Your browser doesn't support javascript.
loading
Tailoring the optical and dynamic properties of iminothioindoxyl photoswitches through acidochromism.
Medved', Miroslav; Hoorens, Mark W H; Di Donato, Mariangela; Laurent, Adèle D; Fan, Jiayun; Taddei, Maria; Hilbers, Michiel; Feringa, Ben L; Buma, Wybren Jan; Szymanski, Wiktor.
Afiliación
  • Medved' M; Regional Centre of Advanced Technologies and Materials, Faculty of Science, Palacký University in Olomouc Slechtitelu 27 CZ-771 46 Olomouc Czech Republic miroslav.medved@umb.sk.
  • Hoorens MWH; Department of Chemistry, Faculty of Natural Sciences, Matej Bel University Tajovského 40 SK-97400 Banská Bystrica Slovak Republic.
  • Di Donato M; University Medical Center Groningen, Department of Radiology, Medical Imaging Center, University of Groningen Hanzeplein 1 9713 GZ Groningen The Netherlands w.szymanski@umcg.nl.
  • Laurent AD; Centre for Systems Chemistry, Stratingh Institute for Chemistry, Faculty of Science and Engineering, University of Groningen Nijenborgh 7 9747 AG Groningen The Netherlands.
  • Fan J; European Laboratory for Non Linear Spectroscopy (LENS) via N. Carrara 1 50019 Sesto Fiorentino Italy.
  • Taddei M; ICCOM-CNR via Madonna del Piano 10 50019 Sesto Fiorentino (FI) Italy.
  • Hilbers M; Laboratoire CEISAM UMR UN-CNRS 6230, Université de Nantes Nantes F-44000 France.
  • Feringa BL; Van't Hoff Institute for Molecular Sciences, University of Amsterdam Science Park 904 1098 XH Amsterdam The Netherlands.
  • Buma WJ; European Laboratory for Non Linear Spectroscopy (LENS) via N. Carrara 1 50019 Sesto Fiorentino Italy.
  • Szymanski W; Van't Hoff Institute for Molecular Sciences, University of Amsterdam Science Park 904 1098 XH Amsterdam The Netherlands.
Chem Sci ; 12(12): 4588-4598, 2021 Feb 09.
Article en En | MEDLINE | ID: mdl-34163724
Multi-responsive functional molecules are key for obtaining user-defined control of the properties and functions of chemical and biological systems. In this respect, pH-responsive photochromes, whose switching can be directed with light and acid-base equilibria, have emerged as highly attractive molecular units. The challenge in their design comes from the need to accommodate application-defined boundary conditions for both light- and protonation-responsivity. Here we combine time-resolved spectroscopic studies, on time scales ranging from femtoseconds to seconds, with density functional theory (DFT) calculations to elucidate and apply the acidochromism of a recently designed iminothioindoxyl (ITI) photoswitch. We show that protonation of the thermally stable Z isomer leads to a strong batochromically-shifted absorption band, allowing for fast isomerization to the metastable E isomer with light in the 500-600 nm region. Theoretical studies of the reaction mechanism reveal the crucial role of the acid-base equilibrium which controls the populations of the protonated and neutral forms of the E isomer. Since the former is thermally stable, while the latter re-isomerizes on a millisecond time scale, we are able to modulate the half-life of ITIs over three orders of magnitude by shifting this equilibrium. Finally, stable bidirectional switching of protonated ITI with green and red light is demonstrated with a half-life in the range of tens of seconds. Altogether, we designed a new type of multi-responsive molecular switch in which protonation red-shifts the activation wavelength by over 100 nm and enables efficient tuning of the half-life in the millisecond-second range.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Chem Sci Año: 2021 Tipo del documento: Article Pais de publicación: Reino Unido