Search

Background. Children are dependent on their caregivers to accurately administer medication to them.Objectives. To determine the knowledge and practices of primary caregivers regarding their methods of oral liquid medication administration, preferred measuring utensils, accuracy of preferred measuring utensils and different medication classifications that they collected. The study was conducted at Pelonomi Polyclinic Pharmacy, Bloemfontein, South Africa.Methods. A quantitative, cross-sectional descriptive study (with analytical aspects) was conducted, which used consecutive, convenient sampling. The pharmacy staff assisted in recruiting participants, after which a screening form was used to determine their eligibility. Participants were provided with an information document and consent form. The liquid medication was classified according to a drug classification list, and one medication was selected for the focus of the structured interview. The questionnaire was completed using REDCap. Thereafter, researchers used the information on the medication label to determine the accuracy of the caregiver’s answers.Results. The majority of the 89 participants (56.2%) answered all 3 administration-related questions correctly, with 84.3% answering the questions regarding quantity and frequency correctly. The medication measure (43.8%) was the preferred measuring utensil for any liquid medication at home, and the syringe (53.9%) for the selected liquid medication used in the interview, both accurate measuring utensils. Most children (56.2%) were prescribed ‘other medication’ (e.g. vitamins and mineral supplements), followed by analgesics (47.2%) and antibiotics (42.7%).Conclusion. Primary caregivers at Pelonomi Polyclinic Pharmacy know how to administer oral liquid medication to children accurately. Most caregivers indicated that they use accurate measuring utensils

We would like to thank the China Scholarships Council for a studentship to CH. PSH and WZ thank the Welch Foundation (Grant E-1457) and the National Science Foundation (DMR-2002319) for support. Two-dimensional (2D) organic−inorganichybrid copper perovskites have drawn tremendous attention as promisingmultifunctional materials. Herein, by incorporating ortho, metaand para-chlorine substitution in the benzylamine structure, we firstlyreport theinfluence of positional isomerism on the crystal structures of chlorobenzylammonium copper (II) chloride perovskites A2CuCl4. 2Dpolar ferromagnets (3-ClbaH)2CuCl4 and (4-ClbaH)2CuCl4(ClbaH+ = chlorobenzylammonium) are successfully obtained. They bothadopt a polar monoclinic space group Cc at room temperature, displayingsignificant differences in crystal structures. In contrast, (2-ClbaH)2CuCl4adopts a centrosymmetric space group P21/c at roomtemperature. This associated structural evolution successfullyenhances the physical properties of the two polar compounds with high thermalstability, discernible second harmonic generation (SHG) signals, ferromagnetism,and narrowoptical band gaps.These findings demonstrate that theintroduction of chlorine atoms into the inter-layer organicspecies is a powerful tool to tune crystalsymmetries and physical properties, and this inspires further exploration of designinghigh-performance multifunctional copper-based materials. Publisher PDF

H.L. would like to thank the University of St. Andrews for financial support via a St. Leonard’s scholarship. The authors acknowledge facilities access made possible through support from the EPSRC Light Element Analysis facility Grant EP/T019298/1 and the EPSRC Strategic Equipment Resource Grant EP/R023751/1. Vacancy-ordered halide perovskites have received great interest in optoelectronic applications. In this work, we report the novel inorganic halide Cs10MnSb6Cl30 with a distinctive 10H (10-layer hexagonal) perovskite polytype structure with (hcccc)2 stacking. Cs10MnSb6Cl30 has 30% B-site vacancies ordered at both corner- and face-sharing sites, resulting in [MnSb6Cl30]10–n columns, i.e., a reduction of octahedral connectivity to 1D. This results in enhanced photoluminescence in comparison to the previously reported 25% vacancy-ordered 3C polytype Cs4MnSb2Cl12 with 2D connectivity. This demonstrates not only the existence of the 10H perovskite structure in halides but also demonstrates the degree of B-site deficiency and stacking sequence variation as a direction to tune the optical properties of perovskite polytypes via vacancy rearrangements. Publisher PDF

JAM would like to acknowledge the School of Chemistry, University of St Andrews for the allocation of a PhD studentship through the EPSRC doctoral training grant (EP/K503162/1). AR would like to acknowledge support through the Strategic Grant POSDRU/159/1.5/S/133255, Project ID 133255 (2014), co-financed by the European Social Fund within the Sectorial Operational Program Human Resources Development 2007–2013 and also the University of Craiova and University of Cambridge for the mobility grant “Resonant ultrasound spectroscopy. (RUS) characterization of dielectric and ferroelectric tetragonal tungsten bronzes”. The work carried out at the University of St Andrews and University of Cambridge is part of an EPSRC- funded collaboration (EP/P02453X/1 and EP/P024904/1). The ‘empty’ tetragonal tungsten bronze Ba4La0.67 1.33Nb10O30 displays both relaxor-like and normal dielectric anomalies as a function of temperature; the former is associated with loss of ferroelectricity and was proposed to originate from anion disordering [Chem. Mater., 2016, 28 , 4616-4627]. Here we present total neutron scattering and pair distribution function (PDF) analysis which shows an increase in the distribution of oxygen-oxygen distances at the relaxor transition and which supports the proposed anion disordering mechanism. The disordering process can be destabilised by reducing the average A-cation size (i.e. Nd-doping: Ba4(La1-xNdx)0.67Nb10O30); this introduces a more strongly propagating tilt system in line with the previously reported crystal-chemical framework model [Chem. Mater., 2015, 27 , 3250-3261]. Mechanical loss data obtained using resonant ultrasound spectroscopy also indicate destabilisation of the disordering process with increasing Nd-substitution. Postprint

