“…[1,2] Amphiphilic block copolymers, on one hand which generally built with hydrophilic blocks and hydrophobic moieties in covalent linkage, would assemble into micelles, vesicles, or lamellar ordered structures in aqueous solution, [3] has been widely investigated both from theoretical design to practical applications such as molecular delivery vehicles, [2][3][4] single-chain folding behavior, [5] single chain nanoparticles [1] and the like. [6] On the other hand, block copolymer assemblies constructed from noncovalent associative polymer, [7] especially host-guest driven self-assembly, which avoids complicated synthesis and cumbersome purification procedures, is chosen to form micelles, [8,9] vesicles, [10] hydrogels, [11] or nanofibers [12] . Furthermore, significant efforts have been made to explore conformational evolution of self-assembly via supramolecular polymers derived from linear, [13] hyperbranched, [14] star [15,16] or comb shape [17] polymers through the interaction of hostguest polymer or oligomers.…”