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Crystalline and porous 2D poly(arylene vinylene)s (2D PAVs), vinylene-linked 2D conjugated covalent organic frameworks, represent promising materials for electronic and electrochemical applications. Chemically robust 2D PAVs with strong electron affinity are highly desirable for effective host-guest charge transfer to achieve enhanced device performance. Herein, we report the efficient synthesis and host-guest interaction of two novel 2D PAVs incorporating electron-deficient bipyrazine units with a N-free 2D PAV as a reference. They are crystalline and chemically robust. Various spectroscopies coupled with theoretical calculations indicate that the abundant N sites boost the electron affinity of 2D PAVs. We test their efficiency in hosting guest sulfur species and find that the electron-deficient materials help to physically confine and stabilize sulfur/polysulfide (, LiS) molecules with facilitated intermolecular charge transfer in the porous channels. As a result, using sulfur encapsulated by 2D PAVs as electrode materials, we achieve high specific capacities with excellent capacity retention after 200 charge-discharge cycles for Li-sulfur batteries.
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http://dx.doi.org/10.1039/d4sc06903j | DOI Listing |
J Phys Chem A
September 2025
Institute of Physics, Faculty of Physics, Astronomy, and Informatics, Nicolaus Copernicus University in Toruń, ul. Grudzia̧dzka 5, 87-100 Toruń, Poland.
A virtually no-cost method is proposed that can compute the correlation energies of general, covalently bonded, organic, and inorganic molecules (including conjugated π-electron systems) with a well-defined dominant Lewis structure at the accuracy of 99.5% of the near-exact values determined by the coupled-cluster singles, doubles, and perturbative triples [CCSD(T)] in the complete-basis-set (CBS) limit. This Correlation Energy Per Bond (CEPB) method assigns a partial correlation energy to each bond type (characterized by the identities of the two atoms forming the bond and its integer bond order) and to a lone pair, regardless of the bond length, bond angle, sp-hybridization, π-electron conjugation, ionicity, noncovalent interactions, etc.
View Article and Find Full Text PDFJ Am Chem Soc
September 2025
Frontiers Science Center for New Organic Matter, State Key Laboratory of Medicinal Chemical Biology, College of Life Sciences and Academy for Advanced Interdisciplinary Studies, Nankai University, Tianjin 300071, PR China.
Antigen-capturing nanomaterials hold great promise for cancer immunotherapy; however, the need for tumor localized administration and limited antigen-binding affinity remains the "Achilles heel" of this strategy. Herein, we present a tumor microenvironment (TME)-activatable nanoplatform, TDR848@FPB, designed for systemic administration and enhanced covalent capture of tumor-associated antigens (TAAs), enabling effective immunotherapy with minimal off-target effects and independent of localized tumor administration. This platform encapsulates a photosensitizer-conjugated, light-activated toll-like receptor (TLR) agonist, which induces immunogenic cell death and triggers a pro-inflammatory TME conducive to antigen capture upon light irradiation.
View Article and Find Full Text PDFSmall
September 2025
College of Chemistry, Chemical Engineering and Materials Science, Collaborative Innovation Center of Functionalized Probes for Chemical Imaging in Universities of Shandong, Key Laboratory of Molecular and Nano Probes, Ministry of Education, Shandong Normal University, Jinan, 250014, P. R. China.
The functionality of covalent organic frameworks (COFs) is usually highly related to their morphologies. Among various morphologies, the hollow-structured COFs have recently attracted intense attention due to their unique properties. Herein, the synthesis of hollow structured COFs are first reported with the chiral internal sites via combining the chiral templating method with the acid etching approach.
View Article and Find Full Text PDFAnal Chem
September 2025
Department of Chemistry, Wuhan University, Wuhan 430072, China.
Three-dimensional printing (3DP) technology enables the flexible fabrication of integrated monolithic microextraction chips for high-throughput sample pretreatment. Meanwhile, the extraction performance of 3DP-based channels is largely limited by printer resolution and the commercially available printing materials. In this work, a 3DP array monolithic microextraction chip (AMC) was fabricated by integrating 26-array helical monolithic microextraction channels for sample pretreatment and 52-array gas valves for fluid control.
View Article and Find Full Text PDFNatl Sci Rev
September 2025
Beijing Key Laboratory for Science and Application of Functional Molecular and Crystalline Materials, Department of Chemistry, University of Science and Technology Beijing, Beijing 100083, China.
Covalent organic frameworks (COFs) have great potential as versatile platforms for proton conduction. However, the commonly applied 2D COFs that are easy to design and synthesize have only 1D channels for proton conduction, limiting the formation of continuous hydrogen bonds due to the anisotropy between their crystalline grains. Herein, we report a strategy to construct 3D channels in 2D COFs by using rotaxane structures and eliminate the strong interlayer π-π interactions, facilitating the formation of smooth 3D proton-transfer pathways during guest doping.
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