Nonclassical Block Copolymer Self‐Assembly Resulting from a Constrained Location of Chains and Junctions

Author:

Matsushita Yushu1,Takano Atsushi1,Vayer Marylène2,Sinturel Christophe2ORCID

Affiliation:

1. Department of Molecular and Macromolecular ChemistryGrad. School of EngineeringNagoya University Furo‐cho, Chikusa‐ku Nagoya 464‐8603 Japan

2. InterfacesConfinementMatériaux et Nanostructures (ICMN) UMR 7374CNRS‐Université d'Orléans CS 40059 F‐45071 Orléans France

Publisher

Wiley

Subject

Mechanical Engineering,Mechanics of Materials

Reference70 articles.

1. A more accurate description of the location of the block copolymer junction at the interphase would need to consider interfacial thickness which is given by (χN)−1/2 where χ and N denote the Flory–Huggins interaction parameter and the degree of polymerization of the whole block copolymer respectively.

2. Equilibrium morphology of block copolymer melts

3. Linear and non-linear triblock terpolymers. Synthesis, self-assembly in selective solvents and in bulk

4. Highly Asymmetric Lamellar Nanopatterns via Block Copolymer Blends Capable of Hydrogen Bonding

5. Polydispersity and block copolymer self-assembly

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