Consecutive mechanical-force-induced electron transfer for reduction of aryl halides with high reduction potentials
Abstract Mechanical-force-induced redox catalysis has emerged as a green and expeditous approach in synthetic chemistry, relying on single-electron transfer from polarized piezoelectric materials to substrates initiated by mechanical agitation. However, the piezoelectric potential generated can some...
Saved in:
| Main Authors: | Xiaohong Wang, Xiaochun He, Xuemei Zhang, Qingqing Wang, Qian Huang, Ruiling Qu, Zhong Lian |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
Nature Portfolio
2025-06-01
|
| Series: | Nature Communications |
| Online Access: | https://doi.org/10.1038/s41467-025-60459-0 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Birch reductive arylation by mechanochemical anionic activation of polycyclic aromatic compounds
by: Yoshifumi Toyama, et al.
Published: (2025-05-01) -
On-Surface Ullmann-Type Coupling Reactions of Aryl Halide Precursors with Multiple Substituted Sites
by: Qiwei Liu, et al.
Published: (2025-04-01) -
Unraveling the Electron Transfer in Cupriavidus necator – Insights Into Mediator Reduction Mechanics
by: André Gemünde, et al.
Published: (2024-07-01) -
CuI-Catalyzed: One-Pot Synthesis of Diaryl Disulfides from Aryl Halides and Carbon Disulfide
by: Mohammad Soleiman-Beigi, et al.
Published: (2013-01-01) -
From Harm Reduction to Forced Treatment
by: Aressana Challand
Published: (2025-05-01)