Dimension control on self-assembly of a crystalline core-forming polypeptoid block copolymer: 1D nanofibers versus 2D nanosheets
Author:
Affiliation:
1. Key Laboratory of Biobased Polymer Materials
2. Shandong Provincial Education Department; School of Polymer Science & Engineering
3. Qingdao University of Science and Technology
4. Qingdao
5. China
Abstract
The balance between the crystallization and solubility of the block copolymer dominates the nanostructures.
Funder
National Natural Science Foundation of China
Natural Science Foundation of Shandong Province
Chinese Academy of Sciences
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Polymers and Plastics,Biochemistry,Bioengineering
Link
http://pubs.rsc.org/en/content/articlepdf/2021/PY/D0PY01673J
Reference38 articles.
1. Crystallization-Driven Self-Assembly of Block Copolymers with a Short Crystallizable Core-Forming Segment: Controlling Micelle Morphology through the Influence of Molar Mass and Solvent Selectivity
2. Supramolecular Assemblies of Amphiphilic Homopolymers
3. A Convenient Method of Tuning Amphiphilic Block Copolymer Micellar Morphology
4. Tailoring the amphiphilicity and self-assembly of thermosensitive polymers: end-capped PEG–PNIPAAM block copolymers
5. Self-Assembly of Organometallic Block Copolymers: The Role of Crystallinity of the Core-Forming Polyferrocene Block in the Micellar Morphologies Formed by Poly(ferrocenylsilane-b-dimethylsiloxane) in n-Alkane Solvents
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