali metal hydroxides in methanol solution.J. Mol. Model. 2016, 22(6), 1-10.
  • T. Jeliński, P. Cysewski, The improvement of ecological characteristics of coatings from cured epoxy resins by hot water extractionJournal of Coatings Technology and Research, 2016, 13(6), 1047–1053
  • A. Markowska, P. Cysewski, L. Zając-Lamparska, Dowody uzasadniające wykorzystanie biofeedback HRV jako metody wspomagającej proces leczenia pacjentów mających problemy emocjonalne i objawy psychiatryczne.Pielęg. Zdr. Publ. 2016, 6(3), 221-228
  • P. Krawczyk, M. Pietrzak, T. Janek, B. Jędrzejewska, P. Cysewski, Spectroscopic and nonlinear optical properties of new chalcone fluorescent probes for bioimaging applications: a theoretical and experimental study, J. Mol. Model. 22 (2016) 1–11. doi:10.1007/s00894-016-2990-4
  • P. Cysewski, M. Przybyłek, D. Ziółkowska, K. Mroczyńska, Exploring the cocrystallization potential of urea and benzamide, J. Mol. Model. 22 (2016) 103. doi:10.1007/s00894-016-2964-6
  • M. Przybyłek, D. Ziółkowska, M. Kobierski, K. Mroczyńska, P. Cysewski, Utilization of oriented crystal growth for screening of aromatic carboxylic acids cocrystallization with urea, J. Cryst. Growth. 433 (2016) 128–138. doi:10.1016/j.jcrysgro.2015.10.015
  • I. Dziembowska, P. Izdebski, A. Rasmus, J. Brudny, M. Grzelczak, P. Cysewski, Effects of Heart Rate Variability Biofeedback on EEG Alpha Asymmetry and Anxiety Symptoms in Male Athletes: A Pilot Study., Appl. Psychophysiol. Biofeedback. 41 (2016) 141–50. doi:10.1007/s10484-015-9319-4
  • T. Jeliński, P. Cysewski, Structure and properties of alizarin complex formed with alkali metal hydroxides in methanol solution, J. Mol. Model. 22 (2016) 1–10. doi:10.1007/s00894-016-2988-y
  • P. Cysewski, Transferability of cocrystallization propensities between aromatic and heteroaromatic amides, Struct. Chem. (2016),1-10. doi:10.1007/s11224-016-0760-7
  • M. Przybyłek, D. Ziółkowska, K. Mroczyńska, P. Cysewski, Propensity of salicylamide and ethenzamide cocrystallization with aromatic carboxylic acids, Eur. J. Pharm. Sci. 85 (2016) 132–140. doi:10.1016/j.ejps.2016.02.010
  • T. Jeliński, P. Cysewski, E. Makarewicz, The control and optimization of the curing process of epoxy coatings: a case of poly (glycidoxy siloxane) resins, J. Polym. Eng. (2016). doi:10.1515/polyeng-2015-0276
  • P. Cysewski, Heat of formation distributions of components involved in bi-component cocrystals and simple binary eutectic mixtures, New J. Chem. 40 (2016) 187–194. doi:10.1039/C5NJ02013A

2015

  • P. Cysewski, M. Przybyłek, T. Miernik, M. Kobierski, D. Ziółkowska, On the origin of surfaces-dependent growth of benzoic acid crystal inferred through the droplet evaporation method, Struct. Chem. 26 (2015) 705–712. doi:10.1007/s11224-014-0528-x
  • M. Przybyłek, P. Cysewski, M. Pawelec, D. Ziółkowska, M. Kobierski, On the origin of surface imposed anisotropic growth of salicylic and acetylsalicylic acids crystals during droplet evaporation, J. Mol. Model. 21 (2015) 1–12. doi: 10.1007/s00894-015-2599-z
  • P. Cysewski, Pressure-imposed changes of benzoic acid crystals., J. Mol. Model. 21 (2015) 83. doi:10.1007/s00894-015-2635-z
  • E. Makarewicz, P. Cysewski, T. Jeliński, H. Maciejewski, I. Shyichuk, Study on properties of amine-cured glycidylsiloxane coatings, Przem. Chem. 94 (2015) 160–165. doi:10.15199/62.2015.2.5
  • P. Cysewski, R. Oliński, Structural, electronic and energetic consequences of epigenetic cytosine modifications, Phys. Chem. Chem. Phys. 17 (2015) 19616–19624. doi:10.1039/C5CP02188J

