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An integrated method of dynamic extraction of perchloroethylene (PCE) with polydimethylsiloxane (PDMS) helical solid sorbent followed by injection into a gas chromatograph was developed for the determination of the real concentration of PCE in groundwater before and after its degradation by oxidation with KMnO(4). The main parameters (agitation, temperature, salts, pH) that affect the extraction efficiency have been evaluated and optimized. The increase of the extracted amount of PCE due to the presence of the salts could be partially compensated by the opposite effect of the insoluble MnO(2), and of the presence of HCl and the global effect of the matrix would be less important for the reproducibility of the PCE extraction. The quantitative analysis of PCE was carried out with the external standard method using the calibration-curve technique. The limit of detection for PCE was found of 0.05 mg L(-1) using flame ionization detector. The solubility of PCE in water was studied by extraction of PCE with PDMS helical solid sorbent from standard solution with different amounts of PCE added into the same volume of water and was found to decrease with settling time, because the fine droplets created during the agitation of the mixture were slowly merged in drops on the bottle walls and were not transferred into the extraction vial for GC analysis. The limit of solubility was evaluated using a graphical method and was estimated at 224.2+/-15.7 mg L(-1) of PCE in water at 25 degrees C.
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http://dx.doi.org/10.1016/j.chemosphere.2009.02.016 | DOI Listing |
Org Lett
September 2025
Max Planck Institute of Microstructure Physics, Weinberg 2, 06120 Halle, Germany.
Helical nanographenes (NGs) play a crucial role in the development of chiral nanomaterials due to their distinctive optoelectronic and chiroptical properties. Herein, we report the efficient synthesis of two unprecedented azulene-embedded asymmetric triple helical NGs ( and ) with controllable helicene subunit lengths and π-extension. The crystallographic analysis confirms their highly twisted and asymmetric geometries.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
September 2025
Departament de Química Inorgànica i Orgànica, Universitat de Barcelona, Diagonal 645, Barcelona, 08028, Spain.
Spins within molecules benefit from the atomistic control of synthetic chemistry for the realization of qubits. One advantage is that the quantum superpositions of the spin states encoding the qubit can be coherently manipulated using electromagnetic radiation. The main challenge is the fragility of these superpositions when qubits are to partake of solid-state devices.
View Article and Find Full Text PDFBiochim Biophys Acta Biomembr
August 2025
University of Strasbourg / CNRS, UMR7177, Chemistry Institute, 67000 Strasbourg, France; Institut Universitaire de France, 75005 Paris, France. Electronic address:
Collagen VI is an extracellular matrix protein forming complex microfibrillar networks in connective tissues. Specifically, we focused on its role in innate immunity, in particular on cationic sequence motifs from the α3(VI)-chain, which exhibit strong antibacterial properties against both Gram-positive and Gram-negative bacteria in vitro and in vivo. Cytotoxicity assays revealed minimal to no adverse effects, even at concentrations effective against bacterial pathogens.
View Article and Find Full Text PDFInt J Mol Sci
August 2025
Vavilov Institute of General Genetics RAS, 119333 Moscow, Russia.
Antimicrobial peptides (AMPs) are the promising candidates for the development of next-generation antimicrobials for agriculture and medicine; however, their large-scale production is costly. The γ-core motif peptides, functionally significant fragments of AMPs responsible for the antimicrobial activity, provide a more economical and feasible approach for the commercial development of novel antimicrobials. In the present work, we undertook a comprehensive study of antimicrobial properties of several γ-core peptides derived from defensins and snakins of , a medicinal plant known for its valuable pharmacological properties.
View Article and Find Full Text PDFAcc Chem Res
August 2025
Laboratory of Catalysis and Organic Synthesis, Ecole Polytechnique Fédérale de Lausanne, EPFL SB ISIC LCSO, BCH 4306, 1015 Lausanne, Switzerland.
ConspectusAlkynes are one of the most fundamental functional groups in organic synthesis due to the versatile chemistry of the triple bond, their unique rigid structure, and their use in bioconjugation. The introduction of alkynes onto organic molecules traditionally relies on nucleophilic activation, often requiring strong bases or metal catalysts. These conditions, however, restrict applications involving biomolecules such as peptides and proteins due to functional group incompatibility.
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