“…Due to the easy synthesis, the reported TAMs usually bear electron-donating groups (EDGs) on the para-position of their phenyl arms [4e7]. The losing of the fourth substituent group usually led to the formation of cation, radical or else anion of central carbon, in most cases, if sterically permitted, which would also exist in conjugated tautomeric forms [1,2]. Early researches on the ortho-substituted TAMs are less active because introducing substituents to the ortho position of aryl arms usually needs multi-step reactions [8,9].…”