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通过供体结构设计调控咔唑共轭微孔聚合物上的载流子转移以实现硫酚的功能化

Modulating Carrier Transfer over Carbazolic Conjugated Microporous Polymers via Donor Structural Design for Functionalization of Thiophenols.

作者信息

Zhang Weijie, Peng Qi, Yang Hai, Fang Zhengjun, Deng Jiyong, Yu Guipeng, Liao Yunfeng, Liao Shuzhen, Liu Qingquan

机构信息

Hunan Provincial Key Laboratory of Environmental Catalysis and Waste Recycling, School of Chemistry and Chemical Engineering, Hunan Institute of Engineering, Xiangtan 411104, People's Republic of China.

Hunan Provincial Key Lab of Advanced Materials for New Energy Storage and Conversion, Hunan University of Science and Technology, Xiangtan 411201, People's Republic of China.

出版信息

ACS Appl Mater Interfaces. 2021 Dec 22;13(50):60072-60083. doi: 10.1021/acsami.1c20579. Epub 2021 Dec 9.

Abstract

Developing photocatalysts to steer conversion of solar energy toward high-value-added fine chemicals represents a potentially viable approach to address the energy crisis and environmental issues. However, enablement of this conversion is usually impeded by the sluggish kinetic process for proton-coupled electron transfer and rapid recombination of photogenerated excitons. Herein, we report a simple and general structural expansion strategy to facilitate charge transfer in conjugated microporous polymers (CMPs) via engineering the donor surrounding the trifluoromethylphenyl core. The resulting CMPs combine high surface area, strong light-harvesting capabilities, and tunable optical properties endowed by extended π-conjugation; the optimized compound CbzCMP-5 generated from 9,9',9″-(2-(trifluoromethyl)benzene-1,3,5-triyl)tris(9-carbazole) remarkably enhanced the photogenerated carrier transfer efficiency, enabling the functionalization of thiophenols toward thiocarbamates and 3-sulfenylindoles with high photocatalytic efficiency. Most importantly, the in-depth insights into the carrier-transfer processes open up new prospects on further optimization and rational design of photoactive polymers for efficient charge-transfer-mediated reactions.

摘要

开发光催化剂以引导太阳能转化为高附加值精细化学品是解决能源危机和环境问题的一种潜在可行方法。然而,这种转化通常受到质子耦合电子转移的缓慢动力学过程和光生激子的快速复合的阻碍。在此,我们报告了一种简单且通用的结构扩展策略,通过设计围绕三氟甲基苯基核心的供体来促进共轭微孔聚合物(CMPs)中的电荷转移。所得的CMPs具有高表面积、强吸光能力以及由扩展π共轭赋予的可调光学性质;由9,9',9″-(2-(三氟甲基)苯-1,3,5-三基)三(9-咔唑)生成的优化化合物CbzCMP-5显著提高了光生载流子转移效率,能够以高光催化效率将苯硫酚官能化为硫代氨基甲酸盐和3-亚磺酰基吲哚。最重要的是,对载流子转移过程的深入洞察为进一步优化和合理设计用于高效电荷转移介导反应的光活性聚合物开辟了新前景。

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