472 research outputs found

    Spin correlations in Ca3Co2O6: A polarised-neutron diffraction and Monte Carlo study

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    We present polarised-neutron diffraction measurements of the Ising-like spin-chain compound Ca3Co2O6 above and below the magnetic ordering temperature TN. Below TN, a clear evolution from a single-phase spin-density wave (SDW) structure to a mixture of SDW and commensurate antiferromagnet (CAFM) structures is observed on cooling. For a rapidly-cooled sample, the majority phase at low temperature is the SDW, while if the cooling is performed sufficiently slowly, then the SDW and the CAFM structure coexist between 1.5 and 10 K. Above TN, we use Monte Carlo methods to analyse the magnetic diffuse scattering data. We show that both intra- and inter-chain correlations persist above TN, but are essentially decoupled. Intra-chain correlations resemble the ferromagnetic Ising model, while inter-chain correlations resemble the frustrated triangular-lattice antiferromagnet. Using previously-published bulk property measurements and our neutron diffraction data, we obtain values of the ferromagnetic and antiferromagnetic exchange interactions and the single-ion anisotropy.Comment: 10 pages, 7 figure

    Enhanced elastic stability of a topologically disordered crystalline metalā€“organic framework

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    By virtue of their open network structures and low densities, metalā€“organic frameworks (MOFs) are soft materials that exhibit elastic instabilities at low applied stresses. The conventional strategy for improving elastic stability is to increase the connectivity of the underlying MOF network, which necessarily increases material density and reduces porosity. Here we demonstrate an alternative paradigm, whereby elastic stability is enhanced in a MOF with an aperiodic network topology. We use a combination of variable-pressure single-crystal X-ray diffraction measurements and coarse-grained lattice-dynamical calculations to interrogate the high-pressure behaviour of the topologically aperiodic system TRUMOF-1,Ā which we compare against that of its ordered congener MOF-5. We show that the topology of the former quenches the elastic instability responsible for pressure-induced framework collapse in the latter, much as irregularity in the shapes and sizes of stones acts to prevent cooperative mechanical failure in drystone walls. Our results establish aperiodicity as a counterintuitive design motif in engineering the mechanical properties of framework structures, relevant to MOFs and larger-scale architectures alike

    Dental fluorosis in populations from Chiang Mai, Thailand with different fluoride exposures - Paper 2: The ability of fluorescence imaging to detect differences in fluorosis prevalence and severity for different fluoride intakes from water

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    BACKGROUND: To assess the ability of fluorescence imaging to detect a dose response relationship between fluorosis severity and different levels of fluoride in water supplies compared to remote photographic scoring in selected populations participating in an observational, epidemiological survey in Chiang Mai, Thailand. METHODS: Subjects were male and female lifetime residents aged 8-13ā€‰years. For each child the fluoride content of cooking water samples (CWS) was assessed to create categorical intervals of water fluoride concentration. Fluorescence images were taken of the maxillary central incisors and analyzed for dental fluorosis using two different software techniques. Output metrics for the fluorescence imaging techniques were compared to TF scores from blinded photographic scores obtained from the survey. RESULTS: Data from 553 subjects were available. Both software analysis techniques demonstrated significant correlations with the photographic scores. The metrics for area effected by fluorosis and the overall fluorescence loss had the strongest association with the photographic TF score (Spearmanā€™s rho 0.664 and 0.652 respectively). Both software techniques performed well for comparison of repeat fluorescence images with ICC values of 0.95 and 0.85 respectively. CONCLUSIONS: This study supports the potential use of fluorescence imaging for the objective quantification of dental fluorosis. Fluorescence imaging was able to discriminate between populations with different fluoride exposures on a comparable level to remote photographic scoring with acceptable levels of repeatability

    One-dimensional magnetic order in the metalā€“organic framework Tb(HCOO)3Tb(HCOO)_3

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    Variable-temperature neutron scattering measurements, reverse Monte Carlo analysis and direct Monte Carlo simulation are used to characterise magnetic order in the metalā€“organic framework (MOF) Tb(HCOO)3Tb(HCOO)_3 over the temperature range 100K to 1.6K = TN_N. The magnetic transition at TN_N is shown to involve one-dimensional ferromagnetic ordering to a partially-ordered state related to the triangular Ising antiferromagnet and distinct from the canonical ā€œpartially-disordered antiferromagnetā€ model. In this phase, the direction of magnetisation of ferromagnetic chains tends to alternate between neighbouring chains but this alternation is frustrated and is not itself ordered. We suggest the existence of low-dimensional magnetic order in Tb(HCOO)3Tb(HCOO)_3 is stabilised by the contrasting strength of inter- and intra-chain magnetic coupling, itself a consequence of the underlying MOF architecture. Our results demonstrate how MOFs may provide an attractive if as yet under-explored platform for the realisation and investigation of low-dimensional physics

