| Aromaticity from the viewpoint of molecular geometry: application to planar systems TM Krygowski, H Szatylowicz, OA Stasyuk, J Dominikowska, M Palusiak Chemical reviews 114 (12), 6383-6422, 2014 | 511 | 2014 |
| The electron density of delocalized bonds (EDDB) applied for quantifying aromaticity DW Szczepanik, M Andrzejak, J Dominikowska, B Pawełek, ... Physical Chemistry Chemical Physics 19 (42), 28970-28981, 2017 | 146 | 2017 |
| Structural aspects of the intermolecular hydrogen bond strength: H‐bonded complexes of aniline, phenol and pyridine derivatives H Szatyłowicz Journal of Physical Organic Chemistry 21 (10), 897-914, 2008 | 109 | 2008 |
| The role of the long‐range exchange corrections in the description of electron delocalization in aromatic species DW Szczepanik, M Sola, M Andrzejak, B Pawełek, J Dominikowska, ... Journal of Computational Chemistry 38 (18), 1640-1654, 2017 | 81 | 2017 |
| Characterizing the strength of individual hydrogen bonds in DNA base pairs H Szatyłowicz, N Sadlej-Sosnowska Journal of chemical information and modeling 50 (12), 2151-2161, 2010 | 79 | 2010 |
| How H-bonding modifies molecular structure and π-electron delocalization in the ring of pyridine/pyridinium derivatives involved in H-bond complexation TM Krygowski, H Szatyłowicz, JE Zachara The Journal of organic chemistry 70 (22), 8859-8865, 2005 | 76 | 2005 |
| A tautomeric equilibrium between functionalized 2-formylphenylboronic acids and corresponding 1, 3-dihydro-1, 3-dihydroxybenzo [c][2, 1] oxaboroles S Luliński, I Madura, J Serwatowski, H Szatyłowicz, J Zachara New Journal of Chemistry 31 (1), 144-154, 2007 | 61 | 2007 |
| How amino and nitro substituents direct electrophilic aromatic substitution in benzene: an explanation with Kohn–Sham molecular orbital theory and Voronoi deformation density … OA Stasyuk, H Szatylowicz, TM Krygowski, CF Guerra Physical Chemistry Chemical Physics 18 (17), 11624-11633, 2016 | 60 | 2016 |
| Aromaticity: what does it mean? TM Krygowski, H Szatylowicz ChemTexts 1, 1-10, 2015 | 53 | 2015 |
| Molecular Geometry as a Source of Chemical Information. 3. How H-Bonding Affects Aromaticity of the Ring in the Case of Phenol and p-Nitrophenol Complexes … TM Krygowski, JE Zachara, H Szatylowicz The Journal of Organic Chemistry 69 (21), 7038-7043, 2004 | 53 | 2004 |
| Substituent effects of nitro group in cyclic compounds A Jezuita, K Ejsmont, H Szatylowicz Structural Chemistry 32 (1), 179-203, 2021 | 52 | 2021 |
| Towards physical interpretation of substituent effects: The case of meta-and para-substituted anilines H Szatylowicz, T Siodla, OA Stasyuk, TM Krygowski Physical Chemistry Chemical Physics 18 (17), 11711-11721, 2016 | 45 | 2016 |
| Theoretical study of electron-attracting ability of the nitro group: classical and reverse substituent effects OA Stasyuk, H Szatylowicz, C Fonseca Guerra, TM Krygowski Structural Chemistry 26, 905-913, 2015 | 45 | 2015 |
| How the Shape of the NH2 Group Depends on the Substituent Effect and H-Bond Formation in Derivatives of Aniline H Szatyłowicz, TM Krygowski, P Hobza The Journal of Physical Chemistry A 111 (1), 170-175, 2007 | 44 | 2007 |
| Aromaticity of acenes: the model of migrating π-circuits DW Szczepanik, M Sola, TM Krygowski, H Szatylowicz, M Andrzejak, ... Physical Chemistry Chemical Physics 20 (19), 13430-13436, 2018 | 42 | 2018 |
| Toward the physical interpretation of inductive and resonance substituent effects and reexamination based on quantum chemical modeling H Szatylowicz, A Jezuita, T Siodła, KS Varaksin, MA Domanski, K Ejsmont, ... ACS omega 2 (10), 7163-7171, 2017 | 36 | 2017 |
| H-Bonded Complexes of Aniline with HF/F− and Anilide with HF in Terms of Symmetry-Adapted Perturbation, Atoms in Molecules, and Natural Bond Orbitals Theories H Szatyłowicz, TM Krygowski, JJ Panek, A Jezierska The Journal of Physical Chemistry A 112 (40), 9895-9905, 2008 | 36 | 2008 |
| Effect of the H-bonding on aromaticity of purine tautomers OA Stasyuk, H Szatyłowicz, TM Krygowski The Journal of organic chemistry 77 (8), 4035-4045, 2012 | 35 | 2012 |
| How H-bonding affects aromaticity of the ring in variously substituted phenol complexes with bases. 4. Molecular geometry as a source of chemical information TM Krygowski, H Szatyłowicz, JE Zachara Journal of chemical information and computer sciences 44 (6), 2077-2082, 2004 | 35 | 2004 |
| Molecular geometry as a source of chemical information. Part 2—An attempt to estimate the H‐bond strength: the case of p‐nitrophenol complexes with bases TM Krygowski, JE Zachara, H Szatylowicz Journal of physical organic chemistry 18 (2), 110-114, 2005 | 34 | 2005 |
