A comprehensive study investigated the effect of polar protic (methanol and water) and polar aprotic (acetonitrile and acetone) solvents on the chromatographic separation and negative-ion electrospray (ESI) response of 49 diverse small, acidic molecules. Flow injection experiments on a triple quadrupole were used to measure the response in neat solvents after optimization of source conditions and implementation of a rigorous quality control program (the later ensured that changes in analyte response were due to the analyte/solvent measured and not changes in instrument performance over time). In all solvents, compounds with electron-withdrawing groups and extended conjugation ionized best due to resonance and inductive effects. Ionization was greatest in methanol or water for all compounds that elicited a response, thus revealing that enhanced sensitivity and lower limits of detection are achieved with polar protic solvents. Response in acetone was equal to or slightly lower than response in acetonitrile in flow injection experiments; however, the water/acetonitrile and water/acetone mobile phases produced the better chromatographic separation. Water/methanol produced slightly less satisfactory separation but the greatest overall response. This increase in response was attributed to the protic nature of methanol and the elution of compounds in a higher organic mobile phase composition (retention times were ∼30% later in methanol). This work is intended to facilitate rational liquid chromatography/mass spectrometry method development for small molecule applications, including metabolomics.
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http://dx.doi.org/10.1021/ac302397b | DOI Listing |
Photochem Photobiol Sci
January 2025
CQC-IMS, Department of Chemistry, University of Coimbra, 3004-535, Coimbra, Portugal.
Solvatochromism exhibited by azobenzene-4-sulfonyl chloride (here abbreviated as Azo-SCl) has been investigated in a series of non-polar, polar-aprotic and polar-protic solvents. The UV-vis spectra of Azo-SCl exhibit two long-wavelength bands, observed at 321-330 nm (band-I) and 435-461 nm (band-II), which are ascribed to the π*-π (S ← S) and π*-n (S ← S) transitions, respectively. The shorter wavelength band indicates a reversal in solvatochromism, from negative to positive solvatochromism, for a solvent with a dielectric constant of 32.
View Article and Find Full Text PDFChem Asian J
January 2025
Technische Universität Braunschweig, Institute of Medicinal and Pharmaceutical Chemistry, Beethovenstr. 55, 38106, Braunschweig, GERMANY.
Silver N-heterocyclic carbene (NHC) complexes are known to form biscarbene species from monocarbene analogs in protic polar solvents. However, the effect of the respective species of silver NHC complexes on their biological activity against bacteria or cancer cells has not been systematically explored, either in vitro or in vivo. The direct and simple conversion of monocarbene silver N-heterocyclic carbene (NHC) halide complexes (NHC)AgX, (X= Cl, Br) 1a/b - 5a/b to their biscarbene analogues (NHC)2AgX 1c/d - 5c/d is reported.
View Article and Find Full Text PDFDalton Trans
January 2025
Department of Chemistry, Birla Institute of Technology and Science Pilani, Hyderabad, 500078, India.
Flexible bis-benzimidazole-based V-shaped amphiphilic probes (1 and 2) that form a fluorescent nanoscopic assembly in aqueous media have been designed. The ion-binding properties of compound 1 are investigated in both polar protic (water) and aprotic (acetonitrile) solvents. In acetonitrile, the compound shows a distinct chromogenic response towards Hg (LOD: 8.
View Article and Find Full Text PDFJ Chromatogr A
December 2024
HUN-REN Molecular Interactions in Separation Science Research Group, Ifjúság útja 6, H-7624 Pécs, Hungary; Department of Analytical and Environmental Chemistry and Szentágothai Research Center, University of Pécs, Ifjúság útja 6, H-7624 Pécs, Hungary; Institute of Bioanalysis, Medical Scool, University of Pécs, Szigeti út, H-7624 Pécs, Hungary. Electronic address:
Non-destructive chromatographic methods were used to determine the hold-up volumes of four self-packed columns containing embedded phosphate groups. The stationary phases are named Diol-P-C10, Diol-P-C18, Diol-P-Benzyl and Diol-P-Chol. The hydrophobicity of organic ligands bound to the phosphate group increases in the benzyl< decyl < octadecyl
Phytochem Anal
December 2024
Department of Chemistry, Colorado State University, Fort Collins, Colorado, USA.
Introduction: Phenolic compounds garner interest in developing medicines, nutraceuticals, and cosmeceuticals based on natural products. The quantity of phenolic compounds in a sample is commonly determined via spectrophotometry; however, this instrumented technique is relatively laborious and time consuming and requires a large amount of reagents.
Objective: This work aimed to develop a simple, point-of-need colorimetric sensor to rapidly determine total phenolic content (TPC) in tea extracts.
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