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“Background Block copolymers
consisting of chemically distinct polymers linked by a covalent bond at one end have the ability to self-assemble into a variety of ordered nanostructures such as lamellae (LAM), hexagonally packed cylinders (HEX), and body-centered cubic (BCC) spheres and more complex structures such as gyroid (G) in melts and Protein Tyrosine Kinase inhibitor solutions [1–7]. This unique characteristic of block copolymers provides possibilities for their potential applications in nanoscience, such as molecular template and nanotubes. Therefore, block copolymers have attracted a great deal of attention both in theory and experiment. Self-assembly and phase separation in diblock copolymers have been well studied both theoretically and experimentally in the last few decades [8–14].