Journal
ANALYTICAL CHEMISTRY
Volume 85, Issue 5, Pages 2983-2990Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ac4000283
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- Swiss National Science Foundation (SNF)
- Austrian Science Fund (FWF) [J3343]
- Austrian Science Fund (FWF) [J 3343] Funding Source: researchfish
- Austrian Science Fund (FWF) [J3343] Funding Source: Austrian Science Fund (FWF)
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Photoresponsive ion extraction/release systems (PRIONERS) represent a highly interesting tool for the localized and time-controlled chemical perturbation of biological materials. We report here on our first results on phototriggered calcium and sodium exchanging materials. Such materials exist in two distinct states (on and off), depending on the wavelength of illumination. We used a combination of spectroscopic and electrochemical methods to obtain a better understanding of the dynamic processes involved in the triggered ion-exchange reaction upon activation of the photoactive compound. The driving force for the ion exchange is the light-induced acidity change chromoionophore. Activation with UV light generates a species in the membrane with an increased pK(a). Protons are pulled into the membrane, and at the same time, ions are expelled. The selectivity of the system is determined by the employed ionophore. In contrast to photoresponsive ionophore-based systems, the concept presented here is applicable for virtually any ion of interest for which an ionophore exists.
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