Tannins, an abundant group of plant secondary compounds, raise interest in different fields of science, owing to their unique chemical characteristics. In chemical ecology, tannins play a crucial role in plant defense against pathogens, herbivores, and changing environmental conditions. In the food industry and in medicine, tannins are important because of their proven positive effect on human health and disease treatment. Such wide interests fueled studies on tannin chemistry, especially on their flagship ability to precipitate proteins. In this Review, we expand the basic knowledge on tannin chemistry to the newest insights from the field. We focus especially on tannin reactions with different non‐protein organic N compounds, as well as the complex interactions of tannins with enzymes, resulting in either an increase or decrease in enzyme activity.
Based on their rigid-rod structure all-conjugated, rod-rod block copolymers show a preferred tendency to self-assemble into low-curvature vesicular or lamellar nanostructures independent from their specific chemical structure and composition. This unique and attractive behaviour is clearly illustrated in a few examples of such all-conjugated block copolymers. The resulting nanostructured heteromaterials may find applications in electronic devices or artificial membranes.
Novel, all-conjugated polyelectrolyte block copolymers of the rod-rod type can be generated in a ''grafting from'' scheme and exhibit a preferred tendency to self-assemble into layered aggregates both in solution and the solid state. Here, the rigid-rod structure of the individual, complex macromolecules favours the formation of low-curvature vesicular and lamellar aggregates. Our poly(9,9-dialkylfluorene)-b-poly [3-(6-ammoniumhexyl)thiophene] (PF2/6-b-P3TMAHT and PFO-b-P3TMAHT, where PF2/6 and PFO denote 2-(ethyl)hexyl and linear octyl alkyl pendant groups, respectively), and poly(9,9-dialkylfluorene)-b-poly[3-(6-pyridylhexyl)thiophene] (PF2/6-b-P3PyHT and PFO-b-P3PyHT) polyelectrolyte diblock copolymers allow for simple and reliable control of the occurring self-organisation process and the resulting nano-scaled architectures. They are, therefore, promising candidates for application as the active layer in electronic devices or as functional membranes (e.g. for sensor applications). Moreover, the electronic properties of the materials (especially the excitation energy transfer between both blocks) strongly depend on the aggregation state present. Aggregation can be further controlled via addition of oppositely charged surfactants resulting in the formation of ordered polyelectrolyte/surfactant complexes.
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