Metal-Metal Bonding in Uranium-Group 10 Complexes

Heterobimetallic complexes containing short uranium–group 10 metal bonds have been prepared from monometallic IU^IV(OAr^P-κ²<i>O</i>,<i>P</i>)₃ (<b>2</b>) {[Ar^PO]⁻ = 2-<i>tert</i>-butyl-4-methyl-6-(diphenylphosphino)­phenolate}. The U–M bond in IU^IV(μ-OAr^P-1κ¹<i>O</i>,2κ¹<i>P</i>)₃M⁰, M = Ni (<b>3–Ni</b>), Pd (<b>3–Pd</b>), and Pt (<b>3–Pt</b>), has been investigated by experimental and DFT computational methods. Comparisons of <b>3–Ni</b> with two further U–Ni complexes XU^IV(μ-OAr^P-1κ¹<i>O</i>,2κ¹<i>P</i>)₃Ni⁰, X = Me₃SiO (<b>4</b>) and F (<b>5</b>), was also possible via iodide substitution. All complexes were characterized by variable-temperature NMR spectroscopy, electrochemistry, and single crystal X-ray diffraction. The U–M bonds are significantly shorter than any other crystallographically characterized d–f-block bimetallic, even though the ligand flexes to allow a variable U–M separation. Excellent agreement is found between the experimental and computed structures for <b>3–Ni</b> and <b>3–Pd</b>. Natural population analysis and natural localized molecular orbital (NLMO) compositions indicate that U employs both 5f and 6d orbitals in covalent bonding to a significant extent. Quantum theory of atoms-in-molecules analysis reveals U–M bond critical point properties typical of metallic bonding and a larger delocalization index (bond order) for the less polar U–Ni bond than U–Pd. Electrochemical studies agree with the computational analyses and the X-ray structural data for the U–X adducts <b>3–Ni</b>, <b>4</b>, and <b>5</b>. The data show a trend in uranium–metal bond strength that decreases from <b>3–Ni</b> down to <b>3–Pt</b> and suggest that exchanging the iodide for a fluoride strengthens the metal–metal bond. Despite short U–TM (transition metal) distances, four other computational approaches also suggest low U–TM bond orders, reflecting highly transition metal localized valence NLMOs. These are more so for <b>3–Pd</b> than <b>3–Ni</b>, consistent with slightly larger U–TM bond orders in the latter. Computational studies of the model systems (PH₃)₃MU­(OH)₃I (M = Ni, Pd) reveal longer and weaker unsupported U–TM bonds vs <b>3</b>

Theory-guided enhancement of CO2 reduction to ethanol on Ag-Cu tandem catalysts via particle-size effects

In the CO2 reduction reaction, the design of electrocatalysts that selectively promote alcohols over hydrocarbons (e.g., ethanol over ethylene) hinges on the understanding of the pathways and specific sites that forms alcohols. Herein, theoretical considerations guide state-of-the-art synthesis of well-defined catalysts to show that higher selectivity toward ethanol is achieved on Cu(110) edge sites compared to Cu(100) terraces. Specifically, we study the catalytic behavior of Cu nano-cubes (Cucub) of different sizes in the framework of tandem catalysis with CO-producing Ag nanospheres. We predict and experimentally find that the smaller Cucub possess higher selectivity for ethanol in view of their larger edge-to-faces ratio and of the fact that ethylene is produced at terraces while ethanol is selectively produced at step edges. These results call for synthetic developments toward Cu nanostructures exposing only edge sites, such as hollow cubic nanocages, to further increase ethanol selectivity. More generally, this study encourages the application of well-defined nano catalysts as a bridge between theory and experiments in electrocatalysis.This work was financially supported by Gaznat S.A. J.R.P. acknowledges the H2020 Marie Curie Individual Fellowship grant SURFCAT with Agreement No. 837378. This publication was created as part of NCCR Catalysis, a National Centre of Competence in Research funded by the Swiss National Science Foundation. The theoretical effort was supported by Spanish MICIUN’s RTI2018-095460–B-I00, Ramón y Cajal RYC-2015-18996, and María de Maeztu MDM-2017-0767 Grants, and partly by Generalitat de Catalunya via 2017SGR13. M.J.K. and F.C.V. are thankful to Red Española de Supercomputación (RES) for supercomputing time at SCAYLE (Projects QS-2019-3-0018, QS-2019-2-0023, and QCM-2019-1-0034). The use of supercomputing facilities at SURFsara was sponsored by NWO Physical Sciences

Polynuclear alkoxy–zinc complexes of bowl-shaped macrocycles and their use in the copolymerisation of cyclohexene oxide and CO2

