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Membrane-Free Electrosynthesis of Epichlorohydrins Mediated by Bromine Radicals over Nanotips.
Gao, Ying; Yan, Mingming; Cheng, Chuanqi; Zhong, Hao; Zhao, Bo-Hang; Liu, Cuibo; Wu, Yongmeng; Zhang, Bin.
Affiliation
  • Gao Y; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Yan M; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Cheng C; Institute of New Energy Materials, School of Materials Science and Engineering, Tianjin University, Tianjin 300072, China.
  • Zhong H; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Zhao BH; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Liu C; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Wu Y; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
  • Zhang B; Department of Chemistry, School of Science, Institute of Molecular Plus, Tianjin University, Tianjin 300072, China.
J Am Chem Soc ; 146(1): 714-722, 2024 Jan 10.
Article in En | MEDLINE | ID: mdl-38157544
ABSTRACT
The industrial manufacture of epichlorohydrin (ECH) often suffers from excessive corrosive chlorine and multistep processes. Here, we report a one-pot membrane-free Br radical-mediated ECH electrosynthesis. Bromine radicals electro-oxidized from Br- ions initiate the reaction and then eliminate HBr from bromohydrin to give ECH and release Br- ions for reuse. A high energy barrier for *OH oxidation and isolated Br adsorption sites enables NiCo2O4 to suppress the competitive oxygen and bromine evolution reactions. The high-curvature nanotips with an increased electric field concentrate Br- and OH- ions to accelerate ECH electrosynthesis. This strategy delivers ECH with a Faradaic efficiency of 47% and a reaction rate of 1.4 mol h-1 gcat-1 at a high current density of 100 mA cm-2, exceeding the profitable target from the techno-economic analysis. Economically profitable electrosynthesis, methodological universality, and the extended synthesis of epoxide-drug blocks highlight their promising potential.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: China

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Am Chem Soc Year: 2024 Document type: Article Affiliation country: China