Expeditious base-free solid-state reaction between phenyl boronates and hydrogen peroxide on silica gel

The conversion of phenyl boronates to phenol with hydrogen peroxide (H2O2) usually requires a base as a chemical assistant. In this work, we reported a base-free reaction between a phenyl boronate thin film and H2O2 vapor on a nanostructured silica gel surface and the yield is determined as 80% in 25 s. A fluorescent compound C6NIB was used to monitor the reaction process in both solution and the solid state. The fluorescent tests suggested that the silica gel surface can effectively promote the phenyl boronate compound reacting with H2O2 immediately on the solid state. Through control experiments, we determined the optimal reaction conditions. SEM, BET and water vapor adsorption characterization illustrated that the evenly distributed nanoscale pores and large surface areas of the silica gel interface may be critical for catalysis. Moreover, UV-vis absorption and reflection spectroscopy revealed that the final product of the base-free reaction was neutral phenol, instead of phenolate under basic conditions. Compared with traditional base-in reactions, the newly reported silica gel involved surface reaction could significantly extend the lifetime of the indicator molecules, resulting in excellent storage performance for practical sensing application. Finally, the simulation experiments identified the HO2-/H3O+ ionic pair on the interacting Si-OH surface group pairs on the silica surface as the key for catalysis. Thus, the generated HO2- then in turn reacted with phenyl boronate to form a phenol structure. The nanosized pores, arranged hydrogen bonding, and organized surface interface together led to this expeditious and effective base-free reaction between boronates and H2O2.

Automated summary

The study reported a base-free conversion of phenyl boronates to phenol with H2O2 on a nanostructured silica gel surface, achieving a high yield of 80% within 25 seconds. The silica gel surface was found to effectively promote the reaction and extend the lifetime of indicator molecules, leading to excellent storage performance. The key for catalysis was identified as the HO2-/H3O+ ionic pair on the Si-OH surface groups, facilitating the rapid and efficient base-free reaction.