This manuscript is dedicated to Professor Mitsuo Sawamoto's outstanding achievements in polymer chemistry and recognizes his recent retirement from 40 years of exceptional service to Kyoto University. ABSTRACT: In this work, we examined the synthesis of novel block (co)polymers by mechanistic transformation through anionic, cationic, and radical living polymerizations using terminal carbonhalogen bond as the dormant species. First, the direct halogenation of growing species in the living anionic polymerization of styrene was examined with CCl 4 to form a carbon-halogen terminal, which can be employed as the dormant species for either living cationic or radical polymerization. The mechanistic transformation was then performed from living anionic polymerization into living cationic or radical polymerization using the obtained polymers as the macroinitiator with the SnCl 4 /n-Bu 4 NCl or RuCp * Cl(PPh 3 )/Et 3 N initiating system, respectively. Finally, the combination of all the polymerizations allowed the synthesis block copolymers including unprecedented gradient block copolymers composed of styrene and p-methylstyrene.Meanwhile, the mechanistic transformation among the various growing active species during living polymerizations can overcome the limitation of polymerizable monomers to form block copolymers composed of different type of monomers. [22][23][24][25][26] As Additional supporting information may be found in the online version of this article.