The effect of counter anions on thermally induced manganese(iii)-based SCO within the [Mn(5-F-sal-N-1,5,8,12)]Y family has been investigated. All the complexes are crystallized without any lattice solvents. Crystal packing and intermolecular forces influence the spin-state stabilization and spin-transition profiles. Magnetic measurements indicate that salts with octahedral anions, [Mn(5-F-sal-N-1,5,8,12)]PF6 (1), [Mn(5-F-sal-N-1,5,8,12)]AsF6 (2) and [Mn(5-F-sal-N-1,5,8,12)]SbF6 (3), show HS electronic configurations between 2 and 300 K, and there exist π-π stackings between the phenyl groups from the neighboring [Mn(5-F-sal-N-1,5,8,12)]+ cations. As for the tetrahedral anions, complex [Mn(5-F-sal-N-1,5,8,12)]BF4 (4) exhibits a gradual and incomplete spin conversion. Complex [Mn(5-F-sal-N-1,5,8,12)] ClO4 (5) shows a nearly complete SCO with T1/2 = 100 K. The remaining salts with spherical anions form Nam-HX (X = Cl, Br, I) hydrogen bonds between Mn(iii) cations and counterions. Complexes [Mn(5-F-sal-N-1,5,8,12)]Cl (6) and [Mn(5-F-sal-N-1,5,8,12)] Cl0.28Br0.72 (7) feature gradual SCO behaviors with T1/2 = 220 K and 235 K, respectively. Complex [Mn(5-F-sal-N-1,5,8,12)]I (8) exhibits a more gradual spin conversion and is far from a complete HS state with a χMT value of 1.89 cm3 mol-1 K at 400 K.Ion-specific effects of cations (Li+, Na+, K+, Mg2+, Ca2+) and anions (F-, Cl-) on the hydrogen bond structure and dynamics of the coordination waters in the hydration shells have been studied using molecular dynamics simulations. Our simulations indicate that the hydrogen bonds between the first and second hydration shell waters show binary structural and dynamic properties. The hydrogen bond with a first shell water as the donor (HD) is strengthened, while those with a first shell water as the acceptor (HA) are weakened. For a hydrated anion, this binary effect reverses, but is less significant. This ion-specific binary effect correlates with the size and the valence of the ion, and is more significant for the strong kosmotropic ions of high charge density.Water-ethanol suspensions of 2D coordination network (CN) based on rare earth elements and mixed ligands were evaluated as reactive oxygen species (ROS) generators under UV light irradiation, in contact with a biomimetic substrate (tryptophan) or an O2(1Δg) quencher (1,3-diphenylisobenzofuran; 1,3-DPBF). A combination of bottom-up and top-down strategies was implemented in order to obtain nano-sized CN particles and the subsequent colloidal suspensions were also tested towards photodynamic inactivation of Candida albicans (C. albicans). SEM, TEM, FTIR, and XRD techniques were applied to characterize the solids and ICP-AES was employed to determine the metal content of the colloidal suspensions.  https://www.selleckchem.com/products/ins018-055-ism001-055.html  Promising results were found indicating that the presence of Tb3+ allows an intersystem crossing suitable for singlet oxygen generation, resulting in the antifungal activity of C. albicans culture upon UV-irradiation.Ambient and indoor air pollution results in an estimated 7 million premature deaths globally each year, representing a major contemporary public health challenge, but one poorly quantified from a toxicological and source perspective. Indoor exposure represents possibly the greatest potential overall exposure, yet our indoor environments are still poorly understood, modelled and characterized. In rapidly growing cities, such as Lagos, Nigeria, environmental monitoring can play an important role in establishing baseline data, monitoring urban pollution trends and in environmental education. Classroom dust samples were collected from 40 locations from across the twenty local government areas (LGAs) of Lagos, in June 2019. The aim of the study was to assess the potential hazard posed by PTE in indoor dusts and to develop a suitable risk communication strategy to inform and educate the public, promoting environmental health literacy. Concentrations of total PTE in indoor dusts were assessed using Energy Dispersiveoncentrations would overestimate the hazard potential of PTE in these indoor dusts. Zinc was the most bioaccessible PTE (mean of 88%), with Mn (57%), Pb (48%), Ba (48%), Al (41%), As (37%), Cu (36%), Ni (28%), Cr (10%) and Fe (7%) the least bioaccessible. Human health risk assessment, for both children and adults using the bioaccessible fraction, showed values to be within acceptable risk levels.The mechanism of thermal decomposition and fire suppression, and the fire-extinguishing performance of HFO-1234yf, HCFO-1233xf and 2-BTP agents were investigated by using both experimental and theoretical methods. The different halogen atoms connected with the middle carbon atom result in the varied strength of C-X (X = F, Cl, Br) bonds, and thus different thermal stability of these agents, which could further affect the pyrolysis mechanism/products and the fire-extinguishing mechanism/performance of these agents. Owing to the generation of CF3˙, Cl˙ and Br˙ radicals, as well as some unsaturated small molecules produced by their pyrolysis, the HFO-1234yf, HCFO-1233xf and 2-BTP agents have minimum extinguishing concentrations (MECs) of 9.80 vol%, 7.28 vol% and 2.92 vol% (9.80 vol%, 7.28 vol% and 2.56 vol%) for suppressing propane-air (methane-air) flame, respectively, which are comparable to or even better than those of other hydrofluoroolefin (HFO) and hydrofluorocarbon (HFC) agents. Despite the contribution of directly produced Br˙ radicals, which have the lowest energy barrier and the highest efficiency in capturing free radicals, the Br˙ and CF3˙ radicals produced by the follow-up reactions with OH˙/H˙ radicals may also contribute a lot to the best fire-suppressing performance of 2-BTP. Due to the high reactivity of these unsaturated halogenated olefins and their pyrolysis products, exothermic reactions could occur between the original agents (or their pyrolysis products) and the OH˙/O radicals, thus leading to the combustion-promotion effect of the HFO-1234yf, HCFO-1233xf and 2-BTP agents. The slightest combustion-promotion effect of the 2-BTP extinguishant may result from the easier generation and best performance of the Br˙ radicals, as well as the lowest energies released by the exothermic reactions.