Astrometric observations of Phobos and Deimos during the 1971 opposition of Mars

Accurate positional measurements of planets and satellites are used to improve our knowledge of their dynamics and to infer the accuracy of planet and satellite ephemerides. In the framework of the FP7 ESPaCE project, we provide the positions of Mars, Phobos, and Deimos taken with the U.S. Naval Observatory 26-inch refractor during the 1971 opposition of the planet. These plates were measured with the digitizer of the Royal Observatory of Belgium and reduced through an optimal process that includes image, instrumental, and spherical corrections to provide the most accurate data. We compared the observed positions of the planet Mars and its satellites with the theoretical positions from INPOP10 and DE430 planetary ephemerides, and from NOE and MAR097 satellite ephemerides. The rms residuals in RA and Dec. of one position is less than 60 mas, or about 20 km at Mars. This accuracy is comparable to the most recent CCD observations. Moreover, it shows that astrometric data derived from photographic plates can compete with those of old spacecraft (Mariner 9, Viking 1 and 2).Comment: 5 pages, 3 figure

Investigation of octupole vibrational states in 150Nd via inelastic proton scattering (p,p'g)

Octupole vibrational states were studied in the nucleus $^{150}\mathrm{Nd}$ via inelastic proton scattering with \unit[10.9]{MeV} protons which are an excellent probe to excite natural parity states. For the first time in $^{150}\mathrm{Nd}$, both the scattered protons and the $\gamma$ rays were detected in coincidence giving the possibility to measure branching ratios in detail. Using the coincidence technique, the $B(E1)$ ratios of the decaying transitions for 10 octupole vibrational states and other negative-parity states to the yrast band were determined and compared to the Alaga rule. The positive and negative-parity states revealed by this experiment are compared with Interacting Boson Approximation (IBA) calculations performed in the (spdf) boson space. The calculations are found to be in good agreement with the experimental data, both for positive and negative-parity states

Investigations into the reactivity of lithium indenyl with alpha diimines with chlorinated backbones and formation of related functional ligands and metal complexes

Reaction between lithium indenyl and a chlorine substituted alpha diimine of the form [{Cl(NPh)2}C)]2 unexpectedly yielded the corresponding NH rearranged derivative [PhN(H)C(C9H6)]2 (1) rather than the predicted symmetrical α-diimine. This compound 1 was characterised by 1H NMR, 13C{1H} NMR and mass spectrometry, and additionally by X-ray diffraction. It was found that 1 was the first indene-substituted and symmetric secondary amine which was also highly fluorescent in DMSO. The reactivity of 1 towards simple inorganic and organometallic transition metals precursors based on the MX2 fragments, where M = Group 10 metals and X = halides or methyl groups, has been investigated. Surprisingly, the reaction with [PtMe2(COD)] led to the coupling reaction between the indenyl groups incorporated at the C-C ligand backbone and a new ligand (2) was discovered, in an attempt to synthesise the metal-linked diamine. Single crystal X-ray diffraction studies confirm this compound 2 to feature coupled indenyl residues and delocalised C-C bonds in the solid state. Structural authentication by X-ray crystallography showed compound 2 to be a very rare example of flat and extended aromatic organic molecule and mass spectrometry, IR and NMR spectroscopy were carried out to gain further insight into the solid state and solution phase structures. Further experiments to synthesise analogues of [PhN(H)C(Ind)]2 aiming to shift a likely equilibrium in favour the imine tautomer, by introducing bulky ortho substituents onto the benzene ring (R = Me, iPr) showed the presence of the imine tautomer to be increasingly favoured in 1H NMR spectra, with an increase in the steric bulk of the ortho substituents. However, the enamine tautomer is still observed to a minor extent even with isopropyl substituents and yields of these desired compounds were low on steric grounds.</p

Explorations into peptide nucleic acid contrast agents as emerging scaffolds for breakthrough solutions in medical imaging and diagnosis