The reactions between alcohols and the tetranuclear ethyl-Zn complexes of an ortho-phenylene-bridged polypyrrole macrocycle, Zn4Et4(L1) 1 and the related anthracenyl-bridged macrocyclic complex, Zn4Et4(THF)4(L2) 2 have been studied. With long-chain alcohols such as n-hexanol, the clean formation of the tetranuclear hexoxide complex Zn4(OC6H13)4(L1) 3 occurs. In contrast, the use of shorter-chain alcohols such as i-propanol results in the trinuclear complex Zn3(μ2-OiPr)2(μ3-OiPr)(HL1) 4 that arises from demetalation; this complex was characterised by X-ray crystallography. The clean formation of these polynuclear zinc clusters allowed a study of their use as catalysts in the ring-opening copolymerisation (ROCOP) reaction between cyclohexene oxide and CO2. In situ reactions involving the pre-catalyst 1 and n-hexanol formed the desired polymer with the best selectivity for polycarbonate (90%) at 30 atm CO2, whilst the activity and performance of pre-catalyst 2 was poor in comparison

Pressure-induced inclusion of neon in the crystal structure of a molecular Cu2(pacman) complex at 4.67 GPa

Crystals of a Cu complex of the macrocyclic Schiff-base calixpyrrole or 'Pacman' ligand, Cu2(L), do not contain any solvent-accessible void space at ambient pressure, but adsorb neon at 4.67 GPa, forming Cu2(L)·3.5Ne

Towards dipyrrins:oxidation and metalation of acyclic and macrocyclic Schiff-base dipyrromethanes

Oxidation of acyclic Schiff-base dipyrromethanes cleanly results in dipyrrins, whereas the macrocyclic ‘Pacman’ analogues either decompose or form new dinuclear copper(ii) complexes that are inert to ligand oxidation.</p

Earth-Abundant Mixed-Metal Catalysts for Hydrocarbon Oxygenation

The oxygenation of aliphatic and aromatic hydrocarbons using earth-abundant Fe and Cu catalysts and “green” oxidants such as hydrogen peroxide is becoming increasingly important to atom-economical chemical processing. In light of this, we describe that dinuclear Cu^II complexes of pyrrolic Schiff-base macrocycles, in combination with ferric chloride (FeCl₃), catalyze the oxygenation of π-activated benzylic substrates with hydroperoxide oxidants at room temperature and low loadings, representing a novel design in oxidation catalysis. Mass spectrometry and extended X-ray absorption fine structure analysis indicate that a cooperative action between Cu^II and Fe^III occurs, most likely because of the interaction of FeCl₃ or FeCl₄^– with the dinuclear Cu^II macrocycle. Voltammetric measurements highlight a modulation of both Cu^II and Fe^III redox potentials in this adduct, but electron paramagnetic resonance spectroscopy indicates that any Cu–Fe intermetallic interaction is weak. High ketone/alcohol product ratios, a small reaction constant (Hammett analysis), and small kinetic isotope effect for H-atom abstraction point toward a free-radical reaction. However, the lack of reactivity with cyclohexane, oxidation of 9,10-dihydroanthracene, oxygenation by the hydroperoxide MPPH (radical mechanistic probe), and oxygenation in dinitrogen-purge experiments indicate a metal-based reaction. Through detailed reaction monitoring and associated kinetic modeling, a network of oxidation pathways is proposed that includes “well-disguised” radical chemistry via the formation of metal-associated radical intermediates

Delayed consultation among pulmonary tuberculosis patients: a cross sectional study of 10 DOTS districts of Ethiopia

<p>Abstract</p> <p>Background</p> <p>Delays seeking care increase transmission of pulmonary tuberculosis and hence the burden of tuberculosis, which remains high in developing countries. This study investigates patterns of health seeking behavior and determines risk factors for delayed patient consultation at public health facilities in 10 districts of Ethiopia.</p> <p>Methods</p> <p>New pulmonary TB patients ≥ 15 years old were recruited at 18 diagnostic centres. Patients were asked about their health care seeking behaviour and the time from onset of symptoms to first consultation at a public health facility. First consultation at a public health facility 30 days or longer after onset of symptoms was regarded as prolonged patient delay.</p> <p>Results</p> <p>Interviews were held with 924 pulmonary patients. Of these, 537 (58%) were smear positive and 387 (42%) were smear negative; 413 (45%) were female; 451 (49%) were rural residents; and the median age was 34 years. Prior to their first consultation at a public health facility, patients received treatment from a variety of informal sources: the Orthodox Church, where they were treated with holy water (24%); private practitioners (13%); rural drug vendors (7%); and traditional healers (3%). The overall median patient delay was 30 days (mean = 60 days). Fifty three percent [95% Confidence Intervals (CI) (50%, 56%)] of patients had delayed their first consultation for ≥ 30 days. Patient delay for women was 54%; 95% CI (54%, 58%) and men 51%; 95% CI (47%, 55%). The delay was higher for patients who used informal treatment (median 31 days) than those who did not (15 days). Prolonged patient delay (≥ 30 days) was significantly associated with both patient-related and treatment-related factors. Significant patient-related factors were smear positive pulmonary disease [Adjusted Odds Ratio (AOR) 1.4; 95% CI (1.1 to 1.9)], rural residence [AOR 1.4; 95% CI (1.1 to 1.9)], illiteracy [AOR 1.7; 95% CI (1.2 to 2.4)], and lack of awareness/misperceptions of causes of pulmonary TB. Significant informal treatment-related factors were prior treatment with holy water [AOR 3.5; 95% CI (2.4 to 5)], treatment by private practitioners [AOR 1.7; 95% CI (1.1 to 2.6)] and treatment by drug vendors [AOR 1.9; 95% CI (1.1 to 3.5)].</p> <p>Conclusion</p> <p>Nearly half of pulmonary tuberculosis patients delayed seeking health care at a public health facility while getting treatment from informal sources. The involvement of religious institutions and private practitioners in early referral of patients with pulmonary symptoms and creating public awareness about tuberculosis could help reduce delays in starting modern treatment.</p

