Multiwavelength-controlled multicolor photochromism and fluorescence switching based on an efficient photocyclization reaction by introducing two photoactive subunits into AIEgens
Abstract:Photochromic materials have recently attracted much attention in optoelectronic devices and optical storage systems because of their excellent reversible photoresponse performance. However, most traditional photochromic molecular systems have the limitation...
“…To overcome this problem, our group employed a new synthesis method to design a group of similar compounds in which two photochromic groups are located in cis conformation. 148 Introduction of two photoactive units greatly suppresses the AIE feature of these compounds, and significantly promotes their photochromic behaviours (Fig. 22).…”
Section: Solid-state Fluorescent Photoswitches Based On Diarylethenesmentioning
Photochromic materials have been widely used in data encryption, biological imaging, anti-counterfeiting, and other fields because of their excellent contrast, responsiveness, and fatigue resistance. However, materials that use fluorescence as...
“…To overcome this problem, our group employed a new synthesis method to design a group of similar compounds in which two photochromic groups are located in cis conformation. 148 Introduction of two photoactive units greatly suppresses the AIE feature of these compounds, and significantly promotes their photochromic behaviours (Fig. 22).…”
Section: Solid-state Fluorescent Photoswitches Based On Diarylethenesmentioning
Photochromic materials have been widely used in data encryption, biological imaging, anti-counterfeiting, and other fields because of their excellent contrast, responsiveness, and fatigue resistance. However, materials that use fluorescence as...
“…14–16 Among the various external stimuli, light is an ideal source with a high spatial and temporal resolution, clean, easy access, and simple operation. 17 Functional materials can spontaneously undergo structural transformations between at least two conformations through light-induced reversible or irreversible photochemical reactions with changes in physical properties such as viscosity, 18–20 shape, 21–24 fluorescence intensity, and colour 25–28 when irradiated by the light of a specific wavelength.…”
Section: Introductionmentioning
confidence: 99%
“…[14][15][16] Among the various external stimuli, light is an ideal source with a high spatial and temporal resolution, clean, easy access, and simple operation. 17 Functional materials can spontaneously undergo structural transformations between at least two conformations through light-induced reversible or irreversible photochemical reactions with changes in physical properties such as viscosity, [18][19][20] shape, [21][22][23][24] fluorescence intensity, and colour [25][26][27][28] when irradiated by the light of a specific wavelength. Among all response signals, fluorescent signals are increasingly gaining popularity in the research of light-stimulated responsive materials due to their designability, high sensitivity, and instantaneous visual feedback.…”
The development of light responsive fluorescent materials with nondestructive and high-contrast signaling properties has attracted much attention due to their potential use in a variety of areas, such as optical...
“…However, when one phenyl group of tetraphenylethene is replaced by a photoactive thienyl subunit, a reversible photochromism behaviour can effectively take place for the luminogen as reported in our previous paper [45] . Differing from reversible photochromism of tetraarylethene containing dual thienyl subgroups with high efficiency, [46] the cooperation of introduced thienyl subunit and pyridyl subunit in tetraarylethene surprisingly achieves irreversible fluorescence photoactivation with very high efficiency in a very short time of UV irradiation. The molecule designed luminogen (Z)‐4‐(1,2‐double‐(4‐4‐methoxyphenyl) ‐2‐ (thiophene‐3‐group) vinyl) pyridine (BMPTP) shows transient solid‐state emission behaviour, and then undergoes highly efficient photocyclization‐dehydrogenation reaction with a conversion rate of nearly 100 %.…”
Herein, we propose a rational design strategy by introducing photoactive thienyl and pyridyl groups into an AIE-active tetraarylethene skeleton to achieve highly efficient photochemistry-activated fluorescence enhancement from dominantly photo-physical aggregation-induced emission behavior, and prove that such photoactivated fluorescence enhancement is perfectly suited for superstable photocontrollable dual-mode patterning applications in both solution and solid matrix. It is found that the photoactivated fluorescence of designed AIEgen is attributed to the irreversible cyclized-dehydrogenation reaction under UV irradiation, and the oxidation product has a brighter fluorescence in both solution and solid states owning to its rigid and planar structure. The overall transformation rate of the AIEgen from its opened form to dehydrogenated form is up to nearly 100 % in a short period of UV irradiation, and the fast transformation and the stable product of this photochemical reaction guarantees super stability of photocontrolled patterning, which can be applied in photoactivated dual-mode patterning and advanced anti-counterfeiting.
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