Precise synthesis and efficient self-assembly of semiconducting polymers are of great interest. Herein, we report the controlled synthesis of π-conjugated poly(phenyl isocyanide)--poly(phenyleneethylene) (PPI--PPE) copolymers via chain extension of ethynyl 4-iodobenzene initiated by Pd(II)-terminated helical poly(phenyl isocyanide) (PPI). The in-situ-generated block copolymers self-assembled into various supramolecular architectures depending on the PPE length. The helical PPI segment induced the block copolymers with an appropriate PPE length self-assemble into helical nanofibers with a controlled size and defined helicity. Interestingly, the chiral assemblies of the block copolymers exhibit intense optical activity and emit clear circularly polarized luminescence.
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http://dx.doi.org/10.1021/acsabm.1c00763 | DOI Listing |
Biomater Sci
January 2025
Zhejiang Key Laboratory of Smart BioMaterials, and College of Chemical and Biological Engineering, Zhejiang University, Hangzhou 310058, China.
Accurate imaging of tumor hypoxia is critical for early cancer diagnosis and clinical outcomes, highlighting the great need for its detection specificity and sensitivity. In this report, we propose a probe (HTRNP) that simultaneously has hypoxia-targeting and hypoxia-responsive capabilities to enhance the tumor hypoxia imaging efficiency. HTRNP was successfully prepared through the encapsulation of Pt(II)-tetrakis(pentafluorophenyl)porphyrin (PtPFPP), which exhibits hypoxia-dependent phosphorescence, within the amphiphilic block copolymer OPDMA-PF, which has hypoxia-targeting tertiary amine -oxide moieties and hydrophobic perfluorobenzene ring structures, which highly improved the loading content and water solubility of PtPFPP.
View Article and Find Full Text PDFMacromol Rapid Commun
January 2025
Chimie ParisTech, CNRS, Institut de Recherche de Chimie Paris, PSL University, Paris, 75005, France.
The development of catalysts that are both robust and highly active at room temperature can often be seen as a major challenge in anionic polymerization. However, these properties are desirable for polymer synthesis because they allow for easy and sustainable production of interesting materials. Here, iron and magnesium complexes are used to form in situ generated metalate complexes that are shown to be highly active in the room temperature copolymerization of methyl methacrylate and lactide.
View Article and Find Full Text PDFChemistry
January 2025
Beijing Institute of Technology, Polymer Materials, 5 Zhongguancun Nandajie, 100081, Beijing, CHINA.
The self-assembly of block copolymers (BCPs) to form nanostructures of various morphologies and controllable dimensions has been a very promising research area in nanotechnology in recent decades. This review mainly summarizes the recent advances in precise and controllable self-assembly of BCPs through a tailored nucleation-growth strategy to modulate the self-assembly behavior of the BCPs. These efforts have led to a better understanding of the self-assembly mechanisms and opened new possibilities for creating novel materials with designable properties.
View Article and Find Full Text PDFJ 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 PDFAngew Chem Int Ed Engl
January 2025
Fudan University, Department of Macromolecular Science, 2205 Songhu Rd, 200438, Shanghai, CHINA.
Nitrogen heterocyclic carbenes (NHCs) are emerging as effective substitutes for conventional thiol ligands in surface functionalization of nanoparticles (NPs), offering exceptional stability to NPs under harsh conditions. However, the highly reactive feature of NHCs limits their use in introducing chemically active groups onto the NP surface. Herein, we develop a general yet robust strategy for the efficient surface functionalization of NPs with copolymer ligands bearing various functional groups.
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