For the electrooxidation of propylene
into 1,2-propylene glycol
(PG), the process involves two key steps of the generation of *OH
and the transfer of *OH to the CC bond in propylene. The strong
*OH binding energy (E
B(*OH)) favors the
dissociation of H2O into *OH, whereas the transfer of *OH
to propylene will be impeded. The scaling relationship of the E
B(*OH) plays a key role in affecting the catalytic
performance toward propylene electrooxidation. Herein, we adopt an
immobilized Ag pyrazole molecular catalyst (denoted as AgPz) as the
electrocatalyst. The pyrrolic N–H in AgPz could undergo deprotonation
to form pyrrolic N (denoted as AgPz-Hvac), which can be
protonated reversibly. During propylene electrooxidation, the strong E
B(*OH) on AgPz favors the dissociation of H2O into *OH. Subsequently, the AgPz transforms into AgPz-Hvac that possesses weak E
B(*OH),
benefiting to the further combination of *OH and propylene. The dynamically
reversible interconversion between AgPz and AgPz-Hvac accompanied
by changeable E
B(*OH) breaks the scaling
relationship, thus greatly lowering the reaction barrier. At 2.0 V
versus Ag/AgCl electrode, AgPz achieves a remarkable yield rate of
288.9 mmolPG gcat
–1 h–1, which is more than one order of magnitude higher
than the highest value ever reported.