Nucleophilic Construction of Sulfate Bond: A Simplified Access to Polysulfates and Polysulfonates
We herein report a concise process to quantitative synthesis of polysulfates and pollysulfonates through the nucleophilic substitution between aryl phenols and aryl fluorosulfates in the presence of inorganic bases such as K2CO3, Na2CO3, K3PO4, Cs2CO3 etc. The reaction we developed was carried out without pre-preparation of phenolates or further modification of aryl phenols with “Si” groups (for example, TMS and TBS groups) which made a sharply reduction of the production costs both in lab research and industrial manufacture. The aryl phenolates were formed in-situ and the process was moisture and air stable. Applying this process, polysulfates and polysulfonates with the properties of high molecular weight, narrow polydispersity, kg-scale and functional group tolerance were prepared. The byproducts of our process were water and fluorides. Several physical and chemical properties of the polymer were evaluated. Also, P-1 could be synthesized through a one-pot process in the presence of BPA, base and SO2F2. The distinct advantages of our protocol made it a more valuable mode in future industrial applications of synthesis of polysulfates and polysulfonates, as well as the formation of sulfate bond.