Based on the highly disparate reactivities of isoprene (I, = 25.4) and 4-methylstyrene (4MS, = 0.007) in the anionic copolymerization in nonpolar media, a general strategy for the rapid and scalable synthesis of tapered multiblock copolymers with an extremely steep gradient has been developed. A repetitive addition strategy of a mixture of isoprene and 4MS leads to a tapered diblock in each case, giving access to linear alternating multiblock copolymers of the (AB) type with up to 10 blocks. All multiblock copolymers showed narrow molecular weight distributions (dispersity = 1.04-1.12). High molecular weights in the range of 80 to 400 kg mol were achieved. Due to the incompatibility of PI and P4MS segments, the multiblock copolymers exhibit nanophase separation, manifested by separate glass transitions for both constituents. Stress-strain measurements revealed extraordinary toughness and elongations up to 1150% strain at break, even at a 50/50 molar ratio I/4MS (i.e., 37 wt% isoprene). Our synthesis permits access to a wide range of tapered multiblock copolymer architectures with rigid (P4MS, high glass transition, ) and flexible (low ) chains, in /2 steps, while keeping overall dispersity low.
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http://dx.doi.org/10.1021/acsmacrolett.8b00390 | DOI Listing |
J Am Chem Soc
January 2025
State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.
While synthesizing circular polymers with telechelic polyolefin building blocks recently emerged as a promising strategy for addressing conventional polyethylenes' sustainability challenges, the lack of telechelic PP (PP) with sufficient difunctional purity for polycondensation has been limiting the development of circular polypropylenes with PP-like structures and properties. Here we described a combined approach of coordinative chain transfer polymerization and transition-metal-catalyzed quenching reaction with various acyl chlorides, affording PPs with a high difunctional ratio (up to ∼99%) and broad end functional group scope. The steric effect of polymeryl-Zn species and the role of Pd catalyst were revealed by DFT.
View Article and Find Full Text PDFBiomater Adv
January 2025
Maastricht University, MERLN Institute for Technology-Inspired Regenerative Medicine, Complex Tissue Regeneration Department, 6229 ER Maastricht, the Netherlands. Electronic address:
Bone-healing complications can occur due to large bone defects or an insufficient bone regeneration capacity. Melt electrowriting (MEW) is a potential candidate for manufacturing synthetic scaffolds that may resolve bone-healing complications. MEW can exploit various biocompatible polymers with a wide range of tissue engineering applications.
View Article and Find Full Text PDFMolecules
December 2024
Laboratory of Chemistry and Technology of Polymers and Colors, Department of Chemistry, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece.
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers was achieved through Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR), ensuring the successful integration of PEF and PCL segments. X-ray Photoelectron Spectroscopy (XPS) was employed for chemical bonding and quantitative analysis, providing insights into the distribution and compatibility of the copolymer components.
View Article and Find Full Text PDFMacromol Biosci
January 2025
Cluster for Advanced Macromolecular Design (CAMD) and Australian Centre for NanoMedicine (ACN), School of Chemical Engineering, UNSW, Sydney, NSW, 2052, Australia.
Invasive fungal infections cause over 3.7 million deaths worldwide annually, underscoring the critical need for new antifungal agents. Developing selective antifungal agents is challenging due to the shared eukaryotic nature of both fungal and mammalian cells.
View Article and Find Full Text PDFACS Nano
January 2025
Department of Chemistry, University of Minnesota, Minneapolis, Minnesota 55455, United States.
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