Cargando…
“Vermellogens” and the Development of CB[8]-Based Supramolecular Switches Using pH-Responsive and Non-Toxic Viologen Analogues
[Image: see text] We present herein the “vermellogens”, a new class of pH-responsive viologen analogues, which replace the direct linking between para-substituted pyridinium moieties within those by a hydrazone functional group. A series of such compounds have been efficiently synthesized in aqueous...
Autores principales: | Barravecchia, Liliana, Blanco-Gómez, Arturo, Neira, Iago, Skackauskaite, Raminta, Vila, Alejandro, Rey-Rico, Ana, Peinador, Carlos, García, Marcos D. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682480/ https://www.ncbi.nlm.nih.gov/pubmed/36206443 http://dx.doi.org/10.1021/jacs.2c08575 |
Ejemplares similares
-
Amino Acid–Viologen
Hybrids: Synthesis, Cucurbituril
Host–Guest Chemistry, and Implementation on the Production
of Peptides
por: Barravecchia, Liliana, et al.
Publicado: (2021) -
Thinking outside the “Blue Box”: from molecular to supramolecular pH-responsiveness
por: Blanco-Gómez, Arturo, et al.
Publicado: (2019) -
CB[7]- and CB[8]-Based [2]-(Pseudo)rotaxanes with
Triphenylphosphonium-Capped Threads: Serendipitous Discovery of a
New High-Affinity Binding Motif
por: Neira, Iago, et al.
Publicado: (2022) -
Reversible 2D Supramolecular Organic Frameworks encompassing Viologen Cation Radicals and CB[8]
por: Madasamy, Kanagaraj, et al.
Publicado: (2018) -
Chemical redox-induced chiroptical switching of supramolecular assemblies of viologens
por: Kuwahara, Yutaka, et al.
Publicado: (2022)