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In the last decade, the application of dynamic covalent chemistry in the field of polymeric materials has become the subject of an increasing number of studies, gaining applicative relevance. This is due to the fact that polymers containing dynamic functions possess a structure that affords reprocessability, recyclability and peculiar self-healing properties inconceivable for "classic" polymer networks. Consequently, the synthesis of a dynamic covalent chemistry-based polymer and its chemical, thermal, and mechanical characterizations are reported in the present research. In particular, oleic acid has been used as starting material to follow the founding principles of the circular economy system and, thanks to the aromatic disulfide component, which is the foundation of the material dynamic characteristics, the obtained polymer resulted as being reprocessable and self-healable. Moreover, the polymer can strongly interact with copper surfaces through the formation of stable Cu-S bonds. Then, the application of the polymer as a solvent-free reusable adhesive for copper was investigated by lap joint shear tests and comparisons with the properties of an analogous material, devoid of the disulfide bonds, were conducted.
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http://dx.doi.org/10.3390/polym14224919 | DOI Listing |
Chem Commun (Camb)
September 2025
Department of Chemistry Indian Institute of Technology, Kharagpur 721302, India.
A copper(II) metalorganic hydrogel has been synthesised using the ligand ((2-hydroxynaphthalen-1-yl)methyl)-L-threonine and characterised. The hydrogel is an efficient, reusable catalyst for the selective synthesis of 1,3-oxathiolane-2-thiones from the reaction of CS and epoxides under solvent-free conditions.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Department of Industrial and Engineering Chemistry, Institute of Chemical Technology, Mumbai- Marathwada Campus, Jalna, Maharashtra, 431213, India.
Industrial hydrogenation is a pivotal process in chemical synthesis. However, it has significant drawbacks, including high cost, safety risks associated with the use of molecular hydrogen gas, and substantial energy demands due to the need for elevated temperatures and pressures to achieve satisfactory yields. The borrowing hydrogen synthesis, which enables the transfer of hydrogen between molecules, offers a promising approach for green, one-pot synthesis of industrially important chemicals and intermediates.
View Article and Find Full Text PDFMater Horiz
July 2025
State Key Laboratory of Advanced Marine Materials, Zhejiang Key Laboratory of Marine Materials and Protective Technologies, Ningbo Institute of Materials Technology and Engineering, Chinese Academy of Sciences, Ningbo 315201, P. R. China.
Supramolecular polymer adhesives (SPA) based on dynamic non-covalent interactions exhibit a wide range of potential applications. However, achieving on-demand adhesion by precisely adjusting non-covalent interactions to achieve successful adhesion in a variety of situations has long been a challenge. Here we report a facile method to develop SPA based on natural molecules of lipoic acid (LA) and hydroxypropyl β-cyclodextrin (hCD) with tailored adhesion behavior and unique time-temperature dependent characteristics for on-demand adhesion in multiple scenarios.
View Article and Find Full Text PDFRSC Adv
July 2025
Department of Chemistry, Kr.V.N. Naik Shikshan Prasarak Sanstha's Arts, Commerce and Science College, Savitribai Phule Pune University Canada Corner Nashik - 422 002 Maharashtra India.
The advancement of green and efficient synthetic strategies is essential for the pursuit of environmentally sustainable organic transformations. Pyrazole derivatives, recognized for their broad pharmacological and synthetic utility, are key structural motifs in various bioactive molecules. This study reports a one-pot, four-component (aryl aldehyde, malononitrile, ethyl acetoacetate, and hydrazine hydrate) synthesis of pyrazole derivatives catalyzed by lanthanum-doped and silver-coated ZnO (Ag/La-ZnO) core-shell nanoparticles under solvent-free grinding conditions at ambient room temperature.
View Article and Find Full Text PDFJ Org Chem
August 2025
School of Chemistry, South China Normal University, Guangzhou 510006, China.
We present a sustainable and safe method for synthesizing aromatic ketones and biphenyls using quartz sand as a green medium. Quartz sand replaces traditional solvents, providing a safer, eco-friendly alternative in Suzuki-Miyaura coupling and decarbonylative coupling reactions. The Suzuki-Miyaura coupling reactions occur under mild, solvent-free conditions with efficient synthesis and easy purification.
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