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Self-organizing macrocyclic receptor-sensors for phosphorus oxyanions, phosphates, and phosphonates comprising imine moieties were prepared by condensation of dipyrrolylmethane dicarbaldehyde with diethylene triamine. The incorporation of flexible ethylene moieties endows the macrocycle with unprecedented flexibility and ability to accommodate numerous phosphorus oxyanions from orthophosphate to large anions such as ATP or phosphonate glyphosate. The anion binding was elucidated by NMR titrations, low-temperature NMR, and NOESY NMR. The incorporation of dansyl fluorophore enables sensing of anions using the fluorescence signal, whereas the changes in fluorescence intensity, width of the fluorescence band, and position of the maxima are analyte-specific and useful in recognition and identification of eleven different P-oxyanions in water. The affinity (K) for Na salts was HPO ≈ Methylphosphonate > HPO > Phenylphosphonate > Glyphosate > AMP > ADP > ATP. Interestingly, phosphonates, including methylphosphonate and glyphosate anions, were also found to display a strong affinity (K ∼10 M) while halides, nitrate, carbonates, or hydrogen sulfate did not show a significant affinity. The determined fluorescence spectral parameters were used to classify the 12 analytes (11 anions and water) using Linear Discriminant Analysis (LDA). Quantification was performed using LDA and Support Vector Machine (SVM), and the phosphonate concentrations in unknown samples were determined with an error of 3.5% or lower.
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http://dx.doi.org/10.1002/chem.202501700 | DOI Listing |
Chemistry
August 2025
Chemistry Department, Bowling Green State University, Bowling Green, Ohio, 43403, USA.
Self-organizing macrocyclic receptor-sensors for phosphorus oxyanions, phosphates, and phosphonates comprising imine moieties were prepared by condensation of dipyrrolylmethane dicarbaldehyde with diethylene triamine. The incorporation of flexible ethylene moieties endows the macrocycle with unprecedented flexibility and ability to accommodate numerous phosphorus oxyanions from orthophosphate to large anions such as ATP or phosphonate glyphosate. The anion binding was elucidated by NMR titrations, low-temperature NMR, and NOESY NMR.
View Article and Find Full Text PDFWater Res
August 2025
Ministry of Environment, Misagangbyeonhangang-ro 229, Hanam-si, Gyeonggi-do 12902, South Korea. Electronic address:
Anisotropic goethite nanoparticles play a critical role in the environmental behavior of nutrient and contaminant due to their abundance, high surface area, and strong binding affinity; however, their transformation into smaller, more mobile nanocolloids under natural setting remains underexplored. Here, we show that natural wet-dry cycles at alkaline pH in the presence of As(V) or P(V) induce extensive goethite nanorod (GtNR) fragmentation into nanospheres (GtNS) and the formation of ferrihydrite single-digit nanospheres (FhSDNS), driven by drying-induced surface reactions, oxyanion-mediated dissolution, reprecipitation, passivation, capillary stress, and defect sites. Under identical conditions, nanospheres of hematite, maghemite, and magnetite exhibit minimal transformation, underscoring the unique susceptibility of GtNR.
View Article and Find Full Text PDFSci Total Environ
August 2025
College of Natural Resources & Environment, South China Agricultural University, Guangzhou 510642, China.
In natural ecosystems, the (bio)availability of arsenic and phosphorus is greatly controlled by their interactions with metal (hydr)oxides and organic matter. Humic substances (HS), encompassing humic acids (HA) and fulvic acids (FA), constitute the primary form of organic matter. In this study, batch adsorption experiments were conducted and integrated with the NOM-CD model to achieve a molecular-level understanding of HS on the competitive interactions among arsenite, arsenate, and phosphate on goethite surfaces.
View Article and Find Full Text PDFAnal Chim Acta
November 2024
School of Civil Engineering, Yancheng Institute of Technology, Yancheng, Jiangsu, 224007, PR China.
Environ Res
February 2024
University of Manchester, Department of Earth and Environmental Sciences, Geomicrobiology Group, Williamson Building, M13 9QQ, Oxford Road, Manchester, UK. Electronic address:
Vivianite (Fe(PO)·8HO), a sink for phosphorus, is a key mineralization product formed during the microbial reduction of phosphate-containing Fe(III) minerals in natural systems, and also in wastewater treatment where Fe(III)-minerals are used to remove phosphate. As biovivianite is a potentially useful Fe and P fertiliser, there is much interest in harnessing microbial biovivianite synthesis for circular economy applications. In this study, we investigated the factors that influence the formation of microbially-synthesized vivianite (biovivianite) under laboratory batch systems including the presence and absence of phosphate and electron shuttle, the buffer system, pH, and the type of Fe(III)-reducing bacteria (comparing Geobacter sulfurreducens and Shewanella putrefaciens).
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