Chlorophyllides: Preparation, Purification and Application

Chlorophyllides can be found in photosynthetic organisms. Generally, chlorophyllides have a-, b-, c-, d-, and f-type derivatives, and all chlorophyllides have a tetrapyrrole structure with a Mg ion at the center and a fifth isocyclic pentanone. Chlorophyllide a can be synthesized from protochlorophyllide a, divinyl chlorophyllide a, or chlorophyll. In addition, chlorophyllide a can be transformed into chlorophyllide b, chlorophyllide d, or chlorophyllide f. Chlorophyllide c can be synthesized from protochlorophyllide a or divinyl protochlorophyllide a. Chlorophyllides have been extensively used in food, medicine, and pharmaceutical applications. Furthermore, chlorophyllides exhibit many biological activities, such as anti-growth, antimicrobial, antiviral, antipathogenic, and antiproliferative activity. The photosensitivity of chlorophyllides that is applied in mercury electrodes and sensors were discussed. This article is the first detailed review dedicated specifically to chlorophyllides. Thus, this review aims to describe the definition of chlorophyllides, biosynthetic routes of chlorophyllides, purification of chlorophyllides, and applications of chlorophyllides.

The effects of the chemical environment of menaquinones in lipid monolayers on mercury electrodes on the thermodynamics and kinetics of their electrochemistry

The effects of the chemical environment of menaquinones (all-trans MK-4 and all-trans MK-7) incorporated in lipid monolayers on mercury electrodes have been studied with respect to the thermodynamics and kinetics of their electrochemistry. The chemical environment relates to the composition of lipid films as well as the adjacent aqueous phase. It could be shown that the addition of all-trans MK-4 to TMCL does not change the phase transition temperatures of TMCL. In case of DMPC monolayers, the presence of cholesterol has no effect on the thermodynamics (formal redox potentials) of all-trans MK-7, but the kinetics are affected. Addition of an inert electrolyte (sodium perchlorate; change of ionic strength) to the aqueous phase shifts the redox potentials of all-trans MK-7 only slightly. The formal redox potentials of all-trans MK-4 were determined in TMCL and nCL monolayers and found to be higher in nCL monolayers than in TMCL monolayers. The apparent electron transfer rate constants, transfer coefficients and activation energies of all-trans MK-4 in cardiolipins have been also determined. Most surprisingly, the apparent electron transfer rate constants of all-trans MK-4 exhibit an opposite pH dependence for TMCL and nCL films: the rate constants increase in TMCL films with increasing pH, but in nCL films they increase with decreasing pH. This study is a contribution to understand environmental effects on the redox properties of membrane bond redox systems. Graphical abstract

Application of Hierarchical Nanostructured WO3 and Fe2O3 Composites for Photodegradation of Surfactants in Water Samples

This study describes the utilization of hierarchical photoactive surface films for the decomposition of surfactants in water samples (with different pH). Photoactive films, containing tungsten (VI) oxide and iron (III) oxide (hematite), were deposited in a systematic and controlled manner using a layer-by-layer method. Physicochemical properties of the photoactive materials were developed and characterized using XRD analysis, Raman spectroscopy, water contact angle, voltammetry, and microscopic (SEM) techniques. The resulting multilayer films showed attractive performances in the photodegradation of the anionic surfactant sodium dodecyl sulfate (SDS) and the nonionic surfactant (1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol (Triton™ X-144) under solar light irradiation. The efficiency of the surfactants’ photodegradation was evaluated with a “test” based on a method, which is extremely sensitive to surfactants’ interference, with trace analysis of Pb using anodic stripping voltammetry on mercury electrodes (recovery study). The usefulness of hierarchical photoactive systems in the photodegradation of both surfactants is demonstrated in the presence and absence of the applied bias voltage. The maximum decomposition times were 2–3 h and 30 min, respectively. Furthermore, a properly designed layer system may be proposed, matching the pH of the water sample (depending on the treatment on the sampling side).

Redox Properties of Mononuclear Dicarbonyl and Carbonylphosphine Rhodium (I) Complexes Containing β-diketonate Ligands

The redox properties of mononuclear dicarbonyl and carbonylphosphine rhodium (I) complexes (CO)(L)Rh(RC(O)CHC(O)R’) with chelate β-diketonate ligands (L = CO, PPh3; R, R’ = Me, Ph; CF3, C4H3S) were studied by electrochemical methods at platinum, glassed carbon and dropping mercury electrodes in acetonitrile. Schemes of their redox reactions were established

Recent Applications of Silver Amalgam Electrodes for Analysis of Pharmaceuticals and Vitamins

The features and applications of silver amalgam electrodes in electroanalysis of pharmaceuticals and vitamins are summarized in this review. The state-of-the-art in the preparation and construction of solid silver amalgam electrodes for prolonged and userfriendly use is presented. Although not as widely spread as other electrode materials, silver amalgam possesses a unique and viable combination of favorable electrochemical properties, which are close to ideal mercury electrodes, non-toxic character, high durability and mechanical stability, if properly prepared. Its capability of conducting the redox processes at highly negative potentials is essential for the analysis of large number of bioactive organic compounds. The review features also overview information for each application in drug or vitamin analysis divided to the sections according to the construction variants of silver amalgam electrodes.