Selective chemical recycling of polyhydroxybutyrate into high-value hydroxy acid using the taurine organocatalyst.

Polyhydroxyalkanoates (PHAs) are receiving significant attention due to their biobased origin, biodegradability, and excellent barrier properties. However, their high cost compared to traditional plastics necessitates the development of recycling technologies to retain their value post-use. Despite being thermoplastics, PHAs are difficult to recycle mechanically due to their narrow processing window, particularly for polyhydroxybutyrate (PHB), and conventional chemical recycling routes often lead to non-selective degradation and dehydration to crotonic acid, yielding complex product mixtures with limited valorization potential.

Dual redox-active porous polyimides as high performance and versatile electrode material for next-generation batteries.

Energy storage will be a primordial actor of the ecological transition initiated in the energy and transport sectors. As such, innovative approaches to design high-performance electrode materials are crucial for the development of the next generation of batteries. Herein, a novel dual redox-active and porous polyimide network (MTA-MPT), based on mellitic trianhydride (MTA) and 3,7-diamino--methylphenothiazine (MPT) monomers, is proposed for applications in both high energy density lithium batteries and symmetric all-organic batteries.

Clickable Cisplatin Derivatives as Versatile Tools to Probe the DNA Damage Response to Chemotherapy.

Cisplatin induces DNA crosslinks that are highly cytotoxic. Hence, platinum complexes are frequently used in the treatment of a broad range of cancers. Efficiency of cisplatin treatment is limited by the tumor-specific DNA damage response to the generated lesions.

Hydrothermal polymerization of porous aromatic polyimide networks and machine learning-assisted computational morphology evolution interpretation.

We report on the hydrothermal polymerization (HTP) of polyimide (PI) networks using the medium HO and the comonomers 1,3,5-tris(4-aminophenyl)benzene (TAPB) and pyromellitic acid (PMA). Full condensation is obtained at minimal reaction times of only 2 h at 200 °C. The PI networks are obtained as monoliths and feature thermal stabilities of >500 °C, and in several cases even up to 595 °C.