We present herein an easy way to prepare novel responsive hydrogels by simply doping lanthanide complexes into a polymer hydrogel, poly(2-acrylamido-2-methyl-1-propanesulfonicacid) (PAMPSA). The resulting hybrid hydrogels can be readily processed into a range of shapes. Both the on-off luminescence switching and the healable properties are simultaneously achieved in the resulting responsive hybrid hydrogels. They exhibit effectively self-healing performance without any external stimulus and reversible "on-off" luminescence switching triggered by exposure to acid-base vapor. The key to this on-off luminescence switching behavior is that the protonation of the organic ligands compete with full coordination to Ln(3+) and that incomplete coordination affects the luminescence yield. The high proton strength in the resulting hydrogels makes the doped lanthanide complexes unstable, and ammonia (or triethylamine) vapor can dramatically decrease the proton strength through neutralization, driving the full coordination of the ligand to Ln(3+).
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http://dx.doi.org/10.1021/acs.langmuir.5b03102 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Physics and Optoelectronic Engineering, Ludong University, Yantai 264000, China.
Constructing multifunctional phosphors grounded in the intricate relationship between energy level structures and luminescent properties has captivated researchers in the luminescent material field. Herein, using the embedded cluster multiconfigurational ab initio method, the energy levels of Bi in the SrLaGaO host at different geometries were calculated, which results in the establishment of complete configurational coordinate curves, yielding breathing mode vibrational frequencies and equilibrium bond lengths for all excited states. These curves supply deep insight into the luminescence properties of Bi-doped phosphors and highlight the impact of ions in the second coordination sphere on luminescence.
View Article and Find Full Text PDFChemistry
January 2025
Beijing Normal University, College of Chemistry, Xiejiekou NO.19, 100875, Beijing, CHINA.
Optically pure monosubstituted [n]paracyclophanes are promising candidates for material synthesis, asymmetric catalysis, and drug discovery. Thus far, only a few catalytic asymmetric synthesis processes have been reported for assessing these stained atropisomers. In this study, we describe a highly enantioselective synthesis of monosubstituted [n]paracyclophanes by combining desymmetrization and kinetic resolution.
View Article and Find Full Text PDFMater Horiz
January 2025
Key Laboratory of Functional Inorganic Material Chemistry (MOE), School of Chemistry and Materials Science, Heilongjiang University, Harbin 150080, China.
In such an era of information explosion, improving the level of information security is still a challenging task. Self-erasing luminescent hydrogels are becoming ideal candidates for improving the level of information security with simple encryption and decryption methods. Herein, a lanthanide-polyoxometalate-based self-erasing luminescent hydrogel with time-dependent and resilient properties was constructed through a covalent crosslinked network constructed with polyacrylamide and a non-covalent crosslinked network constructed with [2-(methacryloyloxy)ethyl]trimethyl ammonium chloride/NaDyWO, along with doping urease.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Xiangtan University, College of Chemistry, CHINA.
Efficient circularly polarized luminescence (CPL) optical waveguides have significant potential for advancing photonic and optoelectronic devices. However, the development of CPL optical waveguides materials (OWMs) with low optical loss coefficient remains a considerable challenge. To overcome this, we design and synthesize CPL OWMs based on room-temperature phosphorescent liquid crystalline polymers (LCPs).
View Article and Find Full Text PDFJ Am Chem Soc
January 2025
School of Chemistry, Chemical Engineering and Biotechnology, Nanyang Technological University, 70 Nanyang Drive, Singapore 637457, Singapore.
Afterglow luminescence provides ultrasensitive optical detection by minimizing tissue autofluorescence and increasing the signal-to-noise ratio. However, due to the lack of suitable unimolecular afterglow scaffolds, current afterglow agents are nanocomposites containing multiple components with limited afterglow performance and have rarely been applied for cancer theranostics. Herein, we report the synthesis of a series of oxathiine-containing donor-acceptor block semiconducting polymers (PDCDs) and the observation of their high photoreactivity and strong near-infrared (NIR) afterglow luminescence.
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