2014

  • T. Jeliński, P. Cysewski, Use of alizarin dye in spectrophotometric detection of residual amine in cured epoxy polymer, Przem. Chem. 93 (2014) 326–330. doi:dx.medra.org/10.12916/przemchem.2014.326
  • P. Cysewski, Apparent basicities of the surfaces characterizing the dominant crystal habits of distinct polymorphic forms of 4-aminosulfonamide, J. Mol. Model. 20 (2014). doi:10.1007/s00894-014-2276-7

2013

  • P. Czeleń, P. Cysewski, Structural and energetic properties of canonical and oxidized telomeric complexes studied by molecular dynamics simulations, J. Mol. Model. 19 (2013) 3339–3349. doi:10.1007/s00894-013-1859-z
  • P. Cysewski, T. Jeliński, Accuracy of color prediction of anthraquinone dyes in methanol solution estimated from first principle quantum chemistry computations., J. Mol. Model. 19 (2013) 4089–97. doi:10.1007/s00894-012-1717-4
  • P. Cysewski, Structural origin of apparent surface basicities of p-aminosulanamide polymorphs, Cryst. Res. Technol. 48(12) (2013) 1055-1065. doi:10.1002/crat.201300197
  • B. Jedrzejewska, P. Krawczyk, M. Pietrzak, M. Gordel, K. Matczyszyn, M. Samoć, et al., Styryl dye possessing donor-π-acceptor structure--Synthesis, spectroscopic and computational studies, Dye. Pigment. 99 (2013) 673–685. doi:10.1016/j.dyepig.2013.06.008
  • E. Makarewicz, P. Cysewski, A. Michalik, D. Ziółkowska, Properties of acid or alkali treated cadmium pigments, Dye. Pigment. 96 (2013) 338–348. doi:10.1016/j.dyepig.2012.08.004
  • T. Jeliński, P. Cysewski, E. Makarewicz, Application of alizarin colorimetric measurements for quantification of amine extraction by model food simulants from epoxy polymer, Springerplus. 2 (2013) 1–10. doi:10.1186/2193-1801-2-593
  • P. Cysewski, Application of Aromaticity Indices As Molecular Descriptors for Prediction of Optical Properties of 9,10-Anthraquinone Derivatives in Ethanol Solution, J. Theor. Comput. Chem. 12 (2013) 1350050. doi:10.1142/S0219633613500508

2012

  • P. Cysewski, T. Jeliński, T.M. Krygowski, W.P. Oziminski, Factors Influencing Aromaticity: PCA Studies of Monosubstituted Derivatives of Pentafulvene , Benzene and Heptafulvene, Chem, Curr Org. 16 (2012) 1920–1933. doi:10.2174/138527212802651205
  • P. Cysewski, T. Jeliński, M. Przybyłek, A. Shyichuk, Color prediction from first principle quantum chemistry computations: a case of alizarin dissolved in methanol, New J. Chem. 36 (2012) 1836–1843. doi:10.1039/c2nj40327g
  • P. Cysewski, B. Szefler, The pi-electron delocalization of phenol-fluoride system in explicit solvent conditions, Comput. Theor. Chem. 993 (2012) 97–105. doi:10.1016/j.comptc.2012.05.038