    Carbene Complexes of Neptunium

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    Since the advent of organotransuranium chemistry six decades ago, structurally verified complexes remain restricted to Ļ€-bonded carbocycle and Ļƒ-bonded hydrocarbyl derivatives. Thus, transuranium-carbon multiple or dative bonds are yet to be reported. Here, utilizing diphosphoniomethanide precursors we report the synthesis and characterization of transuranium-carbene derivatives, namely, diphosphonio-alkylidene- and N-heterocyclic carbeneā€“neptunium(III) complexes that exhibit polarized-covalent Ļƒ2Ļ€2 multiple and dative Ļƒ2 single transuranium-carbon bond interactions, respectively. The reaction of [NpIIII3(THF)4] with [Rb(BIPMTMSH)] (BIPMTMSH = {HC(PPh2NSiMe3)2}1ā€“) affords [(BIPMTMSH)NpIII(I)2(THF)] (3Np) in situ, and subsequent treatment with the N-heterocyclic carbene {C(NMeCMe)2} (IMe4) allows isolation of [(BIPMTMSH)NpIII(I)2(IMe4)] (4Np). Separate treatment of in situ prepared 3Np with benzyl potassium in 1,2-dimethoxyethane (DME) affords [(BIPMTMS)NpIII(I)(DME)] (5Np, BIPMTMS = {C(PPh2NSiMe3)2}2ā€“). Analogously, addition of benzyl potassium and IMe4 to 4Np gives [(BIPMTMS)NpIII(I)(IMe4)2] (6Np). The synthesis of 3Npā€“6Np was facilitated by adopting a scaled-down prechoreographed approach using cerium synthetic surrogates. The thorium(III) and uranium(III) analogues of these neptunium(III) complexes are currently unavailable, meaning that the synthesis of 4Npā€“6Np provides an example of experimental grounding of 5f- vs 5f- and 5f- vs 4f-element bonding and reactivity comparisons being led by nonaqueous transuranium chemistry rather than thorium and uranium congeners. Computational analysis suggests that these NpIIIā•C bonds are more covalent than UIIIā•C, CeIIIā•C, and PmIIIā•C congeners but comparable to analogous UIVā•C bonds in terms of bond orders and total metal contributions to the Mā•C bonds. A preliminary assessment of NpIIIā•C reactivity has introduced multiple bond metathesis to transuranium chemistry, extending the range of known metallo-Wittig reactions to encompass actinide oxidation states III-VI

    Carbene Complexes of Neptunium

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    Since the advent of organotransuranium chemistry six decades ago, structurally verified complexes remain restricted to Ļ€-bonded carbocycle and Ļƒ-bonded hydrocarbyl derivatives. Thus, transuranium-carbon multiple or dative bonds are yet to be reported. Here, utilizing diphosphoniomethanide precursors we report the synthesis and characterization of transuranium-carbene derivatives, namely, diphosphonio-alkylidene- and N-heterocyclic carbeneā€“neptunium(III) complexes that exhibit polarized-covalent Ļƒ2Ļ€2 multiple and dative Ļƒ2 single transuranium-carbon bond interactions, respectively. The reaction of [NpIIII3(THF)4] with [Rb(BIPMTMSH)] (BIPMTMSH = {HC(PPh2NSiMe3)2}1ā€“) affords [(BIPMTMSH)NpIII(I)2(THF)] (3Np) in situ, and subsequent treatment with the N-heterocyclic carbene {C(NMeCMe)2} (IMe4) allows isolation of [(BIPMTMSH)NpIII(I)2(IMe4)] (4Np). Separate treatment of in situ prepared 3Np with benzyl potassium in 1,2-dimethoxyethane (DME) affords [(BIPMTMS)NpIII(I)(DME)] (5Np, BIPMTMS = {C(PPh2NSiMe3)2}2ā€“). Analogously, addition of benzyl potassium and IMe4 to 4Np gives [(BIPMTMS)NpIII(I)(IMe4)2] (6Np). The synthesis of 3Npā€“6Np was facilitated by adopting a scaled-down prechoreographed approach using cerium synthetic surrogates. The thorium(III) and uranium(III) analogues of these neptunium(III) complexes are currently unavailable, meaning that the synthesis of 4Npā€“6Np provides an example of experimental grounding of 5f- vs 5f- and 5f- vs 4f-element bonding and reactivity comparisons being led by nonaqueous transuranium chemistry rather than thorium and uranium congeners. Computational analysis suggests that these NpIIIā•C bonds are more covalent than UIIIā•C, CeIIIā•C, and PmIIIā•C congeners but comparable to analogous UIVā•C bonds in terms of bond orders and total metal contributions to the Mā•C bonds. A preliminary assessment of NpIIIā•C reactivity has introduced multiple bond metathesis to transuranium chemistry, extending the range of known metallo-Wittig reactions to encompass actinide oxidation states III-VI

    Climate, landscape, habitat, and woodland management associations with hazel dormouse Muscardinus avellanarius population status

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    Although strictly protected, populations of the hazel dormouse Muscardinus avellanarius in the UK declined by 72% from 1993 to 2014. Using National Dormouse Monitoring Programme data from 300 sites throughout England and Wales, we investigated variation in hazel dormouse population status (expressed as Indices of Abundance, Breeding, and population Trend) in relation to climate, landscape, habitat, and woodland management. Dormice were more abundant and produced more litters on sites with warmer, sunnier springs, summers, and autumns. Dormouse abundance was also higher on sites with consistently cold local climate in winter. Habitat connectivity, woodland species composition, and active site management were all correlated with greater dormouse abundance and breeding. Abundances were also higher on sites with successional habitats, whereas the abundance of early successional bramble Rubus fruticosus habitat, woodland area, and landscape connectivity were important for population stability. Diversity in the structure of woodlands in Europe has decreased over the last 100 years, and the habitats we found to be associated with more favourable dormouse status have also been in decline. The conservation status of the hazel dormouse, and that of woodland birds and butterflies, may benefit from reinstatement or increased frequency of management practices, such as coppicing and glade management, that maintain successional and diverse habitats within woodland
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