Carbon dot-based type I photosensitizers for photocatalytic oxidation reaction of arylboric acid and N-phenyl tetrahydroisoquinoline

IF 4.9 2区 化学 Q2 CHEMISTRY, PHYSICAL Molecular Catalysis Pub Date : 2024-10-21 DOI:10.1016/j.mcat.2024.114625
Zhong-Lin Guo , Kai-kai Niu , Yu-Guang Lv , Ling-Bao Xing
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Abstract

Carbon dots (CDs) have emerged as promising materials for photocatalytic organic transformations due to their excellent photostability, tunable electronic properties, and environmental friendliness; However, the ability of CDs to selectively generate reactive oxygen species (ROS) and its integration with organic photocatalytic synthesis applications has always been a long-term challenge. In this work, we synthesized a new nitrogen and phosphorus co-doped carbon dots (N,P-CDs) with enhanced light absorption and notable efficiency in generating superoxide anion (O2•−) selectively. Leveraging the selective generation of superoxide anions, we achieved highly efficient photooxidation of boronic acids and N-phenyl tetrahydroisoquinolines, demonstrating the practical applicability of N,P-CDs as photocatalysts and represents good functional-group tolerance as well as a broad substrate scope. This study provides valuable insights into the design of carbon-based photocatalysts with controlled ROS generation, opening new avenues for environmentally benign organic transformations.

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用于芳基硼酸和 N-苯基四氢异喹啉光催化氧化反应的 I 型碳点光敏剂
碳点(CD)因其优异的光稳定性、可调的电子特性和环境友好性,已成为光催化有机转化的理想材料;然而,碳点选择性生成活性氧(ROS)的能力及其与有机光催化合成应用的结合一直是一个长期的挑战。在这项工作中,我们合成了一种新的氮磷共掺杂碳点(N,P-CDs),它具有更强的光吸收能力和选择性生成超氧阴离子(O2--)的显著效率。利用超氧阴离子的选择性生成,我们实现了硼酸和 N-苯基四氢异喹啉的高效光氧化,证明了 N,P-CDs 作为光催化剂的实用性,并代表了良好的官能团耐受性和广泛的底物范围。这项研究为设计可控 ROS 生成的碳基光催化剂提供了宝贵的见解,为环境无害的有机转化开辟了新途径。
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来源期刊
Molecular Catalysis
Molecular Catalysis Chemical Engineering-Process Chemistry and Technology
CiteScore
6.90
自引率
10.90%
发文量
700
审稿时长
40 days
期刊介绍: Molecular Catalysis publishes full papers that are original, rigorous, and scholarly contributions examining the molecular and atomic aspects of catalytic activation and reaction mechanisms. The fields covered are: Heterogeneous catalysis including immobilized molecular catalysts Homogeneous catalysis including organocatalysis, organometallic catalysis and biocatalysis Photo- and electrochemistry Theoretical aspects of catalysis analyzed by computational methods
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