2011

  • P. Cysewski, Quantification of thermal ring flexibilities of aromatic and heteroaromatic compounds, J. Mol. Model., 2011: pp. 2249–2257. doi:10.1007/s00894-010-0901-7
  • P. Cysewski, Nonadditive Nature of Nucleobases Interactions in Model d(GpG) Dinucleotide Steps, Int. J. Quantum Chem. 111 (2011) 616–623. doi:10.1002/qua.22435
  • J. Gaca, G. Wejnerowska, P. Cysewski, Mechanism of the acidic hydrolysis of epichlorohydrin, J. Phys. Org. Chem. 24 (2011) 1045–1050. doi:10.1002/poc.1825
  • Michalik, D. Ziołkowska, P. Cysewski, E. Makarewicz, Effect of structure parameters of inorganic pigments on their adsorption properties, Przem. Chem. 90 (2011) 565–569
  • P. Cysewski, Influence of thermal vibrations on aromaticity of benzene, Phys. Chem. Chem. Phys. 13 (2011) 12998–13008. doi:10.1039/c1cp20165d
  • P. Cysewski, T. Jeliński, The pi-electron delocalization imposed by thermal vibrations of substituted benzene analogues in mediums of varying polarities, Comp. Method Sci. Tech. 17 (2011) 5–196. doi:10.12921/cmst.2011.17.01.05-16
  • D. Ziółkowska, A. Shyichuk, P. Cysewski, A. Organiściak, Flocculation efficiency of cationic potato starch in the presence of coagulants, Chemik. 65 (2011) 309–314
  • T. Jeliński, A. Shyichuk, D. Ziółkowska, Właściwości alkalizujące wybranych odpadów z produkcji sody metodą Solvay'a, Archiwum Gospodarki Odpadami i Ochrony Środowiska, vol. 13, 21-28, 2011.

2010

  • P. Cysewski, Non-additive interactions of nucleobases in model dinucleotide steps occurring in B-DNA crystals., in: J. Mol. Model., 2010: pp. 1721–1729. doi:10.1007/s00894-010-0722-8
  • P. Cysewski, P. Czeleń, Structural and energetic consequences of oxidation of d(ApGpGpGpTpT) telomere repeat unit in complex with TRF1 protein, in: J. Mol. Model., 2010: pp. 1797–1807. doi:10.1007/s00894-010-0730-8
  • P. Cysewski, B. Szefler, Environment influences on the aromatic character of nucleobases and amino acids., J. Mol. Model. 16 (2010) 1709–1720. doi:10.1007/s00894-010-0806-5
  • P. Cysewski, Molecular perspective review of biochemical role of nucleobases modified by oxidative stress, Comput. Meth. Sci. Technol. 16 (2010) 51–72.
  • Piotr Cysewski, W. Lasoń, Z. Sybilski, K. Lubiewska, P. Walecki, Edward Jacek Gorzelańczyk, Wpływ naświetlania światłem czerwonym i niebieskim na parametry grafomotoryczne oraz przewodność skóry - doniesienie wstępne, Episteme, 2010, 1(11), 127-142

2009

  • P. Cysewski, B. Szefler, H. Szatylowicz, T.M. Krygowski, An explicit solvent quantum chemistry study on the water environment influence on the interactions of fluoride with phenol, New J. Chem. 33 (2009) 831–837. doi:10.1039/b817297h
  • P. Cysewski, P. Czeleń, Structural and energetic heterogeneities of canonical and oxidized central guanine triad of B-DNA telomeric fragments., J. Mol. Model. 15 (2009) 607–613. doi:10.1007/s00894-008-0438-1
  • P. Cysewski, The post-SCF quantum chemistry characteristics of inter- and intra-strand stacking interactions in d(CpG) and d(GpC) steps found in B-DNA, A-DNA and Z-DNA crystals, in: J. Mol. Model., 2009: pp. 597–606. doi:10.1007/s00894-008-0378-9
  • P. Krawczyk, A. Kaczmarek, R. Zaleśny, K. Matczyszyn, W. Bartkowiak, M. Ziółkowski, P. Cysewski et al., Linear and nonlinear optical properties of azobenzene derivatives., J. Mol. Model. 15 (2009) 581–590. doi:10.1007/s00894-008-0436-3
  • P. Cysewski, K. Kozłowska, B. Szefler, Accurate micro- and macro- gas phase basicities of hydroxyl-radical-modified pyrimidines estimated by advanced quantum chemistry methods., J. Mol. Model. 15 (2009) 711–722. doi:10.1007/s00894-008-0423-8
  • P. Cysewski, Intra-strand stacking interactions in B-DNA crystals characterized by post-SCF quantum chemistry computations, New J. Chem. 33 (2009) 1909–1917. doi:10.1039/b909327c
  • P. Cysewski, B. Szefler, K. Kozłowska, Solvent impact on the aromaticity of benzene analogues: Implicit versus explicit solvent approach, in: J. Mol. Model., 2009: pp. 731–738. doi:10.1007/s00894-008-0440-7
  • P. Cysewski, Molecular origins of biological implications of DNA bases oxidation by reactive oxygen forms, Curr. Top. Biochem. Res. 11 (2009)
  • E. Makarewicz, M. Stempczyński, P. Cysewski, Investigations of dyeing of polyphasic water disperse systems using pigmental pastes, Chemik. 62 (2009) 14–21

