ArticleAngewandte Chemie (International ed. in English)2025
Electronegative Strategic Positions in Covalent Organic Frameworks: Unlocking High-Efficiency Gold Recovery.
Article in Angewandte Chemie (International ed. in English), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
4 citing papers in PubMed.
- Light-Promoted Efficient Gold Recovery Enabled by a Polydopamine-Functionalized Covalent Organic Framework.Angewandte Chemie (International ed. in English) · 2026Article
- Local polarity modulation in triangular pores of covalent organic frameworks for iodine capture from water.Nature communications · 2026Article
- Electronegative Strategic Positions in Covalent Organic Frameworks: Unlocking High-Efficiency Gold Recovery.Angewandte Chemie (International ed. in English) · 2025Article
- Electronic Structure Tailored Covalent Organic Frameworks for Synergistic Adsorptive-Photocatalytic Gold Recovery from Complex Electronic Waste.Research (Washington, D.C.) · 2025Article
Corrections and comments
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Authors and funding
10 authors.
Funding
Abstract
Gold (Au) concentrations accumulated from electronic waste (e-waste) and industrial leachates far surpass those found in natural ores, a highly valuable resource if efficient recovery methods can be developed. Despite advancements in covalent organic frameworks (COFs), achieving adsorbents with high selectivity, large capacity, and rapid adsorption kinetics remain challenging because of limitations in partial pore wall sites. Here, we present hexaazatriphenylene-based COFs (HATP-COFs) with an electronegative skeleton, specifically designed for selective Au recovery. The hexaazatriphenylene centers, imine linkages, and pyridine linkers within the COFs introduce electron-rich sites that extend across strategic positions-vertex, linkages, and linkers-thereby enhancing the overall structural integrity. These features facilitate efficient Au capture through electrostatic interactions, achieving an exceptional adsorption capacity exceeding 2366 mg g
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Registered trials
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