Publications by authors named "Nuo-Hua Xie"

The magical fantasy of decades-old transformer characters is becoming closer to scientific reality, as transformable materials can change their shapes in response to thermal, mechanical, electrical, and chemical stimuli. However, precise and prompt control of plastic shaping remains to be wanted. Photoresponsive materials provide a promising alternative for rapid optomechanical shaping with limited success.

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A near-infrared fluorescence-switchable molecule, dithienylethene-terrylenediimide (TDI-4DTE) exhibits high near-infrared fluorescence and on/off ratio, decent reversibility, and fatigue resistance upon alternating UV/vis (305/621 nm) irradiation. Photoinduced electron transfer mainly contributes to the fluorescence quenching of TDI-4DTE. As an information storage unit, single molecular TDI-4DTE in the polymer film can be written by red light (621 nm) and erased by UV light (305 nm), while nondestructive fluorescence readout (750 nm) of a single molecular memory has been obtained upon excitation with near-infrared light (720 nm).

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A new photoswitchable near-infrared fluorophore (TDI-4DTE) with a symmetric structure exhibited reversible photo-controllable self-assembly and disassembly. The modification of π-conjugated terrylenediimide with four dithienylethene groups not only induced photoswitchable near-infrared fluorescence, but also photoregulated reversible precipitation-dissolution with microscopic and macroscopic polymorphism. Upon 302 nm UV-light irradiation, a noticeable precipitation was observed within seconds.

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Article Synopsis
  • Developed a new photoswitchable fluorophore called PEG-PMI-DTE that is both amphiphilic and resistant to fatigue.
  • The fluorophore allows for significant changes in fluorescence and shows bistable photochromism.
  • It can be used to visualize small liposome structures under super-resolution fluorescent microscopy with a high optical resolution of 30 nm.
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Monodisperse AIE (aggregation-induced emission)-active conjugated polymer nanoparticles are synthesized by dispersion polymerization using geminal Suzuki cross-coupling of 1,1-dibromoolefins. The size of the nanoparticles can be adjusted by varying the concentration of the initial monomer.

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We design and synthesize terrylenediimide-tetraphenylethene dyads, which exhibit featured aggregation-induced near-infrared fluorescence with a maximum emission wavelength of up to 800 nm.

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