2008

  • P. Cysewski, K. Kozłowska, Accurate Gas Phase Basicities of Hydroxyl Radical Modified Purines Estimated by Advanced Quantum Chemistry Methods, Pol. J. Chem. 82 (2008) 2255–2268. doi:10.12921/cmst.2010.16.01.51-72
  • P. Cysewski, Z. Czyżnikowska, R. Zaleśny, P. Czeleń, The post-SCF quantum chemistry characteristics of the guanine-guanine stacking B-DNA., Phys. Chem. Chem. Phys. 10 (2008) 2665–2672. doi:10.1039/b718635e
  • P. Cysewski, The post-SCF quantum chemistry characteristics of the energetic heterogeneity of stacked guanine-guanine pairs found in B-DNA and A-DNA crystals, J. Mol. Struct. THEOCHEM. 865 (2008) 36–43. doi:10.1016/j.theochem.2008.06.019
  • J. Nowaczyk, P. Olszowy, P. Cysewski, A. Nowaczyk, W. Czerwiński, Ozonization of electronic conducting polymers, Part III: The action of ozone on poly[3-pentylthiophene] film, Polym. Degrad. Stab. 93 (2008) 1275–1283. doi:10.1016/j.polymdegradstab.2008.04.005
  • P. Cysewski, A. Zalewska, E. Makarewicz, Application of regression methods to describing an emulsifying xylene in water with use of various surfactants, Przem. Chem. 87 (2008) 881–884
  • E. Makarewicz, J. Kowalik, P. Cysewski, Application of linear regression methods to describe emulsifying properties of fatty alcohol ethoxylate and fatty acid ethoxylate, Chemik. Vol. 61 (2008) 180–184
  • P. Cysewski, The impact of the nucleoside oxidation on the susceptibility to chemical carcinogens studied by first principle and semiempirical quantum chemistry methods, J. Mol. Struct. 863 (2008) 16–21. doi:10.1016/j.theochem.2008.05.004
  • Z. Czyżnikowska, R. Zaleśny, P. Cysewski, Quantum Chemical Study of the Nature of Stacking Interactions of 2-Oxo-adenine with Native B-DNA Purines, Pol. J. Chem. 82 (2008) 2269–2279
  • P. Cysewski, A post-SCF complete basis set study on the recognition patterns of uracil and cytosine by aromatic and pi-aromatic stacking interactions with amino acid residues., Phys. Chem. Chem. Phys. 10 (2008) 2636–2645. doi:10.1039/b718394a

