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Cited article:

Strong intermolecular OH…N hydrogen bond as a source of polymorphism in the complex of pentachlorophenol with 4-methylpyridine

J. Janczak, J. Baran, H. Ratajczak and I. Majerz
Journal of Molecular Structure 1327 141234 (2025)
https://doi.org/10.1016/j.molstruc.2024.141234

1H-MAS-NMR Chemical Shifts in Hydrogen-Bonded Complexes of Chlorophenols (Pentachlorophenol, 2,4,6-Trichlorophenol, 2,6-Dichlorophenol, 3,5-Dichlorophenol, and p-Chlorophenol) and Amine, and H/D Isotope Effects on 1H-MAS-NMR Spectra

Hisashi Honda
Molecules 18 (4) 4786 (2013)
https://doi.org/10.3390/molecules18044786

Changes of electron density in the OHN hydrogen bond upon proton transfer in complexes of phenols with trimethylamine: DFT study

Emilia Kwiatkowska and Irena Majerz
Journal of Physical Organic Chemistry 21 (10) 867 (2008)
https://doi.org/10.1002/poc.1386

Strength from Weakness: Structural Consequences of Weak Interactions in Molecules, Supermolecules, and Crystals

Paola Gilli and Gastone Gilli
Strength from Weakness: Structural Consequences of Weak Interactions in Molecules, Supermolecules, and Crystals 261 (2002)
https://doi.org/10.1007/978-94-010-0546-3_14

Spectrophotometric determination of the transition system for interactions involving model hydrogen bonds in acetonitrile

Józef Magoński
Journal of Physical Organic Chemistry 15 (4) 204 (2002)
https://doi.org/10.1002/poc.466

The crystal structures at 80 K and IR spectra of the complex of 4-methylpyridine with pentachlorophenol and its deuterated analogue

Z. Malarski, I. Majerz and T. Lis
Journal of Molecular Structure 380 (3) 249 (1996)
https://doi.org/10.1016/0022-2860(96)09223-X

The crystal structures at 80 K and IR spectra of the complex of 4-methylpyridine with pentachlorophenol and its deuterated analogue

Z. Malarski, I. Majerz and T. Lis
Journal of Molecular Structure: THEOCHEM 380 (3) 249 (1996)
https://doi.org/10.1016/S0166-1280(96)90959-8