The Zoophycos group of trace fossils is common in Carboniferous to recent marine strata and sediments, and is a common component of ichnofaunas in the Visean and Namurian stages of England and Wales. A review of new and published records indicates that it is often present in limestones and sandstones of Chadian to Arnsbergian age. Thereafter it is less common, and restricted to clastic rocks. There are no known records within Carboniferous strata above the lowest Westphalian. The form is most common and often abundant in limestones of the Yoredale facies in the upper Visean and lower Namurian stages of northern England, particularly so in northern Northumberland. Where detailed sedimentological data exist, they indicate that the organisms responsible for the Zoophycos group burrowed into unconsolidated carbonate substrate that was deposited under low accumulation rates, often affected by storm wave action and where seawater flow provided a nutrient supply. However, in mixed carbonate–clastic settings, the deep-tier nature of Zoophycos may indicate that the organism lived in overlying shallow-marine, clastic-dominated depositional environments and burrowed down into the carbonate substrate. The same may be true of siliciclastic depositional settings where the presence of Zoophycos in some sandstones may reflect the palaeoenvironment of the overlying, finer-grained transgressive marine (prodelta and distal mouth bar) deposits. Supplementary material: A spreadsheet with details of Carboniferous records of Zoophycos group fossils from England, Wales, the Isle of Man and the North Sea is available at https://doi.org/10.6084/m9.figshare.c.4994636

We acknowledge the University of St Andrews and the China Scholarship Council (studentship to CH) and the University of St Andrews (studentship to AJB). We present the influence of positional isomerism on the crystal structure of fluorobenzylammonium copper (II) chloride perovskites A2CuCl4, by incorporating ortho, meta and para- fluorine substitution in the benzylamine structure. Two-dimensional (2D) polar ferromagnet (3-FbaH)2CuCl4 (3-FbaH+ = 3-fluorobenzylammonium) is successfully obtained, which crystallizes in a polar orthorhombic space group Pca21 at room temperature. In contrast, both (2-FbaH)2CuCl4 (2-FbaH+ = 2-fluorobenzylammonium) and (4-FbaH)2CuCl4 (4-FbaH+ = 4-fluorobenzylammonium) crystallize in centrosymmetric space groups P21/c and Pnma at room temperature, respectively, displaying significant differences in crystal structures. These differences indicate that the position of the fluorine atom is a driver for the polar behaviour in (3-FbaH)2CuCl4. Preliminary magnetic measurements confirm that these three perovskites possess dominant ferromagnetic interactions within the inorganic [CuCl4]∞ layers. Therefore, (3-FbaH)2CuCl4 is a polar ferromagnet, with potential as a type I multiferroic. This work is expected to promote further development of high performance 2D copper (II) halide perovskite multiferroic materials. Publisher PDF

A family of Ruddlesden–Popper (n = 1) layered perovskite-related phases, Az2PbClxBr4−x with composition 0 ≤ x ≤ 4 were obtained using mechanosynthesis. These compounds are isostructural with K2NiF4 and therefore adopt the idealised n = 1 Ruddlesden–Popper structure. A linear variation in unit cell volume as a function of anion average radius is observed. A tunable bandgap is achieved, ranging from 2.81 to 3.43 eV, and the bandgap varies in a second-order polynomial relationship with the halide composition.

Authors thank the Chinese Scholarship Council and the University of St Andrews for Ph.D. Studentship support (to JT, CSC No. 201603780020). The formation and study of partial solid solutions in Az1-xFAxPbBr3, using reportedly similar sized cations azetidinium (Az+) and formamidinium (FA+), was explored via mechanosynthesis and precipitation synthesis. The composition and lattice parameters of samples from both syntheses were analyzed by 1H NMR and Rietveld refinement of powder X-ray diffraction. A clear mismatch in the composition of the perovskite was found between the precipitated samples and the corresponding solutions. Such a mismatch was not observed for samples obtained via mechanosynthesis. The discrepancy suggests products are kinetically-controlled during precipitation, compared to thermodynamically controlled mechanosynthesis. Furthermore, the cell volume as a function of composition in both hexagonal, 6H (Az-rich) and cubic, 3C (FA-rich) perovskite solid solutions suggests that FA+ is actually smaller than Az+, contradicting the literature. In the 3C (Az-poor) solid solutions, the extent of Az1-xFAxPbBr3 is unexpectedly smaller than in the corresponding methylammonium (MA+) system, Az1-xMAxPbBr3, which suggests that the extent of solid solution formation in these halide perovskites is predominantly dependent on the average A-cation size while the size mismatch plays a lesser role in comparison to oxides. Postprint

Mixed halide azetidinium lead perovskites AzPbBr3-xXx (X = Cl or I) were obtained by mechanosynthesis. With varying halide composition from Cl- to Br- to I-; the chloride and bromide analogs both form in the hexagonal 6H polytype while the iodide adopts the 9R polytype. An intermediate 4H polytype is observed for mixed Br/I compositions. Overall the structure progresses from 6H to 4H to 9R perovskite polytype with varying halide composition. Rietveld refinement of the powder X-ray diffraction patterns revealed a linear variation in unit cell volume as a function of the average radius of the anion, which is not only observed within the solid solution of each polytype (according to Vegard’s law) but extends uniformly across all three polytypes. This is correlated with a progressive (linear) tuning of the bandgap from 3.41 to 2.00 eV. Regardless of halide, the family of azetidinium halide perovskite polytypes are highly stable, with no discernible change in properties over more than 6 months under ambient conditions