Cargando…
Mutual Relations between Substituent Effect, Hydrogen Bonding, and Aromaticity in Adenine-Uracil and Adenine-Adenine Base Pairs †
The electronic structure of substituted molecules is governed, to a significant extent, by the substituent effect (SE). In this paper, SEs in selected nucleic acid base pairs (Watson-Crick, Hoogsteen, adenine-adenine) are analyzed, with special emphasis on their influence on intramolecular interacti...
Autores principales: | Wieczorkiewicz, Paweł A., Szatylowicz, Halina, Krygowski, Tadeusz M. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7464026/ https://www.ncbi.nlm.nih.gov/pubmed/32823565 http://dx.doi.org/10.3390/molecules25163688 |
Ejemplares similares
-
Substituted adenine quartets: interplay between substituent effect, hydrogen bonding, and aromaticity
por: Szatylowicz, Halina, et al.
Publicado: (2020) -
Effect of the Solvent and Substituent on Tautomeric
Preferences of Amine-Adenine Tautomers
por: Jezuita, Anna, et al.
Publicado: (2021) -
Substituent effects on the stability of the four most stable tautomers of adenine and purine
por: Szatylowicz, Halina, et al.
Publicado: (2019) -
Impact of the Substituents
on the Electronic Structure of the Four Most Stable
Tautomers of Purine and Their Adenine Analogues
por: Jezuita, Anna, et al.
Publicado: (2020) -
Substituent Effect
versus Aromaticity—A Curious
Case of Fulvene Derivatives
por: Wieczorkiewicz, Pawel A., et al.
Publicado: (2023)