Outside Back Cover: Sulfur Conversion to Donor‐Acceptor Ladder Polymer Networks Through Mechanochemical Nucleophilic Aromatic Substitution for Efficient CO <sub>2</sub> Photoreduction (Angew. Chem. Int. Ed. 20/2025)

A novel mechanochemical-assisted approach converts elemental sulfur into thianthrene-bridged porous ladder polymers with dense donor-acceptor (D-A) junctions, mimicking natural leaves for efficient CO2 photoreduction with H2O, without additional photosensitizers, sacrificial agents, or cocatalysts. The key innovation is a mechanochemical nucleophilic aromatic substitution (SNAr) reaction, enabling sustainable solid-state condensation of sulfur with 1,2-dihaloarenes to form bent thianthrene units. For details read the Research Article by Xiang Zhu, Xin-Ping Wu, Chengcheng Tian, Sheng Dai et al. (e202419108).

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-04-17
DOI
https://doi.org/10.1002/anie.202507727
Citations
1
Primary Topic
Carbon dioxide utilization in catalysis
Type
article
Field-Weighted Citation Impact
0.70
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article

Outside Back Cover: Sulfur Conversion to Donor‐Acceptor Ladder Polymer Networks Through Mechanochemical Nucleophilic Aromatic Substitution for Efficient CO 2 Photoreduction (Angew. Chem. Int. Ed. 20/2025)

Chengcheng Tian, Xiang Zhu, Sheng Dai, Na Yang et al.
1 citations
Angewandte Chemie International Edition
Carbon dioxide utilization in catalysis
0.70
article

Outside Back Cover: Sulfur Conversion to Donor‐Acceptor Ladder Polymer Networks Through Mechanochemical Nucleophilic Aromatic Substitution for Efficient CO 2 Photoreduction (Angew. Chem. Int. Ed. 20/2025)

Chengcheng Tian, Xiang Zhu, Sheng Dai, Na Yang, Xin‐Ping Wu, Jiwei Wu, Yifan Zhang, Tao Wang, Xia Jiang, Zijian Zhou
article en
1 citations

Abstract

A novel mechanochemical-assisted approach converts elemental sulfur into thianthrene-bridged porous ladder polymers with dense donor-acceptor (D-A) junctions, mimicking natural leaves for efficient CO2 photoreduction with H2O, without additional photosensitizers, sacrificial agents, or cocatalysts. The key innovation is a mechanochemical nucleophilic aromatic substitution (SNAr) reaction, enabling sustainable solid-state condensation of sulfur with 1,2-dihaloarenes to form bent thianthrene units. For details read the Research Article by Xiang Zhu, Xin-Ping Wu, Chengcheng Tian, Sheng Dai et al. (e202419108).

Angewandte Chemie International EditionVol. 64(20)
Shanghai University (CN), Oak Ridge National Laboratory (US), East China University of Science and Technology (CN), Sichuan University (CN)
Openalex Percentile: Top 37%
Carbon dioxide utilization in catalysis
0.70
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Outside Back Cover: Sulfur Conversion to Donor‐Acceptor Ladder Polymer Networks Through Mechanochemical Nucleophilic Aromatic Substitution for Efficient CO <sub>2</sub> Photoreduction (Angew. Chem. Int. Ed. 20/2025) — Chengcheng Tian, Xiang Zhu, et al. · Angewandte Chemie International Edition (2025) | TGRS Research Map | TGRS