The
cleavage of C–O–C linkage is a critical step
in the degradation of diaryl ether contaminants and lignin, which
holds great significance of environmental protection and lignocellulosic
biomass utilization. Traditional chemical cleavage methods require
harsh operation conditions such as using strong acids/bases and/or
at high temperatures. Herein, we report an anodic oxidation process
on the carbon electrode, which displays high efficiency for the selective
electrochemical cleavage of the C–O bond in diaryl ethers under
room conditions. Application of such an electrochemically oxidative
cleavage approach on triclosan, 4-hydroxydiphenyl ether, 4,4′-dihydroxydiphenyl
ether, and rhodamine B demonstrates high reaction selectivity to the
aryl C–O bond. Notably, the production of quinone compounds
as the main products is highlighted to open the opportunity for acquiring
quinone derivatives from diaryl ethers. The anodic oxidation process
is found to apply a direct electrochemical oxidation pattern under
the catalysis of surface oxygenated groups of the carbon electrode.
Enlightened by this finding, a surface modification strategy of the
carbon electrode is proposed to accelerate the oxidative cleavage
of diaryl ethers. The anodic oxidation process not only provides a
novel way to design economic routes for the removal of diaryl ether
contaminants but also has potential application in degrading lignocellulosic
biomass for the production of value-added chemicals.