The sequestration of luminophores within supramolecular polyhedral compartments of a crystalline zeolite-like hydrogen-bonded framework illustrates a unique approach to limiting the self-quenching ordinarily exhibited at the high concentrations achievable in this framework. A range of differently sized luminescent guests, namely coumarin 1, coumarin 4, fluorescein, [Ru(bpy) ]Cl , and rhodamine B, can be encapsulated in amounts of up to one molecule per cage, equivalent to a concentration of 0.175 m, which is significantly higher than the concentration at which aggregation-induced quenching occurs in other media. The luminescence spectra of the encapsulated guests are consistent with the presence of isolated monomers and the absence of self-quenching. The emission color of the single crystals can be tuned readily from blue to red through the choice of guest molecules. These observations promise an approach to organic solid-state lasing compounds if crystals of sufficient size and quality can be prepared.
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http://dx.doi.org/10.1002/anie.201707097 | DOI Listing |
Soft Matter
November 2024
Zhengzhou University, Zhengzhou 450000, P. R. China.
Circularly polarized luminescence (CPL) refers to the differentiation of the left-handed and right-handed emissions of chiral systems in the excited state. Serving as an alternative characterization method to circular dichroism (CD), CPL can detect changes in fluorescence in a chiral system, which could be more efficient in recognizing chiral species. Although CPL can be generated by attaching luminophores to a chiral unit through a covalent bond, the non-covalent bonding of fluorescent chromophores with chiral species or helical nanostructures can also induce CPL and their changes.
View Article and Find Full Text PDFAnal Chem
October 2024
Key Laboratory of Analytical Chemistry for Life Science of Shaanxi Province, School of Chemistry and Chemical Engineering, Shaanxi Normal University, Xi'an 710062, China.
Obtaining stable electrochemiluminescence (ECL) emissions from a hydrophobic luminophore in aqueous solutions and designing a method without the use of an exogenous coreactant are promising for ECL biosensing. Here, a highly sensitive signal-on ECL immunoassay for the SARS-CoV-2 N protein was developed using micelles as an ECL tag. The micelles were prepared by coencapsulating the luminophore hydrophobic CdSe/ZnS quantum dots and coreactant dibenzoyl peroxide within the hydrophobic core of micelles.
View Article and Find Full Text PDFSmall
December 2024
Key Laboratory of Colloid and Interface Chemistry of Ministry of Education, School of Chemistry and Chemical Engineering, Shandong University, Jinan, 250100, P. R. China.
Inherent luminescent short peptides essentially provide opportunities to rationally manipulate supramolecular chirality and chiral luminescence. Herein, a facile protocol to construct a series of naphthalimide-appended dipeptides is reported that show ultrasound wave-activated supramolecular chirality regulated by odd-even law. Naphthalimide luminophores are conjugated to the dipeptide skeleton with variable alkyl spacers.
View Article and Find Full Text PDFChemistry
October 2024
Faculty of Chemistry (Organic Chemistry), Center of Medical Biotechnology (ZMB) and Center for Nanointegration Duisburg-Essen (CENIDE), University of Duisburg-Essen, Universitätsstr. 7, 45117, Essen, Germany.
In this contribution we report on a novel approach towards luminescent light-responsive ligands. To this end, cyanostilbene- guanidiniocarbonyl-pyrrole hybrids were designed and investigated. Merging of a luminophore with a supramolecular bioactive ligand bears numerous advantages by overcoming the typical drawbacks of drug-labelling, influencing the overall performance of the active species by attachment of a large luminophore.
View Article and Find Full Text PDFNanoscale
July 2024
Departamento de Química Orgánica, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria, s/n, 28040-Madrid, Spain.
The synthesis of the [6]helicene-based luminophores 1 and 2 is reported. These chiral systems, endowed with cyano-stilbene fragments, form supramolecular polymers by the operation of intermolecular H-bonding interactions between the amides present in the peripheral side chains. The dissimilar disubstitution of 1 and 2 plays a crucial role in their self-assembling features.
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