芳基
铱
催化作用
氮化碳
化学
卤化物
光催化
区域选择性
烷基
镍
组合化学
偶联反应
功能群
有机化学
聚合物
作者
Gianvito Vilé,Miguel M. de Vries Ibáñez,Luis A. Cipriano,Giovanni Di Liberto
出处
期刊:Research Square - Research Square
日期:2024-08-11
标识
DOI:10.21203/rs.3.rs-4838220/v1
摘要
Abstract Developing robust and reliable methods for constructing C(sp3)–C(sp3) bonds is critically important for synthesizing a diverse array of functionalized drug molecules. However, this reaction poses significant challenges from a chemical standpoint due to issues with selective activation and regioselectivity, functional group compatibility, complex catalyst design, and slow reaction kinetics. Current metallaphotoredox approaches do not provide a viable solution because they rely on expensive, toxic, and rare iridium photocatalysts, severely limiting their widespread application. In this study, we introduce carbon nitride nanosheets (nC3N4) as an efficient and sustainable alternative to traditional iridium-based catalysts. When combined with nickel catalysis, nC3N4 facilitates the cross-coupling of aryl halides and carboxylic acids. Our results demonstrate a broad substrate scope, including various aryl halides and carboxylic acids, and highlight the recyclability of the photocatalyst. Density functional theory calculations provide molecular insights into the role of nickel single atoms in facilitating photodecarboxylation and subsequent C–C bond formation. This work significantly expands the potential of photoredox chemistry, and offers a novel method for efficient, industrially relevant light-to-chemical conversion processes.
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