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Hybrid materials (HMs) combine the high diversity of functionalities of organic compounds with properties typical for inorganic materials, such as high mechanical strength or high thermal stability. Herein, HMs combining organic pigment molecules and TiO2 as inorganic component, with covalently linked components, i.e., so‐called class II HMs, are reported. The synthesis of such HMs is intrinsically challenging, as the apolar organic pigment component and the inorganic polar TiO2 component require different conditions for their respective formation. Herein, we circumvent this issue by employing solvothermal synthesis in superheated isopropanol, which through temperature tunability of the solvent properties allows for both generating and linking both components in one‐pot. First, it is shown that an organic benzimidazole‐based pigment molecule designed for readily binding to Ti can be synthesized solvothermally. Second, new class II titanium‐based HMs are generated from Ti(OiPr)4 and pigment precursors in a solvothermal reaction. The pigment@TiO2 HMs feature significant porosity and are structurally identified as layered structures of lepidocrocite‐like TiO2 linked via pigment molecules. These layered HMs assemble into hierarchical nanoflowers, and depending on the pigment segments, different interlayer spacings in between inorganic layers are observed. Third, the pigment@TiO2 materials are shown to be usable as electrode materials in lithium‐ion batteries.

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. We reasoned that better tools to investigate the repair of DNA crosslinks induced by cisplatin would therefore be highly useful in addressing drug limitations. Here, we synthesized a series of cisplatin derivatives that are compatible with click chemistry, thus allowing visualization and isolation of DNA-platinum crosslinks from cells to study cellular responses. We prioritized one alkyne and one azide Pt(II) derivative, Pt-alkyne-53 and Pt-azide-64, for further biological characterization. We demonstrate that both compounds bind DNA and generate DNA lesions and that the viability of treated cells depends on the active DNA repair machinery. We also show that the compounds are clickable with both a fluorescent probe as well as biotin, thus they can be visualized in cells, and their ability to induce crosslinks in genomic DNA can be quantified. Finally, we show that Pt-alkyne-53 can be used to identify DNA repair proteins that bind within its proximity to facilitate its removal from DNA. The compounds we report here can be used as valuable experimental tools to investigate the DNA damage response to platinum complexes and hence might shed light on mechanisms of chemoresistance.

Biogenic metal oxides (MxOy) feature structures as highly functional and unique as the organisms generating them. They have caught the attention of scientists for the development of novel materials by biomimicry. In order to understand how biogenic MxOy could inspire novel technologies, we have reviewed examples of all biogenic MxOy, as well as the current state of understanding of the interactions between the inorganic MxOy and the biological matter they originate from and are connected to. In this review, we first summarize the origins of the precursors that living nature converts into MxOy. From the point-of-view of our materials chemists, we present an overview of the biogenesis of silica, iron and manganese oxides, as the only reported biogenic MxOy to date. These MxOy are found across all five kingdoms (bacteria, protoctista, fungi, plants and animals). We discuss the key molecules involved in the biosynthesis of MxOy, the functionality of the MxOy structures, and the techniques by which the biogenic MxOy can be studied. We close by outlining the biomimetic approaches inspired by biogenic MxOy materials and their challenges, and we point at promising directions for future organic-inorganic materials and their synthesis.

Los colorantes orgánicos son una clase de compuestos comerciales muy importantes que se caracterizan, principalmente, por la presencia de grupos conjugados y funciones que generan color (cromóforos) como los grupos carbonilo, azo o nitroso. Estos compuestos encuentran diversas aplicaciones en la coloración de todo tipo de sustancias, desde plásticos hasta textiles; sin embargo, las rutas sintéticas de dichos compuestos son a menudo muy tóxicas y nocivas para el medio ambiente. Esta revisión explica, en primer lugar, las bases fisicoquímicas de los colorantes y sigue con una introducción a las clasificaciones y síntesis generales. Finalmente, se destacan los nuevos avances en la síntesis hidrotermal de colorantes de alto rendimiento.

Los polímeros de alto rendimiento (HPP) desempeñan un rol importante en la actualidad. El desarrollo de métodos más eco­nómicos para sintetizar estos polímeros minimizando el impacto tanto en la salud como en el medio ambiente es una prioridad. Las poliimidas (PI) pertenecen al grupo de los HPP y presentan características excepcionales como una gran estabilidad ante elevadas temperaturas, alta resistencia a los productos químicos agresivos y a la radiación, así como propiedades de aislamiento. Sin embargo, la síntesis de las PI presenta aún retos importantes. En este artículo presentamos un enfoque alternativo para sinte­tizar PI de forma y tamaño impresionante.

Carbon nanotubes (CNT) provide an outstanding property spectrum which can be used to improve a wide range of materials. However, the transfer of properties from the nanoscale to a macroscopic material is a limiting factor. Different approaches of functionalizing the surface of a CNT can improve the interaction with the surrounding matrix but is connected to difficult and expensive treatments, which are usually inconvenient for industrial applications. Here, a simple and eco-friendly method is presented for the oxidation of CNT, where hydrogen peroxide (H2O2) is the only chemical needed and no toxic emissions are released. Also, the extensive step of the incorporation of CNT to an epoxy matrix is simplified to an ultrasonic dispersion in the liquid hardener component. The effectiveness is proven by mechanical tests of produced CNT/CFRP and compared to a conventional processing route. The combination of those simple and cost efficient strategies can be utilized to produce multiscale composites with improved mechanical performance in an ecological and economical way.

‘Extreme biomimetics’ and ‘geomimetics’ are relatively recent fields of materials chemistry. Both take inspiration from natural materials for generating novel synthetic materials or enhanced properties in known materials. In geomimetics, the source of inspiration is geological systems, while extreme biomimetics is motivated by organisms operating in—from an anthropocentric point of view—extreme conditions. This review article focuses on geomimetic and extreme biomimetic hydrothermal synthesis. Since hydrothermal preparative chemistry typically uses nothing but water and the required precursors, the field belongs to the research area of ‘green materials chemistry’. Geomimetics, on the one hand, takes inspiration from natural materials formation. Extreme Biomimetics, on the other hand, is inspired by materials found in extremophile organisms, instead of aiming to implement their actual biosynthesis. In this contribution, both extreme biomimetics and geomimetics are first defined, and further critically discussed on the basis of recent, selected examples. Moreover, the necessity for the two closely related fields as well their prospects are commented on.