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Metal fabrication workshops (MFWs) are common businesses in Ugandan cities, and especially those producing metallic security gates, window and door frames (burglar-proof), and balcony and staircase rails. The objective of this study was to comparatively assess the pollution levels and potential health risks of manganese (Mn), chromium (Cr), cadmium (Cd), lead (Pd) and nickel (Ni) in pooled surface soil samples from four 5-, 7-, 8-, and 10-year-old MFWs (n = 28) and a control site (n = 8) in Mbarara City, Uganda. The concentration of the potentially toxic elements (PTEs) was determined using inductively coupled plasma–optical emission spectrometry. Contamination, ecological, and human health risk assessment indices and models were used to identify any risks that the PTEs could pose to the pristine environment and humans. Our results showed that PTE pollution of soils is occuring in the MFWs than at the control site. The mean concentrations of the PTEs (mg kg−1) in the samples were: Mn (2012.75 ± 0.23–3377.14 ± 0.31), Cr (237.55 ± 0.29–424.93 ± 0.31), Cd (0.73 ± 0.13–1.29 ± 0.02), Pb (107.80 ± 0.23–262.01 ± 0.19), and Ni (74.85 ± 0.25–211.37 ± 0.14). These results indicate that the PTEs could plausibly derive from the fabrication activities in these workshops, which is supported by the high values of contamination factors, index of geoaccumulation, and the overall increase in pollution load indices with the number of years of operation of the MFWs. Human health risk assessment showed that there are non-carcinogenic health risks that could be experienced by children who ingest PTEs in the soils from the 7-, 8- and 10-year-old MFWs. The incremental life cancer risk assessment suggested that there are potential cancerous health effects of Cd and Ni that could be experienced in children (who ingest soils from all the four MFWs) and adults (ingesting soils from the 8- and 10-year-old MFWs). This study underscores the need to implement regulatory guidelines on the operation and location of MFWs in Uganda. Further research should be undertaken to investigate the emission of the PTEs during welding operations in the MFWs.

Two new heteroleptic cobalt(III)dialkyldithiophosphate complex cations with a 1,2-bis(diphenylphosphino)ethane (dppe) ancillary ligand having formula [Co{S2P(OR)2}2(dppe)](B(C6H5)4) (R = –C2H5 (Co–Et); –CH(CH3)2 (Co–Pr)) have been synthesized and characterized spectroscopically as well as via single crystal X-ray diffraction analysis. The single crystal X-ray diffraction analyses reveal that the immediate geometries around Co(III) in both complexes are distorted octahedral, which are satisfied by four sulfur atoms of two dialkyldithiophosphate ligands and two phosphorus centers of the dppe ligand. These complex cations are neutralized by tetraphenyl borate B(C6H5)4 anions. The solid-state framework of both complexes are stabilized by C–H⋯π and C–H⋯C interactions. The nature of these interactions have been addressed with the help of Hirshfeld surface analysis, and percent contributions of pertinent interactions in the crystal structure of these complexes have been addressed using fingerprint plots. Both complexes have been used as heterogeneous electrocatalysts for the oxygen evolution reaction (OER). Results suggest that Co–Et is a better electrocatalyst for the OER, displaying an onset potential of 1.68 V and Tafel slope of 114 mV dec−1. Furthermore, in the homogeneous electrocatalysis of the hydrogen evolution reaction (HER) using trifluoroacetic acid, the overpotential for Co–Et and Co–Pr have been 1.05 V and 0.92 V, respectively, with turnover frequencies of 1518 s−1 and 287.5 s−1, respectively. Overall, heterogeneous OER and homogenous HER results suggest that Co–Et can be used as an efficient molecular electrocatalyst for oxygen/hydrogen evolution reactions. [ABSTRACT FROM AUTHOR]

In this work, a new d10-configuration based Cd(II) coordination polymer (CP) with the formula [Cd2(CH3COO)2(bimb)2]·2ClO4 (1) have been synthesized using 4,4′-bis(imidazolyl)biphenyl (bimb) ligand and characterized. Single-crystal X-ray analysis reveals that the CP forms a 2D layer connected to a 3D supramolecular framework with weak packing interactions between benzyl and imidazolyl rings. CP 1 has been used as a photoluminescent sensor and a photocatalyst for the photodegradation of antibiotics, in particular nitrofurantoin (NFT). Sensing experiments indicate that 1 can selectively detect nitrofurantoin with a limit of detection of 0.025 μM, whereas when employed as a photocatalyst, CP 1 can photodecompose NFT up to 91.83% in a time span of 20 min. The decline in the photoluminescence intensity of CP 1 in the presence of NFT and the photocatalytic mechanism are addressed using theoretical calculations. [ABSTRACT FROM AUTHOR]