Self-Sorting of Amphiphilic Copolymers for Self-Assembled Materials in Water: Polymers Can Recognize Themselves
Amphiphilic random copolymers bearing hydrophilic poly(ethylene glycol) (PEG) and hydrophobic alkyl pendants showed dynamic self-sorting behavior, that is, self-recognition, under competitive conditions in aqueous media. The self-sorting universally takes place not only in water but also in hydroge...
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Published in | Journal of the American Chemical Society Vol. 141; no. 1; pp. 511 - 519 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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American Chemical Society
09.01.2019
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Abstract | Amphiphilic random copolymers bearing hydrophilic poly(ethylene glycol) (PEG) and hydrophobic alkyl pendants showed dynamic self-sorting behavior, that is, self-recognition, under competitive conditions in aqueous media. The self-sorting universally takes place not only in water but also in hydrogels and on the material surfaces, according to encoded information originating from the primary structure of composition and pendants. Binary blends of the copolymers with different composition or alkyl pendants readily induced composition- or alkyl pendant-dependent self-sorting to simultaneously provide discrete and size-controlled micelles with hydrophobic cores. Surprisingly, the micelles reversibly keep exchanging polymer chains exclusively between identical polymer micelles even in the presence of different counterparts. Owing to the dynamic self-sorting behavior, ABA-triblock copolymers comprising the amphiphilic random copolymer A segments and a hydrophilic PEG chain B segment further provided hydrogels with self-healing yet selectively adhesive properties. |
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AbstractList | Amphiphilic random copolymers bearing hydrophilic poly(ethylene glycol) (PEG) and hydrophobic alkyl pendants showed dynamic self-sorting behavior, that is, self-recognition, under competitive conditions in aqueous media. The self-sorting universally takes place not only in water but also in hydrogels and on the material surfaces, according to encoded information originating from the primary structure of composition and pendants. Binary blends of the copolymers with different composition or alkyl pendants readily induced composition- or alkyl pendant-dependent self-sorting to simultaneously provide discrete and size-controlled micelles with hydrophobic cores. Surprisingly, the micelles reversibly keep exchanging polymer chains exclusively between identical polymer micelles even in the presence of different counterparts. Owing to the dynamic self-sorting behavior, ABA-triblock copolymers comprising the amphiphilic random copolymer A segments and a hydrophilic PEG chain B segment further provided hydrogels with self-healing yet selectively adhesive properties. Amphiphilic random copolymers bearing hydrophilic poly(ethylene glycol) (PEG) and hydrophobic alkyl pendants showed dynamic self-sorting behavior, that is, self-recognition, under competitive conditions in aqueous media. The self-sorting universally takes place not only in water but also in hydrogels and on the material surfaces, according to encoded information originating from the primary structure of composition and pendants. Binary blends of the copolymers with different composition or alkyl pendants readily induced composition- or alkyl pendant-dependent self-sorting to simultaneously provide discrete and size-controlled micelles with hydrophobic cores. Surprisingly, the micelles reversibly keep exchanging polymer chains exclusively between identical polymer micelles even in the presence of different counterparts. Owing to the dynamic self-sorting behavior, ABA-triblock copolymers comprising the amphiphilic random copolymer A segments and a hydrophilic PEG chain B segment further provided hydrogels with self-healing yet selectively adhesive properties. |
Author | Takenaka, Mikihito Imai, Shota Sawamoto, Mitsuo Terashima, Takaya |
AuthorAffiliation | Institute of Science and Technology Research Department of Polymer Chemistry, Graduate School of Engineering RIKEN SPring-8 Center Chubu University Institute for Chemical Research |
AuthorAffiliation_xml | – name: Institute for Chemical Research – name: Department of Polymer Chemistry, Graduate School of Engineering – name: RIKEN SPring-8 Center – name: Institute of Science and Technology Research – name: Chubu University |
Author_xml | – sequence: 1 givenname: Shota surname: Imai fullname: Imai, Shota organization: Department of Polymer Chemistry, Graduate School of Engineering – sequence: 2 givenname: Mikihito surname: Takenaka fullname: Takenaka, Mikihito organization: RIKEN SPring-8 Center – sequence: 3 givenname: Mitsuo orcidid: 0000-0003-0352-9666 surname: Sawamoto fullname: Sawamoto, Mitsuo organization: Chubu University – sequence: 4 givenname: Takaya orcidid: 0000-0002-9917-8049 surname: Terashima fullname: Terashima, Takaya email: terashima@living.polym.kyoto-u.ac.jp organization: Department of Polymer Chemistry, Graduate School of Engineering |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/30507172$$D View this record in MEDLINE/PubMed |
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