Tungsten(V) dimeric thio-complexes with dithiocarbamate ligands

The syntheses of four new tungsten(V) dimeric thio-complexes with disulphido bridge are reported. The complexes have been identified by IR and electronic spectra, magnetic susceptibilities and analytical data. On the basis of the physical measurements we propose these complexes the following formula W₂S₄(Rdtc)₂, where dtc = dithiocarbamate and R = morpholine, piperidine, N-ethylaniline and N,N-methylcyclohexyl. The low values of magnetic moments show a WW interaction. IR spectral results support a bidentate ligand behaviour and show a band in the 550-525 cm^?1 region, that we attribute to a W  S bond.     

Magnetic and structural properties of the Nd2(Fe100−x Nb x )14B system prepared by arc melting

In this work the magnetic and structural properties are investigated by Mössbauer spectrometry, Vibrating Sample Magnetometry and X-ray diffraction of Nd₂(Fe_100?x Nb _x )₁₄B powdered alloys with x?=?0, 2 and 4 prepared by arc melting. The Mössbauer spectra of the samples were fitted with several contributions from: Nd₂Fe₁₄B, α-Fe and a paramagnetic phase associated with Nd_1.1Fe₄B₄ for x?=?0 and additionally from NbFeB and Nd₂Fe₁₇ for x?=?2 and x?=?4. The relative fractions of α-Fe and Nd₂Fe₁₄B are smaller for x?=?4 than for x?=?0, indicating that the amount of these two phases is reduced with increasing Nb content, while the relative fraction of Nd₂Fe₁₇ increases. The α-Fe grain size slightly decreases while that of the Nd₂Fe₁₄B phase is increasing, when the Nb content increases. The hysteresis loops indicate that these samples behave as hard ferromagnets, with a coercive field which decreases when the Nb content increases, but with rather low remanent magnetization.     

φ meson production in NA60

NA60 is a fixed-target experiment at the CERN SPS which measured dimuon production in nucleus–nucleus and proton–nucleus collisions. The experiment collected muon pair samples of unprecedented quality in heavy-ion experiments. This paper presents a high quality measurement of the p_T distribution of the φ meson, covering a broad p_T window. The data were collected in 2003 in In-In collisions at 158 GeV per nucleon. The results, presented as a function of centrality, were studied against several possible sources of systematic effects and proved to be fairly stable. We show that the inverse m_T slope measured in In-In collisions, in the φ→μμ decay channel, depends significantly on the range used to perform the fit. When the fit is performed at low transverse momentum, the effective inverse slope increases from peripheral to central collisions, as measured by other experiments. We finally show that our measurement for In-In is compatible with the overall systematics of T slope versus mass, measured in different collision systems by the NA49 experiment PACS 25.75.Nq; 25.75.-q; 25.75.Dw; 14.40.Cs; 12.38.Mh     

Optical properties of Er doped GeO2-PbO glass: Effect of doping with Bi2O3

The optical properties of binary and ternary germanate glasses 40.3GeO₂-59.7PbO, 31.3GeO₂-26.8PbO-41.9Bi₂O₃ and 31.5GeO₂-40.4PbO-28.1Bi₂O₃ (wt%) doped with Er³⁺ were investigated. The Judd-Ofelt intensity parameters were calculated and the near-infrared luminescence as well as the upconversion efficiency was analyzed. We observed that the ternary germanate glass containing the highest concentration of Bi₂O₃ presented the largest emission bandwidth for ⁴I_13/2 → ⁴I_15/2 transition and the highest infrared-to-visible upconversion efficiency among the samples studied. These results demonstrate that not only the presence of Bi₂O₃ but also the careful choice of its molecular weight plays a key role in optimizing parameters for using germanate glasses for photonics applications.     

Improved limit on the rate of the decay K+ --> pi(+)&mgr;(+)e(-)

We report results of a search for the lepton-family number violating decay K+-->pi(+)&mgr;(+)e(-) from data collected by experiment E865 in 1996 at the Alternating Gradient Synchroton of Brookhaven National Laboratory. We place an upper limit on the branching ratio at 3.9x10(-11) ( 90% C.L.). Together with results based on data collected in 1995 and an earlier experiment, E777, this result establishes a combined 90% confidence level upper limit on the branching ratio at 2.8x10(-11). We also report a new upper limit on the branching ratio for pi(0)-->&mgr;(+)e(-) of 3.8x10(-10) ( 90% C. L.).     

Synthesis and characterization of new soluble polyamides derived from 2,6-bis(4-aminophenyl)-3,5-dimethyltetrahydro-4H-pyran-4-one

A new oxypyrone diamine, 2,6-bis(4-aminophenyl)-3,5-dimethyltetrahydro-4H-pyran-4-one (DAPP), was prepared from 4-nitrobenzaldehyde and 3-oxa-n-pentane in a two-step reaction with a high yield and a high purity. Aromatic polyamides were obtained from this novel condensation monomer and several diacid chlorides through the conventional low-temperature solution method in N,N-dimethylacetamide. Polycondensation results were consistent with a high reactivity for DAPP because high yields and high molecular weight polyamides were obtained with inherent viscosities up to 1.8 dL/g. The reactivity of DAPP was also estimated with theoretical calculations from computer programs for molecular simulation, with orbital and charge factors considered. The polymers showed improved solubility in organic solvents, relative to conventional wholly aromatic polyamides, and high glass-transition temperatures (from differential scanning calorimetry) over 270 °C. However, the thermal resistance, as estimated by thermogravimetric analysis, was lower than that of conventional aromatic polyamides; nevertheless, decomposition temperatures well beyond 300 °C were observed in nitrogen and air. © 2001 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 39: 1825–1832, 2001     

Novel Cobalt (II) Phthalocyanine‐Containing Polyimides: Synthesis,Characterization, Thermal and Optical Properties

Summary: A novel class of polymer has been prepared by reaction of a copolyimide containing carboxylic acid groups, and a cobalt phthalocyanine peripherally substituted with a reactive hydroxyl group. The incorporation of the phthalocyanine ring was achieved by esterification of the carboxylic acid groups of the polyimide with the free hydroxyl group of the phthalocyanine. In this work, a limited number of phthalocyanine rings have been introduced in order to avoid extensive modification of the copolyimide properties. The extent of modification (percentage of esterified carboxylic groups) was estimated to be about 18%. The resulting material showed good thermal stability and a high glass transition temperature (above 300 °C). The incorporation of the bulky phthalocyanine ring brought about a light decrease of thermal properties, relative to those of the initial polyimide. The presence of phthalocyanine was confirmed by the absorption band at 670 nm showing in the visible region for the modified polyimide. The novel copolyimide also exhibited a remarkable emission peak at 430 nm, when excited at 350 nm, corresponding to the emission of the cobalt phthalocyanine moiety.

Schematic representation of the PI‐CoPc molecule and the chemical structure of the repeat unit.