Fourier transform infrared (FT-IR) attenuated total reflection (ATR) spectroscopy was used to discriminate five commonly encountered soil-borne fungi that cause severe economic damage to agriculture: Colletotrichum, Fusarium, Pythium, Rhizoctonia, and Verticillium. Contrary to previous studies related to microorganism discrimination using FT-IR-ATR spectroscopy, the pathogen samples were not dried on the ATR crystal, which is a time-consuming operation. Rather, after removing some pathogen filaments from the solution using tweezers, these were placed directly on a flat ATR crystal and pressure was applied using a pressure clamp. Following water subtraction, baseline correction, and normalization of the spectra, principal component analysis was used as a data-reduction step and canonical variate analysis was used for discrimination. Discrimination was performed at the genus level and at the strain level for Colletotrichum. For discrimination between the five fungi at the genus level, the success rate for the validation samples ranged from 75% to 89%. For discrimination between the two Colletotrichum strains, the success rate was 78%. Comparison with spectra of similar fungi dried on the ATR crystal showed that both types of spectra were very similar, indicating that drying the samples on the ATR crystal is not required and can be replaced by mathematical post-processing of the spectra. For routine analyses that involve rapid screening of very large amounts of samples, this approach allows for increasing significantly the number of samples that can be analyzed daily.
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http://dx.doi.org/10.1366/000370208783759678 | DOI Listing |
Soft Matter
January 2025
School of Chemistry and University of Sydney Nano Institute, The University of Sydney, Sydney, NSW, 2006, Australia.
Self-assembly of amphiphilic molecules can take place in extremely concentrated salt solutions, such as inorganic molten salt hydrates or hydrous melts. The intermolecular interactions governing the organization of amphiphilic molecules under such extreme conditions are not yet fully understood. In this study, we investigated the specific effects of ions on the self-assembly of the non-ionic surfactant CH(OCHCH)OH (CE) under extreme salt concentrations, using calcium nitrate tetrahydrate as a reference.
View Article and Find Full Text PDFInt J Biol Macromol
January 2025
Faculty of Polymer Engineering and Color Technology, Amirkabir University of Technology, Tehran, Iran.
In this research, tartaric acid was used to enhance the hydroxyapatite coating on AZ31 Mg alloy substrate through post-treatment and direct addition methods, and the corrosion resistance and biological activity of the samples were investigated. The parameters of concentration, immersion time, and pH of the coating solution were optimized by Electrochemical Impedance Spectroscopy (EIS) and Direct Current (DC) Polarization techniques. According to EIS results in the post-treatment method, tartaric acid with a concentration of 1 g/L, pH = 9 and immersion time of 2 min, increased the corrosion resistance of hydroxyapatite coating from 3630 to about 18,763 Ω.
View Article and Find Full Text PDFMolecules
December 2024
Ruđer Bošković Institute, Bijenička Cesta 54, 10000 Zagreb, Croatia.
This study examines the influence of ligand design on the structural, optical, and electrical properties of copper-based coordination complexes. Ligands HL and HL were synthesized via the reaction of 5-nitrosalicylaldehyde with 2-hydroxy- or 4-hydroxybenzhydrazide. HL was obtained from the reaction of carbohydrazide and salicylaldehyde, while HL was prepared by condensing 4-methoxysalicylaldehyde with thiocarbohydrazide.
View Article and Find Full Text PDFMolecules
December 2024
Laboratory of Chemistry and Technology of Polymers and Colors, Department of Chemistry, Aristotle University of Thessaloniki, GR-54124 Thessaloniki, Greece.
This study presents the synthesis and characterization of a series of multiblock copolymers, poly(ethylene 2,5-furandicarboxylate)-poly(ε-caprolactone) (PEF-PCL), created through a combination of the two-step melt polycondensation method and ring opening polymerization, as sustainable alternatives to fossil-based plastics. The structural confirmation of these block copolymers was achieved through Attenuated Total Reflectance Fourier Transform Infrared Spectroscopy (ATR-FTIR), ensuring the successful integration of PEF and PCL segments. X-ray Photoelectron Spectroscopy (XPS) was employed for chemical bonding and quantitative analysis, providing insights into the distribution and compatibility of the copolymer components.
View Article and Find Full Text PDFChem Sci
January 2025
Frontier Institute of Science and Technology, State Key Laboratory of Electrical Insulation and Power Equipment, MOE Key Laboratory for Nonequilibrium Synthesis of Condensed Matter, Xi'an Key Laboratory of Electronic Devices and Materials Chemistry and School of Chemistry, Xi'an Jiaotong University 99 Yanxiang Road Xi'an Shaanxi 710054 P. R. China
The benzene tetraanion-bridged rare earth inverse arene amidinate complexes [{Ln(κ:η-Piso)}(μ-η:η-CH)] (2-Ln, Ln = Gd, Tb, Dy, Y; Piso = {(NDipp)C Bu}, Dipp = CH Pr-2,6) were prepared by the reduction of parent Ln(iii) bis-amidinate halide precursors [Ln(Piso)X] (Ln = Tb, Dy; X = Cl, I) or [Ln(Piso)I] (Ln = Gd, Y) with 3 eq. KC in benzene, or by the reaction of the homoleptic Ln(ii) complexes [Ln(Piso)] (Ln = Tb, Dy) with 2 eq. KC in benzene.
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