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Natural carboxylic acids are plant-derived compounds that are known to possess biological activity. The aim of this review was to compare the effect of structural differences of the selected carboxylic acids (benzoic acid (BA), cinnamic acid (CinA), p-coumaric acid (p-CA), caffeic acid (CFA), rosmarinic acid (RA), and chicoric acid (ChA)) on the antioxidant, antimicrobial, and cytotoxic activity. The studied compounds were arranged in a logic sequence of increasing number of hydroxyl groups and conjugated bonds in order to investigate the correlations between the structure and bioactivity. A review of the literature revealed that RA exhibited the highest antioxidant activity and this property decreased in the following order: RA > CFA ~ ChA > p-CA > CinA > BA. In the case of antimicrobial properties, structure-activity relationships were not easy to observe as they depended on the microbial strain and the experimental conditions. The highest antimicrobial activity was found for CFA and CinA, while the lowest for RA. Taking into account anti-cancer properties of studied NCA, it seems that the presence of hydroxyl groups had an influence on intermolecular interactions and the cytotoxic potential of the molecules, whereas the carboxyl group participated in the chelation of endogenous transition metal ions.

The anthropogenic cycle of Pd in the environment, its fate and impact is still unknown due to limitations of measurement techniques. For separation and pre-concentration of Pd(II) ions, mesoporous silica materials MCM-41 were synthesized and functionalized with different amounts of 3-mercaptopropyltrimethoxysilane (MPTMS) by co-condensation and grafting methods. The structural and textural properties of materials were characterized using XRD, TEM, SEM and BET techniques. The results proved that functionalization with thiol groups did not significantly affect structural and textural parameters of synthesized sorbents. The Pd(II) ions were quantitatively retained on sorbents functionalized by grafting in acidic solutions (pH 2), efficiently eluted with 0.1 mol L−1 thiourea solution in 1 mol L−1 HCl and determined by electrothermal atomic absorption spectrometry (ETAAS). The limit of detection (LOD) of the developed SPE ETAAS method was 0.06 ng mL−1, and the pre-concentration factor was 30. For analysis of Pd in environmental water samples inductively coupled plasma mass spectrometry (ICP-MS) in MS/MS mode was used. Spectral interferences on 105Pd caused by the presence of Sr in water samples were eliminated using helium (5 mL min−1) or ammonia (7 mL min−1) gas in collision/reaction cell. The developed SPE ICP-MS method is characterized by good selectivity in the presence of interfering elements and chloride ions and detection limit of 0.0002 ng mL−1. Its accuracy was confirmed by analysis of spiked water samples. The application of ICP-MS together with efficient separation/pre-concentration of analyte on thiol-functionalized MCM-41 sorbents allows to determine Pd in environmental water samples at pg mL−1 level.