Peptide nucleic acids (PNAs, nucleic acid analogues with a peptide backbone rather than a phosphoribosyl backbone) have emerged as promising chemical agents in antigene or antisense therapeutics, as splicing modulators or in gene editing. Their main benefits, compared to DNA or RNA agents, are their biochemical stability and the lack of negative charges throughout the backbone, leading to negligible electrostatic interaction with the strand with which they are hybridizing. As a result, hybridization of PNA strands with DNA or RNA strands leads to higher binding energies and melting temperatures. A lack of natural transporters, however, necessitates the formation of PNA-containing chimeras or the formulation of nanoparticular cell delivery methods. Here, we set out to explore the progress made in using imaging agents based on PNAs in diagnostic applications and highlight selected developments and challenges

Dilution in Laser Cladding with Ni-Based Powders

This study addresses to the laser cladding of nickel-based powders on stainless steel substrate. A TRUMPH pulsed laser and a coaxial cladding module are used to fabricate single tracks on AISI 304 substrate. The influence of the laser power on the geometric characteristics and microstructure of the cladded layer is investigated using optical and scanning electron microscopy and energy dispersive X-ray spectroscopy. Dilution is determined using the melt depth of the cladded tracks and validated using the local chemical microanalysis. The results showed that laser power have a major influence on the dilution and melted area of the laser cladded tracks

The role of the emergency medical dispatch centre (EMDC) and prehospital emergency care safety: results from an incident report (IR) system

Introduction The role of the emergency medical dispatch centre (EMDC) is essential to ensure coordinated and safe prehospital care. The aim of this study was to implement an incident report (IR) system in prehospital emergency care management with a view to detecting errors occurring in this setting and guiding the implementation of safety improvement initiatives

Influence of Titanium Additions on The Electrochemical Behaviour of NiCr/Ti Laser Cladded Coatings

In this research, the electrochemical evaluation of NiCr/Ti laser cladded coatings in simulated polymer electrolyte membrane fuel cells (PEMFCs) environment was investigated. The Laser Cladding technique was used to develop protective coatings on mild steel substrate using NiCr-based powders mixed with 12.5, 15, 17.5 and 20 wt.% Ti additions. The samples were tested at room temperature in Na2SO4 0.1M + 0.1 ppm F-. The potentiodynamic polarization curves are presented before and after the samples were subjected to accelerated stress tests, for 6 hours each, at +0.736 V (cathodic environment) and at -0.493 V (anodic environment). Afterwards, scanning electron microscopy (SEM) was used to investigate the effect of Ti addition in terms of morphology. Energy-dispersive X-ray spectroscopy (EDS) was performed for chemical evaluation of the surface after corrosion tests

Ruthenium polypyridyl complexes and their modes of interaction with DNA : is there a correlation between these interactions and the antitumor activity of the compounds?

Various interaction modes between a group of six ruthenium polypyridyl complexes and DNA have been studied using a number of spectroscopic techniques. Five mononuclear species were selected with formula [Ru(tpy) L1L2](2-n)?, and one closely related dinuclear cation of formula [{Ru(apy)(tpy)}2{l-H2N(CH2)6NH2}]4?. The ligand tpy is 2,20:60,200-terpyridine and the ligand L1 is a bidentate ligand, namely, apy (2,20-azobispyridine), 2-phenylazopyridine, or 2-phenylpyridinylmethylene amine. The ligand L2 is a labile monodentate ligand, being Cl-, H2O, or CH3CN. All six species containing a labile L2 were found to be able to coordinate to the DNA model base 9-ethylguanine by 1H NMR and mass spectrometry. The dinuclear cationic species, which has no positions available for coordination to a DNA base, was studied for comparison purposes. The interactions between a selection of four representative complexes and calf-thymus DNA were studied by circular and linear dichroism. To explore a possible relation between DNA-binding ability and toxicity, all compounds were screened for anticancer activity in a variety of cancer cell lines, showing in some cases an activity which is comparable to that of cisplatin. Comparison of the details of the compound structures, their DNA binding, and their toxicity allows the exploration of structure–activity relationships that might be used to guide optimization of the activity of agents of this class of compounds