Quantum Dot Interface-Enabled Cross-Coupling Acylation by Direct Aldehyde Activation under Visible Light
Source abstract
Abstract
Cross-coupling acylation by direct aldehyde activation is ideal to construct a useful carbonyl motif. However, the strong C-H bond energy, short radical lifetime, and mismatched radical polarity render this reaction a huge challenge. Herein, the semiconductor quantum dots (QDs) interface is demonstrated to overcome the obstacles lying on the way to acylating alkene or alkylarene, directly activating the formyl C-H bond into an acyl radical. Further stabilization of the obtained radical species by the QD interface ensured their effective cross-coupling with the generated intermediate from the coupling partner. The interface of QDs was exemplified to execute photochemical transformation, showcasing a highly efficient and selective cross-coupling acylation reaction under extremely mild conditions.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Radical Photochemical Reactions · Perovskite Materials and Applications · Sulfur-Based Synthesis Techniques
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Key Laboratory of Photochemical Conversion and Optoelectronic Materials, New Cornerstone Science Laboratory, Technical Institute of Physics and Chemistry
Chinese Academy of Sciences
School of Future Technology
University of Chinese Academy of Sciences
Funding
National Key Research and Development Program of China · Natural Science Foundation of Beijing Municipality · National Natural Science Foundation of China · Natural Science Foundation of Shandong Province · Chinese Academy of Sciences · New Cornerstone Science Foundation
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