| Autor: |
Patra, Tuhin, Arepally, Sagar, Seitz, Jakob, Wirth, Thomas |
| Předmět: |
|
| Zdroj: |
Nature Communications; 7/27/2024, Vol. 15 Issue 1, p1-8, 8p |
| Abstrakt: |
Electrochemistry offers tunable, cost effective and environmentally friendly alternatives to carry out redox reactions with electrons as traceless reagents. The use of organoiodine compounds as electrocatalysts is largely underdeveloped, despite their widespread application as powerful and versatile reagents. Mechanistic data reveal that the hexafluoroisopropanol assisted iodoarene oxidation is followed by a stepwise chloride ligand exchange for the catalytic generation of the dichloroiodoarene mediator. Here, we report an environmentally benign iodine(I/III) electrocatalytic platform for the in situ generation of dichloroiodoarenes for different reactions such as mono- and dichlorinations as well as chlorocyclisations within a continuous flow setup. Electrochemistry offers tunable, cost effective and environmentally friendly alternatives to carry out redox reactions but the use of organoiodine compounds as electrocatalysts is largely underdeveloped. Here, the authors report an environmentally benign iodine(I/III) electrocatalytic platform for the in situ generation of dichloroiodoarenes for different reactions within a continuous flow setup. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
|
Full text from SpringerLink