2007

  • P. Cysewski, P. Czeleń, Theoretical analysis of the effects of guanine oxidative damage on the properties of B-DNA telomere fragments., J. Mol. Model. 13 (2007) 739–750. doi:10.1007/s00894-007-0186-7
  • P. Cysewski, Accurate gas phase acidities of carboxylic acids estimated by scaling the vibrational contribution of ab initio gibbs free energies, J. Mol. Model. 13 (2007) 801–808. doi:10.1007/s00894-007-0200-0
  • R. Zaleśny, K. Matczyszyn, A. Kaczmarek, W. Bartkowiak, P. Cysewski, Experimental and theoretical investigations of spectroscopic properties of azobenzene derivatives in solution., J. Mol. Model. 13 (2007) 785–791. doi:10.1007/s00894-007-0199-2
  • Ż. Czyżnikowska, R. Zaleśny, M. Ziółkowski, R.W. Góra, P. Cysewski, The nature of interactions in uracil dimer: An ab initio study, Chem. Phys. Lett. 450 (2007) 132–137. doi:10.1016/j.cplett.2007.10.106
  • P. Cysewski, P. Krol, A. Shyichuk, First principle simulations of ethylene glycol addition to diisocyanates, Macromol. Theory Simulations. 16 (2007) 541–547. doi:10.1002/mats.200700024
  • P. Cysewski, Z. Czyżnikowska-Balcerak, A Post-SCF quantum chemistry study on local minima of 8-oxo-guanine stacked with all four nucleic acid bases in B-DNA conformations, J. Heterocycl. Chem. 44 (2007) 765–773. doi:10.1002/jhet.5570440403

2006

  • P. Cysewski, A. Shyichuk, A first principle characterization of polyethylene, poly(propylene) and polystyrene macroradicals properties, Macromol. Theory Simulations. 15 (2006) 331–338. doi:10.1002/mats.200600001
  • P. Cysewski, Accurate gas phase acidities of carboxylic acids estimated by scaling of harmonic vibrational frequencies calculated on Hartree-Fock level, in: Recent Prog. Comput. Sci. Eng. Vols 7a 7b, 2006: pp. 1463–1468
  • P. Cysewski, A. Gackowska, J. Gaca, Experimental and theoretical studies on formation and degradation of chloro organic compounds., Chemosphere. 63 (2006) 165–170. doi:10.1016/j.chemosphere.2005.06.061

2005

  • P. Cysewski, An ab initio DFT characteristics of tautomeric properties of hydroxyl radical modified nucleosides in polar and non-polar environments, Zeitschrift Fur Phys. Chemie-International J. Res. Phys. Chem. Chem. Phys. 219 (2005) 213–234. doi:10.1524/zpch.219.2.213.57306
  • P. Cysewski, An ab initio study on nucleic acid bases aromaticities, J. Mol. Struct. THEOCHEM. 714 (2005) 29–34
  • Shyichuk, P. Cysewski, Polyolefin macroradical properties: A semiempirical quantum chemistry study, Macromol. Theory Simulations. 14 (2005) 400–405. doi:10.1002/mats.200500011
  • P. Cysewski, Ż. Czyżnikowska-Balcerak, The MP2 quantum chemistry study on the local minima of guanine stacked with all four nucleic acid bases in conformations corresponding to mean B-DNA, J. Mol. Struct. THEOCHEM. 757 (2005) 29–36. doi:10.1016/j.theochem.2005.06.014

2004

  • P. Cysewski, D. Bira, K. Białkowski, An ab initio quantum chemistry study on N-glycosidic bond stabilities of hydroxyl radical modified guanosine analogs, J. Mol. Struct. THEOCHEM. 678 (2004) 77–81. doi:10.1016/j.theochem.2004.03.010
  • P. Cysewski, B. Modzelewska-Banachiewicz, Quantum chemistry study on an intrinsic cis-trans equilibrium of 1,2,4-triazole-5-propenoic acid, Internet J. Chem. 7 (2004)
  • Shyichuk, D. Melnyk, P. Cysewski, Weakened bonds in polymer degradation intermediates as probable sites of macromolecular scission, Polimery. 49 (2004) 449–452

2003

  • P. Cysewski, Z. Czyżnikowska-Balcerak, B. Szefler, An ab initio post SCF study on stacking interactions of 8-oxo-9-methylguanine with four canonical DNA bases, Pol. J. Chem. 77 (2003) 1287–1300
  • P. Cysewski, D. Bednarek, K. Kozłowska, Proton affinities and N-glycosidic bond stabilities of hydroxyl radical modified adenosine, Phys. Chem. Chem. Phys. 5 (2003) 4899–4904. doi:10.1039/b307744f

2000

  • P. Cysewski, Ab initio calculations of the pairing of four canonical DNA bases with three thymine derivatives generated by hydroxyl radical in anaerobic conditions, Pol. J. Chem. 74 (2000) 245–256

