“…Sterically hindered amines such as 2,2′‐diethyl‐4,4′‐methylene dianiline,14 4,4′‐methylene‐bis(2,6‐diethyl aniline) (MDEA), and 4,4′‐bis(3‐chloro‐2,6‐diethyl aniline)15 are shown to decrease the basicity of amine. In our previous articles16, 17 the work was carried out on chlorine‐substituted 4,4′‐bis‐(diaminodiphenyl) methane with N , N , N ′, N ′‐tetraglycidyl diaminodiphenyl methane (DDM–TGDDM) systems to study the effect of chlorine substitution and its position on the reactivity of the hardener. We found that chlorine substitution reduces the reactivity of the amine (DDM) and it does so more effectively when substituted at the ortho position.…”