Incorporation of small reactive moieties, the reactivity of which depends on externally imposed load (so-called mechanophores) into polymer chains offers access to a broad range of stress-responsive materials. Here, we report that polymers incorporating spirothiopyran (STP) manifest both green mechanochromism and load-induced addition reactions in solution and solid. Stretching a macromolecule containing colorless STP converts it into green thiomerocyanine (TMC), the mechanically activated thiolate moiety of which undergoes rapid thiol-ene click reactions with certain reactive C=C bonds to form a graft or a cross-link. The unique dual mechanochemical response of STP makes it of potentially great utility both for the design of new stress-responsive materials and for fundamental studies in polymer physics, for example, the dynamics of physical and mechanochemical remodeling of loaded materials.
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http://dx.doi.org/10.1002/anie.201510171 | DOI Listing |
Chem Commun (Camb)
January 2025
State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Fudan University, Shanghai 200438, China.
The synthesis of polymers with well-defined composition, architecture, and functionality has long been a focal area of research in the field of polymer chemistry. The advancement of controlled radical polymerization (CRP) has facilitated the synthesis of precise polymers, which are endowed with new properties and functionalities, thereby exhibiting a wide range of applications. However, radical polymerization faces several challenges, such as oxygen intolerance, and common thermal initiation methods may lead to side reactions and depolymerization.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
School of Materials Science and Engineering, Xiangtan University, Xiangtan, Hunan 411105, P. R. China.
Aerogels are regarded as the next generation of thermal insulators; however, conventional aerogels suffer from issues such as brittleness, low moisture resistance, and a complex production process. Subnanowires (SNWs) are emerging materials known for their exceptional flexibility, toughness, intrinsic hydrophobicity, and gelling capabilities, making them ideal building blocks for flexible, tough, hydrophobic, and thermally insulating aerogels. Herein, we present a simple and scalable strategy to construct SNW aerogels by freeze-drying hydroxyapatite (HAP) SNW dispersions in cyclohexane.
View Article and Find Full Text PDFACS Appl Mater Interfaces
January 2025
Universite de Pau et des Pays de l'Adour, E2S UPPA, CNRS, IPREM, 64053, Pau, France.
The photopolymerization-induced microphase separation (photo-PIMS) process involving a reactive polymer block was implemented to fabricate nanostructured quasi-solid polymer electrolytes (QSPEs) for use in lithium metal batteries (LMBs). This innovative one-pot fabrication enhances interfacial properties in LMBs by enabling nanostructuring of QSPE directly onto the electrodes. This process also allows for customization of QSPE structural dimensions by tweaking the architecture and molar mass of poly[(oligo ethylene glycol) methyl ether methacrylate--styrene] (P(OEGMA--S)) macromolecular chain transfer agent.
View Article and Find Full Text PDFStem Cell Res Ther
January 2025
IRMB, Univ Montpellier, INSERM, CHU St Eloi, 80 AV A Fliche, 34295-Cedex-05, Montpellier, France.
Background: The regenerative potential of mesenchymal stromal/stem cells (MSCs) has been extensively studied in clinical trials in the past decade. However, despite the promising regenerative properties documented in preclinical studies, for instance in osteoarthritis (OA), the therapeutic translation of these results in patients has not been fully conclusive. One factor contributing to this therapeutic barrier could be the presence of senescent cells in OA joints.
View Article and Find Full Text PDFNature
January 2025
Department of Chemistry, University of Manchester, Manchester, UK.
Cells display a range of mechanical activities generated by motor proteins powered through catalysis. This raises the fundamental question of how the acceleration of a chemical reaction can enable the energy released from that reaction to be transduced (and, consequently, work to be done) by a molecular catalyst. Here we demonstrate the molecular-level transduction of chemical energy to mechanical force in the form of the powered contraction and powered re-expansion of a cross-linked polymer gel driven by the directional rotation of artificial catalysis-driven molecular motors.
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