1999

  • P. Cysewski, Structure and properties of hydroxyl radical modified nucleic acid components: pairing properties of 2-hydroxyadenine and 8-oxoadenine, J. Mol. Struct. 466 (1999) 59–67. doi:10.1016/S0166-1280(98)00341-8
  • P. Cysewski, Structure and properties of hydroxyl radical modified nucleic acid components: tautomerism and miscoding properties of 5-hydroxycytosine, J. Mol. Struct. 466 (1999) 49–58. doi:10.1016/S0166-1280(98)00337-6
  • P. Cysewski, Coding properties of thymine derivatives generated by hydroxyl radical in aerobic conditions, Phys. Chem. Chem. Phys. 1 (1999) 1531–1537. doi:10.1039/a808236g
  • P. Cysewski, D. Jeziorek, R. Oliński, Structure and tautomeric properties of cytosine derivatives generated by a hydroxyl radical in aerobic conditions, J. Mol. Struct. THEOCHEM. 459 (1999) 1–14. doi:10.1016/S0166-1280(98)00205-X
  • P. Cysewski, R. Oliński, Theoretical description of the coding potential of diamino-5-formamidopyrimidines, Zeitschrift Fur Naturforsch. - Sect. C J. Biosci. 54 (1999) 239–245. doi:10.1515/znc-1999-3-414
  • P. Cysewski, R. Oliński, Ab initio quantum chemistry studies on the coding properties of cytosine derivatives generated by hydroxyl radical in aerobic conditions, J. Mol. Struct. 490 (1999) 69–79. doi:10.1016/S0166-1280(99)00069-X
  • P. Cysewski, Structure and tautomeric properties of thymine derivatives generated by hydroxyl radical in anaerobic conditions, J. Mol. Struct. THEOCHEM. 467 (1999) 51–61. doi:10.1016/S0166-1280(98)00479-5

1998

  • P. Cysewski, Theoretical studies on the tautomeric properties of diamino-5-formamidopyrimidines, Zeitschrift Fur Naturforsch. C-a J. Biosci. 53 (1998) 1027–1036
  • P. Cysewski, An ab initio study of the tautomeric and coding properties of 8-oxo-guanine, J. Chem. Soc. Trans. 94 (1998) 3117–3125. doi:10.1039/a804512g
  • P. Cysewski, D. Jeziorek, R. Oliński, Structure and tautomeric properties of thymine derivatives generated by hydroxyl radical in aerobic conditions, J. Chem. Soc. Trans. 94 (1998) 1813–1821. doi:10.1039/a800546j
  • P. Cysewski, D. Jeziorek, An ab initio SCF study on the tautomerisation of the 8-oxo-guanine and xanthine, J. Mol. Struct. THEOCHEM. 430 (1998) 219–229. doi:10.1016/S0166-1280(98)90245-7

1997

  • P. Cysewski, C. VidalMadjar, R. Jordan, R. Oliński, Structure and properties of hydroxyl radical modified nucleic acid components .2. 8-oxo-adenine and 8-oxo-2’-deoxy-adenosine, Theochem-Journal Mol. Struct. 397 (1997) 167–177. doi:10.1016/S0166-1280(96)04994-9

1996

  • P. Cysewski, D. Jeziorek, R. Oliński, An ab initio SCF study on the tautomerisation of fapy-guanine, Theochem-Journal Mol. Struct. 369 (1996) 93–104. doi:10.1016/S0166-1280(96)04596-4
  • K. Białkowski, P. Cysewski, R. Olinski, Effect of 2’-deoxyguanosine oxidation at C8 position on N-glycosidic bond stability, Zeitschrift Fur Naturforsch. - Sect. C J. Biosci. 51 (1996) 119–122

1995

  • P. Cysewski, C. V Madjar, V. Noinville, R. Oliński, Structure and properties of 2-hydroxy-adenine and 2-hydroxy-2’-deoxy-adenosine, Bull. Soc. Chim. Fr. 132 (1995) 453–460
  • P. Cysewski, D. Jeziorek, R. Oliński, W. Woźnicki, Ab-initio studies on the structure and properties of the hydroxyl-radical-modified adenine-derivatives in different tautomeric forms, J. Phys. Chem. 99 (1995) 9702–9708. doi:10.1021/j100024a010

