Standard

Intramolecular hydrogen bonds in selected aromatic compounds: recent developments. / Jezierska, Aneta ; Tolstoy, Peter M. ; Panek, Jarosław J. ; Filarowski, Aleksander.

в: Catalysts, Том 9, № 11, 909, 11.2019.

Результаты исследований: Научные публикации в периодических изданияхОбзорная статьяРецензирование

Harvard

Jezierska, A, Tolstoy, PM, Panek, JJ & Filarowski, A 2019, 'Intramolecular hydrogen bonds in selected aromatic compounds: recent developments', Catalysts, Том. 9, № 11, 909. https://doi.org/10.3390/catal9110909

APA

Jezierska, A., Tolstoy, P. M., Panek, J. J., & Filarowski, A. (2019). Intramolecular hydrogen bonds in selected aromatic compounds: recent developments. Catalysts, 9(11), [909]. https://doi.org/10.3390/catal9110909

Vancouver

Jezierska A, Tolstoy PM, Panek JJ, Filarowski A. Intramolecular hydrogen bonds in selected aromatic compounds: recent developments. Catalysts. 2019 Нояб.;9(11). 909. https://doi.org/10.3390/catal9110909

Author

Jezierska, Aneta ; Tolstoy, Peter M. ; Panek, Jarosław J. ; Filarowski, Aleksander. / Intramolecular hydrogen bonds in selected aromatic compounds: recent developments. в: Catalysts. 2019 ; Том 9, № 11.

BibTeX

@article{cb41ff5d2b7c4e5cb6322b800191a854,
title = "Intramolecular hydrogen bonds in selected aromatic compounds: recent developments",
abstract = "A review of intramolecular hydrogen bonding in ortho-hydroxyaryl Schiff bases, ortho-hydroxyaryl Mannich bases, dipyrrins, ortho-hydroxyaryl ketones, ortho-hydroxyaryl amides, and 4-Bora-3a,4a-diaza-s-indacene (BODIPY) dyes with tautomeric sensors as substituents is presented in this paper. Ortho-hydroxy Schiff and Mannich base derivatives are known as model molecules for analysing the properties of intramolecular hydrogen bonding. The compounds under discussion possess physicochemical features modulated by the presence of strong intramolecular hydrogen bonds. The equilibrium between intra- and inter-molecular hydrogen bonds in BODIPY is discussed. Therefore, the summary can serve as a knowledge compendium of the influence of the hydrogen bond on the molecular properties of aromatic compounds.",
keywords = "Acetophenone, Amide, BODIPY, Cyclically arranged hydrogen bond, Schiff base",
author = "Aneta Jezierska and Tolstoy, {Peter M.} and Panek, {Jaros{\l}aw J.} and Aleksander Filarowski",
note = "Jezierska, A.; Tolstoy, P.M.; Panek, J.J.; Filarowski, A. Intramolecular Hydrogen Bonds in Selected Aromatic Compounds: Recent Developments. Catalysts 2019, 9, 909.",
year = "2019",
month = nov,
doi = "10.3390/catal9110909",
language = "English",
volume = "9",
journal = "Catalysts",
issn = "2073-4344",
publisher = "MDPI AG",
number = "11",

}

RIS

TY - JOUR

T1 - Intramolecular hydrogen bonds in selected aromatic compounds: recent developments

AU - Jezierska, Aneta

AU - Tolstoy, Peter M.

AU - Panek, Jarosław J.

AU - Filarowski, Aleksander

N1 - Jezierska, A.; Tolstoy, P.M.; Panek, J.J.; Filarowski, A. Intramolecular Hydrogen Bonds in Selected Aromatic Compounds: Recent Developments. Catalysts 2019, 9, 909.

PY - 2019/11

Y1 - 2019/11

N2 - A review of intramolecular hydrogen bonding in ortho-hydroxyaryl Schiff bases, ortho-hydroxyaryl Mannich bases, dipyrrins, ortho-hydroxyaryl ketones, ortho-hydroxyaryl amides, and 4-Bora-3a,4a-diaza-s-indacene (BODIPY) dyes with tautomeric sensors as substituents is presented in this paper. Ortho-hydroxy Schiff and Mannich base derivatives are known as model molecules for analysing the properties of intramolecular hydrogen bonding. The compounds under discussion possess physicochemical features modulated by the presence of strong intramolecular hydrogen bonds. The equilibrium between intra- and inter-molecular hydrogen bonds in BODIPY is discussed. Therefore, the summary can serve as a knowledge compendium of the influence of the hydrogen bond on the molecular properties of aromatic compounds.

AB - A review of intramolecular hydrogen bonding in ortho-hydroxyaryl Schiff bases, ortho-hydroxyaryl Mannich bases, dipyrrins, ortho-hydroxyaryl ketones, ortho-hydroxyaryl amides, and 4-Bora-3a,4a-diaza-s-indacene (BODIPY) dyes with tautomeric sensors as substituents is presented in this paper. Ortho-hydroxy Schiff and Mannich base derivatives are known as model molecules for analysing the properties of intramolecular hydrogen bonding. The compounds under discussion possess physicochemical features modulated by the presence of strong intramolecular hydrogen bonds. The equilibrium between intra- and inter-molecular hydrogen bonds in BODIPY is discussed. Therefore, the summary can serve as a knowledge compendium of the influence of the hydrogen bond on the molecular properties of aromatic compounds.

KW - Acetophenone

KW - Amide

KW - BODIPY

KW - Cyclically arranged hydrogen bond

KW - Schiff base

UR - http://www.scopus.com/inward/record.url?scp=85074391851&partnerID=8YFLogxK

U2 - 10.3390/catal9110909

DO - 10.3390/catal9110909

M3 - Review article

VL - 9

JO - Catalysts

JF - Catalysts

SN - 2073-4344

IS - 11

M1 - 909

ER -

ID: 48656630