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ACS Omega|September 14, 2020
What Is the Main Feature Distinguishing the Through-Space Interactions in Cyclophanes from Their Aliphatic Analogues?Irena Majerz, Teresa DziembowskaThe Journal of Physical Chemistry. A|August 6, 2014
Substituents and environment influences on aromaticity of peri- and para-substituted naphthalenesIrena Majerz, Teresa DziembowskaMolecular Diversity|February 21, 2019
Substituent effect on inter-ring interaction in paracyclophanesIrena Majerz, Teresa DziembowskaActa Crystallographica Section B, Structural Science, Crystal Engineering and Materials|April 5, 2018
Aromaticity of benzene derivatives: an exploration of the Cambridge Structural DatabaseIrena Majerz, Teresa DziembowskaThe Journal of Physical Chemistry. A|May 25, 2012
Aromaticity of overcrowded nitroanilinesIrena Majerz, Teresa DziembowskaThe Journal of Physical Chemistry. A|March 11, 2017
Aromaticity of peri- and para-Substituted Naphthalene-1-carbaldehyde. Comparison with 1-NitronaphthaleneIrena Majerz, Teresa DziembowskaThe Journal of Physical Chemistry. A|October 1, 2016
Aromaticity and Through-Space Interaction between Aromatic Rings in [2.2]ParacyclophanesIrena Majerz, Teresa DziembowskaJournal of Computer-Aided Molecular Design|September 16, 2018
Weak interactions in furan dimersIrena MajerzOrganic & Biomolecular Chemistry|January 12, 2011
The influence of potassium cation on a strong OHO hydrogen bondIrena MajerzThe Journal of Physical Chemistry. A|July 11, 2012
Directionality of inter- and intramolecular OHO hydrogen bonds: DFT study followed by AIM and NBO analysisIrena MajerzPageof 4