1993

  • E. Makarewicz, P. Cysewski, An attempt to describe the plastification of polyvinylchloride in terms of the theory of volume filling of micropores, Colloid Polym. Sci. 271 (1993) 236–240

1992

  • E. Makarewicz, P. Cysewski, An attempted description of the PVC plasticization process using the theory of volume filling of micropores, Int. Polym. Sci. Technol. 19 (1992) T–58
  • R. Lemque, A. Jaulmes, B. Sébille, C. Vidal-Madjar, P. Cysewski, Study of the adsorption of self-associating proteins on an anion exchanger: application to the chromatography of β-lactoglobulin B, J. Chromatogr. A. 599 (1992) 255–265. doi:10.1016/0021-9673(92)85478-C

1991

  • P. Cysewski, A. Jaulmes, R. Lemque, B. Sebille, C. Vidalmadjar, G. Jilge, Multivalent ion-exchange model of biopolymer chromatography for mass overload conditions, J. Chromatogr. 548 (1991) 61–79. doi:10.1016/S0021-9673(01)88592-7
  • J.K. Garbacz, P. Cysewski, A. Świątkowski, The idea of structural heterogeneity of an absorbent in the description of adsorption equilibrium in a system: solid-binary liquid non-electrolyte solution, Pol. J. Chem. 65 (1991) 479

1990

  • P. Cysewski, J.K. Garbacz, S. Biniak, Description of the energetical heterogeneity of adsorption systems: solid/liquid solution based on the adsorption of iodine from non-aqueous solutions on active carbon, Pol. J. Chem. 68 (1990) 305–313
  • J.K. Garbacz, P. Cysewski, S. Biniak, Opis adsorpcji fizycznej z ciekłych roztworó w dwuskładnikowych na powierzchniach ciał stałych w oparciu o analogi równań Freundlich i Dubinina-Raduszkiewicza, Zesz. Bydgoskiego Tow. Nauk. Ser. A. 18 (1990) 3–13
  • P. Cysewski, J.K. Garbacz, S. Biniak, A. Świątkowski, Description of the energetic heterogeneity of solid—liquid adsorption systems based on experimental isotherms of adsorption of iodine from non-aqueous solutions on microporous active carbons, Pol. J. Chem. 64 (1990) 267

1989

  • J.K. Garbacz, P. Cysewski, B. Rymian, S. Biniak, 3-parameter analogs of Freundlich and Ddubinin-Rradushkevich equations for the description of adsorption from 2-component liquid solutions of non-electrolytes on solids, Pol. J. Chem. 63 (1989) 205–213

1988

  • P. Cysewski, J.K. Garbacz, S. Biniak, Determination of the microporous adsorbents structure hetergogeneity in the proces of physical adsorption from two-component non-electrolyte solutions, Adsorpt. Sci. Technol. 5 (1988) 106–115
  • P. Cysewski, J.K. Garbacz, S. Biniak, A. Świątkowski, A. Dąbrowski, Description of isotherms of two-component non-electrolyte solution adsorption onto solids with structural heterogeneity of adsorbents taken into consideration, Adsorpt. Sci. Technol. 5 (1988) 106–115. doi:10.1177/026361748800500202

1987

  • J.K. Garbacz, S. Biniak, P. Cysewski, An attempt to apply of the Dubini-Radushkevich and Freundlich equatons for describing isotherms of adsorption from binary liquid solutions of non-electrolytes with unlimited miscibility, Adsorpt. Sci. Technol. 1-2 (1987) 105–111

1986

  • J.K. Garbacz, P. Cysewski, S. Biniak, A. Świątkowski, Adaptation of the Freundlich and Dubinin-Radushkevich equations to describe adsorption on microporous solids from binary non-electrolyte solutions with limited miscibility of the components, Adsorpt. Sci. Technol. 3 (1986) 253–260. doi:10.1177/026361748600300406