Phosphorus dendrimer immobilized azabis(oxazoline) ligands can be efficiently synthesized up to the third generation with 48 ligand molecules being attached to the periphery using click chemistry. The so-assembled macromolecules were evaluated in copper(II)-catalyzed asymmetric benzoylations, showing good yields and enantioselectivities. Moreover, the copper(II)-catalysts could be readily recovered and reused in several cycles. The globular structure of the dendritic ligands seems to prevent interference of the triazole moieties in the catalysis, contrasting MeOPEG or polystyrene bound ligands of the same type.

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The attachment of multiple triazole moieties and perfluoroalkyl chains to TEMPO promotes emulsion formation in dichloromethane/water, giving a highly active and easily recoverable catalyst for the oxidation of alcohols.

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Keratin, obtained from chicken feathers, was grafted on the surface of commercially available carbon nanotubes. The original procedure developed allows a covalent interaction between some specific chemical groups characteristic of the keratin, with some functional groups introduced on purpose on the surface of the nanotubes, as revealed by infrared and Raman spectroscopies, which also allowed to determine structural changes introduced during the process, such as crystallinity, which lead to changes in other properties, as well.

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Inclusion compounds formed between sertraline stereoisomers and β-cyclodextrin, and 2-hydroxypropyl-β-cyclodextrin, were analyzed by using quantum chemistry methods.