去甲基化
化学
库仑
联轴节(管道)
催化作用
甲基
偶联反应
分子动力学
催化循环
化学物理
计算化学
群(周期表)
有机化学
材料科学
物理
生物化学
基因表达
量子力学
冶金
DNA甲基化
基因
电子
作者
Xiaoping Zhang,Keke Huang,Yanlin Fu,Ni Zhang,Xianglei Kong,Yuanyuan Cheng,Mingyu Zheng,Yihao Cheng,Tenggao Zhu,Bina Fu,Shouhua Feng,Huanwen Chen
标识
DOI:10.1038/s41467-024-49946-y
摘要
Carbon chain elongation (CCE) is normally carried out using either chemical catalysts or bioenzymes. Herein we demonstrate a catalyst-free approach to promote demethylation C-C coupling reactions for advanced CCE constructed with functional groups under ambient conditions. Accelerated by the electric field, two organic cations containing a methyl group (e.g., ketones, acids, and aldehydes) approach each other with such proximity that the energy of the repulsive Coulomb interaction between these two cations exceeds the bond energy of the methyl group. This results in the elimination of a methyl cation and the coupling of the residual carbonyl carbon groups. As confirmed by high-resolution mass spectrometry and isotope-labeling experiments, the C-C coupling reactions (yields up to 76.5%) were commonly observed in the gas phase or liquid phase, for which the mechanism was further studied using molecular dynamics simulations and stationary-point calculations, revealing deep insights and perspectives of chemistry.
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