Tadeusz Marek Krygowski

According to our database1, Tadeusz Marek Krygowski authored at least 17 papers between 1993 and 2022.

Collaborative distances:
  • Dijkstra number2 of five.
  • Erdős number3 of five.

Timeline

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Bibliography

2022
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, 2022

2021
Solvent Effect on the Stability and Reverse Substituent Effect in Nitropurine Tautomers.
Symmetry, 2021

Dependence of the substituent energy on the level of theory.
J. Comput. Chem., 2021

2017
The role of the long-range exchange corrections in the description of electron delocalization in aromatic species.
J. Comput. Chem., 2017

2013
Complexes of 4-substituted phenolates with HF and HCN: Energy decomposition and electronic structure analyses of hydrogen bonding.
J. Comput. Chem., 2013

2010
How to Find the Fries Structures for Benzenoid Hydrocarbons.
Symmetry, 2010

2009
Are Thermodynamic and Kinetic Stabilities Correlated? A Topological Index of Reactivity toward Electrophiles Used as a Criterion of Aromaticity of Polycyclic Benzenoid Hydrocarbons.
J. Chem. Inf. Model., 2009

2008
Why Are the Kinked Polyacenes More Stable than the Straight Ones? A Topological Study and Introduction of a New Topological Index of Aromaticity.
J. Chem. Inf. Model., 2008

2007
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., 2007

2005
Theoretical Study of Changes in pi-Electron Delocalization in the Analogues of an <i>o</i><i>rtho</i>-Hydroxy Schiff Base When the Proton Is Replaced with Li<sup>+</sup> or BeH<sup>+</sup>.
J. Chem. Inf. Model., 2005

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., 2005

2004
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., 2004

1996
Separation of the Energetic and Geometric Contributions to Aromaticity, 2. Analysis of the Aromatic Character of Benzene Rings in Their Various Topological Environments in the Benzenoid Hydrocarbons. Crystal and Molecular Structure of Coronene.
J. Chem. Inf. Comput. Sci., 1996

Separation of the Energetic and Geometric Contributions to Aromaticity, 3. Analysis of the Aromatic Character of Benzene Rings in Their Various Topological and Chemical Environments in the Substituted Benzene Derivatives.
J. Chem. Inf. Comput. Sci., 1996

1995
Aromatic Character of the Benzene Ring Present in Various Topological Environments in Benzenoid Hydrocarbons. Nonequivalence of Indices of Aromaticity.
J. Chem. Inf. Comput. Sci., 1995

Local Aromatic Character of C60 and C70 and Their Derivatives.
J. Chem. Inf. Comput. Sci., 1995

1993
Crystallographic studies of inter- and intramolecular interactions reflected in aromatic character of .pi.-electron systems.
J. Chem. Inf. Comput. Sci., 1993


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