Abstract
Fluorescent photoswitches are highly attractive, because they hold great promises for photonic devices and imaging. However, a limited number of reversible switches with a response to light have been achieved in the solid state. Here, we report reversible dual fluorescent photoswitching characteristics in the solid state of spiropyran (SP)-functionalized tetraphenylethene (TPE) derivatives. These photoswitches exhibit two distinct and selectively addressable states, a cyan fluorescence and a red fluorescence, which can be conveyed into each other in a reversible feature upon irradiation with alternating UV and visible light. Detailed spectroscopic and theoretical studies suggest that the nonplanar molecular conformation of TPE moieties leads to large free volumes, which facilitates the reversible photoisomerization of SP. The excellent reversibility and high-contrast fluorescence of solid-state photoswitches enable great applications in multimodality anticounterfeiting and optical writing and erasing fluorescent devices.
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