Developing coordination complexes (such as metal-organic frameworks, MOFs) with circularly polarized luminescence (CPL) is currently attracting tremendous attention and remains a significant challenge in achieving MOF with circularly polarized afterglow. Herein, MOFs-based circularly polarized afterglow is first reported by combining the chiral induction approach and tuning the afterglow times by using the auxiliary ligands regulation strategy. The obtained chiral R/S-ZnIDC, R/S-ZnIDC(bpy), and R/S-ZnIDC(bpe)(IDC = 1H-Imidazole-4,5-dicarboxylate, bpy = 4,4'-Bipyridine, bpe = trans-1,2-Bis(4-pyridyl) ethylene) containing a similar structure unit display different afterglow times with 3, 1, and <0.1 s respectively which attribute to that the longer auxiliary ligand hinders the energy transfer through the hydrogen bonding. The obtained chiral complexes reveal a strong chiral signal, obvious photoluminescence afterglow feature, and strong CPL performance (g up to 3.7 × 10). Furthermore, the photo-curing 3D printing method is first proposed to prepare various chiral MOFs based monoliths from 2D patterns to 3D scaffolds for anti-counterfeiting and information encryption applications. This work not only develops chiral complexes monoliths by photo-curing 3D printing technique but opens a new strategy to achieve tunable CPL afterglow in optical applications.
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http://dx.doi.org/10.1002/adma.202313749 | DOI Listing |
J Am Chem Soc
January 2025
Department of Chemistry and Biomolecular Sciences, University of Ottawa, Ottawa, Ontario K1N 6N5, Canada.
The magnetic and magneto-optical properties of a tetrazinyl radical-bridged Er metallocene, [(Cp*Er)(bpytz)][BPh] (; Cp* = pentamethylcyclopentadienyl, bpytz = 3,6-bis(3,5-dimethyl-pyrazolyl)-1,2,4,5-tetrazine), are reported. As confirmed by these studies strong Ln-rad coupling is achieved, with exhibiting slow magnetic relaxation under a 1000 Oe dc field. The optical and magneto-optical profile of is completed by both near-infrared (NIR) luminescence and magnetic circularly polarized luminescence (MCPL), representing the first example of NIR MCPL with Er.
View Article and Find Full Text PDFNat Commun
January 2025
Key Laboratory for Photochemistry, Institute of Chemistry, Chinese Academy of Sciences, Beijing, China.
The preparation of single-crystal polymers with circularly polarized luminesce (CPL) remains a challenging task in chemistry and materials science. Herein, we present the single-crystal-to-single-crystal topochemical photopolymerization of a chiral organic salt to achieve this goal. The in-situ reaction of 1,4-bis((E)-2-(pyridin-4-yl)vinyl)benzene (1) with chiral (+)- or (-)-camphorsulfonic acid (CSA) gives the monomer crystal 1[( + )/( - )-CSA] showing yellow CPL with a high luminescent dissymmetry factor |g| of 0.
View Article and Find Full Text PDFLight Sci Appl
January 2025
Department of Material Science and Engineering, Pohang University of Science and Technology (POSTECH), Pohang, Republic of Korea.
Achiral dielectric nanostructures provide an efficient method for discriminating left- and right-circularly polarized photons, leveraging the photothermoelectric effect.
View Article and Find Full Text PDFACS Appl Opt Mater
December 2024
School of Materials Science and Engineering, Georgia Institute of Technology, Atlanta, Georgia 30332-0245, United States.
In this work, twisted helical cellulose nanocrystals films with preprogrammed circular polarization and near-infrared reflectance are fabricated via a blade-based 3D printing method. The films are composed of stacked nanoscale slabs with high birefringence from unidirectionally organized cellulose nanocrystals. By changing the printing director, we achieved two types of films: twisted helical stacks and anisotropic Bragg stacks.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
January 2025
Institute of Chemistry, CAS, Laboratory of Colloid and Interface Scie, Zhong Guancun, 100080, Beijing, CHINA.
Here, we report the synthesis and self-assembly of a novel chiral 2,3:6,7‒naphthalenediimide-based triangular macrocycle (NDI-∆) and their chiroptical properties. The enantiomeric NDI-∆ is synthesized by condensation of (RR) or (SS)-trans-1,2-cyclohexanediamine and 2,3,6,7-naphthalenetetracarboxylic 2,3:6,7-dianhydride, in which the chirality of the macrocycles is controlled by the diamine. With the rigid outer π-surface, the macrocycle showed unique chiroptical properties and self-assembly modes.
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