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https://www.selleckchem.com/products/PP242.html Conjugated microporous polymers (CMPs) with uniform morphology have shown fascinating application in the separation science. In this study, metal-free Knoevenagel condensation was adopted to prepare spherical sp2 carbon-conjugated microporous polymers, which used tetrakis(4-formylphenyl)methane and 1,4-phenylenediacetonitrile as monomers. Due to the remarkable extraction capability for carbamate pesticides (CPs), the as-synthesized CMPs were fabricated as the coating for solid-phase microextraction (SPME). After optimized SPME parameters (adsorption time, salt concentration, sample pH, adsorption temperature, desorption time, desorption solvent and desorption volume), ten CPs in water samples were quantified by ultrahigh performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS). Linearity in the range 0.005-100 ng mL-1 with low detection limits of 0.00060-0.017 ng mL-1 was obtained. The intra-day and inter-day precisions expressed as relative standard deviations were 1.5-8.1% and 1.1-8.0%, respectively. Fiber-to-fiber reproducibility was below 7.3%. The CMPs-SPME-UPLC-MS/MS method was applied to detect trace CPs in real water samples with relative recoveries from 91.8% to 108%.The enantiomeric determination of chiral drugs in the environment is of emerging concern since their enantiomers often exhibit stereoselectivity in environmental occurrence, fate and toxicity. In this study a method based on solid-phase extraction followed by chiral liquid chromatography and high-resolution mass spectrometry has been developed for the enantiomeric determination of a group of cathinones in river water and effluent wastewater. The enantioseparation was carried out using a Chiralpak CBH column in reversed-phase mode, and optimised by evaluating the effects of flow rate, buffer concentration and organic modifier. Under optimal conditions, good enantioseparations (Rs ≥1.2) were achieved for all the analytes. Two mixed-mo

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