Cargando…
Proton-Stabilized Photochemically Reversible E/Z Isomerization of Spiropyrans
[Image: see text] Spiropyrans undergo C(spiro)–O bond breaking to their ring-open protonated E-merocyanine form upon protonation and irradiation via an intermediate protonated Z-merocyanine isomer. We show that the extent of acid-induced ring opening is controlled by matching both the concentration...
Autores principales: | Kortekaas, L., Chen, J., Jacquemin, D., Browne, W. R. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2018
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6150689/ https://www.ncbi.nlm.nih.gov/pubmed/29847129 http://dx.doi.org/10.1021/acs.jpcb.8b03528 |
Ejemplares similares
-
Noncommutative Switching of Double Spiropyrans
por: Kortekaas, Luuk, et al.
Publicado: (2020) -
Electrochemical Ring-Opening and -Closing of a Spiropyran
por: Steen, Jorn D., et al.
Publicado: (2021) -
Spiropyran Meets Guanine Quadruplexes: Isomerization Mechanism and DNA Binding Modes of Quinolizidine‐Substituted Spiropyran Probes
por: Avagliano, Davide, et al.
Publicado: (2020) -
Polarity-Driven
Isomerization of a Hydroxynaphthalimide-Containing
Spiropyran at Room Temperature
por: Shiraishi, Yasuhiro, et al.
Publicado: (2023) -
Spontaneous Isomerization of a Hydroxynaphthalene-Containing
Spiropyran in Polar Solvents Enhanced by Hydrogen Bonding Interactions
por: Shiraishi, Yasuhiro, et al.
Publicado: (2021)