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In this work, we studied the equilibrium structures formed by a single (AB) multiblock copolymer chain. Within our model, the interactions between the A-type beads were repulsive and the B-type beads could form pairwise reversible bonds with each other (BB-bonds). Our goal was to investigate how the formation of pairwise reversible bonds between the A-type beads and the B-type beads (AB-bonds) affected the structure of the chain. We observed the formation of well-studied intramolecular micelles when the AB-bonds were absent; however, the chain folding changed dramatically when the formation of the AB-bonds was introduced. In this case, the multiblock copolymer formed a globule, which had a unique heterogeneous checkerboard-like distribution of the contact density. We discovered that contacts of beads of different types (i.e., AB-contacts) occurred much more frequently than contacts of beads of the same type (i.e., AA- and BB-contacts) in these structures. This effect can be explained by a simple model of chemical equilibrium in a two-component fluid of reversibly interacting particles, which can be solved exactly. This novel type of folding can serve as a basic model for any (AB) multiblock copolymer chain with a non-vanishing attraction between A and B blocks.
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http://dx.doi.org/10.1063/5.0072568 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA.
Adhesives are important in creating multilayer products, such as in packaging and construction. Most current hot-melt adhesives such as poly(ethylene-co-vinyl acetate) (EVA) and polyurethanes lack chemical recyclability and do not easily de-bond, complicating recycling. Here, we achieved tunable adhesive properties of chemically recyclable polyolefin-like multiblock copolymers through regulating the incorporation of crystalline hard blocks, amorphous soft blocks, and ester content highlighted by adhesive strengths up to 6.
View Article and Find Full Text PDFSci Rep
September 2025
Eldivan Vocational School of Health Services, Department of Medical Services and Techniques, Cankiri Karatekin University, Çankırı, Turkey.
The branched multiblock copolymer based on fatty acid, methyl methacrylate and PHB was first time synthesized. Autoxidation is the reaction of unsaturated fatty acids with air oxygen leading to macroperoxide initiators. Poly (3-hydroxy butyrate), PHB, is a natural bio polyester accumulated in the bacterium cell of some bacteria.
View Article and Find Full Text PDFACS Macro Lett
August 2025
Laboratory of Self-Organizing Soft Matter, Department of Chemical Engineering and Chemistry and Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, 5600 MB, Eindhoven, The Netherlands.
Control over the composition and sequence of synthetic copolymers represents one of the most challenging targets in modern polymer science, in particular, for the labor- and time-consuming preparation of copolymers bearing ionic moieties. Though so far primarily focused on the assembly of coacervate nanostructures, we leverage polymerization-induced electrostatic self-assembly (PIESA) to achieve control over the composition and sequence of neutral-ionic copolymers and create complex chain topologies from equimolar mixtures of neutral and ionic monomers in a direct, one-pot process in aqueous solution. We are making use of the selective recruitment of charged over neutral monomers on an oppositely charged template to modulate monomer reactivities during a controlled radical polymerization by creating segregated reaction environments.
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials Oriented Chemical Engineering, Dalian University of Technology, Dalian 116024, China.
The increasing accumulation of plastic waste in the environment brings about a potential danger for ecosystems and human society; mechanical recycling remains one of the most economical strategies to deal with the growing crisis of plastic pollution; however, it suffers from substantial performance deterioration when processing immiscible blends of polyethylene and nylon plastics. Here, we report on-demand nonalternating copolymerization of ethylene with carbon monoxide (CO) via a facile tandem gas compensation strategy, which achieves a precision control over carbonyl incorporation with uniform distribution across a broad range (0-50%). Such a synthetic advance offers a unique multiblock structure having short polar segments ((CH-CH)-CO-) ( < 4) and extended nonpolar methylene sequences ( > 4).
View Article and Find Full Text PDFJ Am Chem Soc
July 2025
Department of Chemistry, University of Southern California, Los Angeles, California 90007, United States.
Block copolymers of polyethylene (PE) and polyvinyl chloride (PVC) have remained elusive materials despite PE and PVC being the first and third most produced polymers globally, respectfully. The closest material is chlorinated polyethylene (CPE), which is commonly used as a compatibilizer and is synthesized by functionalizing PE. However, there does not exist a synthetic pathway either from monomers or via the functionalization of PE to yield a polymer that has a controlled chlorine amount and primary structure along the polymer chain.
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