Yong Tian , Shun He , Liqi Wu , Kairong Zang , Fuhua Huang , Hong Wang , Jian Chen
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引用次数: 0
Abstract
Stimuli-responsive fluorescent polymeric nanoparticles have gained widespread interest in information encryption and anti-counterfeiting because of their features including easy preparation, high contrast, and good photostability. However, most of reported single-responsive nanoparticles exhibited the low security of information encryption and anti-counterfeiting, and limited their application. Therefore, we reported photo- and Al3+-responsive fluorescent polymeric nanoparticles (PAFPNs) through a simple one-pot miniemulsion polymerization. Based on fluorescence resonance energy transfer (FRET) mechanism, Al3+-responsive fluorescence groups ((E)-N′-(2-hydroxybenzylidene)-4-vinylbenzohydrazide (HBVBH)) and spiropyran-linked methacrylate (SPMA) were used to construct FRET systems. Initially, the nanoparticles showed no fluorescence. Upon the addition of Al3+ (100 μM), the PAFPNs revealed a strong blue fluorescence, due to the HBVBH can chelate with Al3+ to produce a blue fluorescence via a metal chelation-enhanced fluorescence mechanism (CHEF). Subsequently, UV can induce a photoisomerization process of SPMA from a non-fluorescent spiropyran (SP) state to a merocyanine (MC) form with red fluorescence, enabling a transition in fluorescence from blue to red. Finally, the PAFPNs can return to blue fluorescence via the irradiation of visible light. PAFPNs not only exhibited the three fluorescent states of no-blue-red, but also revealed high fluorescence contrast and outstanding photoreversibility. These results implied that PAFPNs have a great potential in developing multilevel information encryption, anti-counterfeiting, and multicolor security inks.
期刊介绍:
JPPA publishes the results of fundamental studies on all aspects of chemical phenomena induced by interactions between light and molecules/matter of all kinds.
All systems capable of being described at the molecular or integrated multimolecular level are appropriate for the journal. This includes all molecular chemical species as well as biomolecular, supramolecular, polymer and other macromolecular systems, as well as solid state photochemistry. In addition, the journal publishes studies of semiconductor and other photoactive organic and inorganic materials, photocatalysis (organic, inorganic, supramolecular and superconductor).
The scope includes condensed and gas phase photochemistry, as well as synchrotron radiation chemistry. A broad range of processes and techniques in photochemistry are covered such as light induced energy, electron and proton transfer; nonlinear photochemical behavior; mechanistic investigation of photochemical reactions and identification of the products of photochemical reactions; quantum yield determinations and measurements of rate constants for primary and secondary photochemical processes; steady-state and time-resolved emission, ultrafast spectroscopic methods, single molecule spectroscopy, time resolved X-ray diffraction, luminescence microscopy, and scattering spectroscopy applied to photochemistry. Papers in emerging and applied areas such as luminescent sensors, electroluminescence, solar energy conversion, atmospheric photochemistry, environmental remediation, and related photocatalytic chemistry are also welcome.