Abbot Ice Shelf, structure of the Amundsen Sea continental margin and the southern boundary of the Bellingshausen Plate seaward of West Antarctica

Inversion of NASA Operation IceBridge airborne gravity over the Abbot Ice Shelf in West Antarctica for subice bathymetry defines an extensional terrain made up of east-west trending rift basins formed during the early stages of Antarctica/Zealandia rifting. Extension is minor, as rifting jumped north of Thurston Island early in the rifting process. The Amundsen Sea Embayment continental shelf west of the rifted terrain is underlain by a deeper, more extensive sedimentary basin also formed during rifting between Antarctica and Zealandia. A well-defined boundary zone separates the mildly extended Abbot extensional terrain from the deeper Amundsen Embayment shelf basin. The shelf basin has an extension factor, b, of 1.5–1.7 with 80–100 km of extension occurring across an area now 250 km wide. Following this extension, rifting centered north of the present shelf edge and proceeded to continental rupture. Since then, the Amundsen Embayment continental shelf appears to have been tectonically quiescent and shaped by subsidence, sedimentation, and the advance and retreat of the West Antarctic Ice Sheet. The Bellingshausen Plate was located seaward of the Amundsen Sea margin prior to incorporation into the Antarctic Plate at about 62 Ma. During the latter part of its independent existence, Bellingshausen plate motion had a clockwise rotational component relative to Antarctica producing convergence across the north-south trending Bellingshausen Gravity Anomaly structure at 94°W and compressive deformation on the continental slope between 94°W and 102°W. Farther west, the relative motion was extensional along an east-west trending zone occupied by the Marie Byrd Seamounts

Standardisation of magnetic nanoparticles in liquid suspension

Suspensions of magnetic nanoparticles offer diverse opportunities for technology innovation, spanning a large number of industry sectors from imaging and actuation based applications in biomedicine and biotechnology, through large-scale environmental remediation uses such as water purification, to engineering-based applications such as position-controlled lubricants and soaps. Continuous advances in their manufacture have produced an ever-growing range of products, each with their own unique properties. At the same time, the characterisation of magnetic nanoparticles is often complex, and expert knowledge is needed to correctly interpret the measurement data. In many cases, the stringent requirements of the end-user technologies dictate that magnetic nanoparticle products should be clearly defined, well characterised, consistent and safe; or to put it another way—standardised. The aims of this document are to outline the concepts and terminology necessary for discussion of magnetic nanoparticles, to examine the current state-of-the-art in characterisation methods necessary for the most prominent applications of magnetic nanoparticle suspensions, to suggest a possible structure for the future development of standardisation within the field, and to identify areas and topics which deserve to be the focus of future work items. We discuss potential roadmaps for the future standardisation of this developing industry, and the likely challenges to be encountered along the way

Review of the projected impacts of climate change on coastal fishes in southern Africa

The coastal zone represents one of the most economically and ecologically important ecosystems on the planet, none more so than in southern Africa. This manuscript examines the potential impacts of climate change on the coastal fishes in southern Africa and provides some of the first information for the Southern Hemisphere, outside of Australasia. It begins by describing the coastal zone in terms of its physical characteristics, climate, fish biodiversity and fisheries. The region is divided into seven biogeographical zones based on previous descriptions and interpretations by the authors. A global review of the impacts of climate change on coastal zones is then applied to make qualitative predictions on the likely impacts of climate change on migratory, resident, estuarine-dependent and catadromous fishes in each of these biogeographical zones. In many respects the southern African region represents a microcosm of climate change variability and of coastal habitats. Based on the broad range of climate change impacts and life history styles of coastal fishes, the predicted impacts on fishes will be diverse. If anything, this review reveals our lack of fundamental knowledge in this field, in particular in southern Africa. Several research priorities, including the need for process-based fundamental research programs are highlighted