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Halina Szatylowicz
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2020 – today
- 2022
- [j8]Pawel Wieczorkiewicz
, Halina Szatylowicz
Energetic and Geometric Characteristics of Substituents, Part 3: The Case of NO2 and NH2 Groups in Their Mono-Substituted Derivatives of Six-Membered Heterocycles. Symmetry 14(1): 145 (2022) - 2021
- [j7]Anna Jezuita
Solvent Effect on the Stability and Reverse Substituent Effect in Nitropurine Tautomers. Symmetry 13(7): 1223 (2021)
2010 – 2019
- 2017
- [j6]Dariusz W. Szczepanik
The role of the long-range exchange corrections in the description of electron delocalization in aromatic species. J. Comput. Chem. 38(18): 1640-1654 (2017) - 2013
- [j5]Halina Szatylowicz
Complexes of 4-substituted phenolates with HF and HCN: Energy decomposition and electronic structure analyses of hydrogen bonding. J. Comput. Chem. 34(8): 696-705 (2013) - 2010
- [j4]Halina Szatylowicz
Characterizing the Strength of Individual Hydrogen Bonds in DNA Base Pairs. J. Chem. Inf. Model. 50(12): 2151-2161 (2010)
2000 – 2009
- 2007
- [j3]Halina Szatylowicz
Long-Distance Structural Consequences of H-Bonding. How H-Bonding Affects Aromaticity of the Ring in Variously Substituted Aniline/Anilinium/Anilide Complexes with Bases and Acids. J. Chem. Inf. Model. 47(3): 875-886 (2007) - 2005
- [j2]Tadeusz Marek Krygowski, Halina Szatylowicz
Molecular Geometry as a Source of Chemical Information. 5. Substituent Effect on Proton Transfer in Para-Substituted Phenol Complexes with Fluoride-a B3LYP/6-311+G** Study. J. Chem. Inf. Model. 45(3): 652-656 (2005) - 2004
- [j1]Tadeusz Marek Krygowski, Halina Szatylowicz
How H-Bonding Affects Aromaticity of the Ring in Variously Substituted Phenol Complexes with Bases. 4. Molecular Geometry as a Source of Chemical Information. J. Chem. Inf. Model. 44(6): 2077-2082 (2004)
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