The synthesis of a water soluble azo initiators from 2,2'-azodiisobutyronit
rile (AIBN) was performed in three steps: reaction of dinitrile with aromat
ic alcohols in the presence of HCl to form bisiminoesters hydrochlorides wh
ich are hydrolyzed to the esters and final regioselective sulfonation of th
e aromatic esters. The thermal decomposition of the azo initiators obtained
leads to formation of two surface active radicals which can start the chai
n reaction.