The Electronic Absorption Spectra of Binuclear Complexes,[Cu(o-phen) (sal)No3 and [Cu2 (sacch)4(im)4] Crystal

The electronic absorption spectra of crystals of the title componds were recorded and the experimental results were explained quantitatively with the ligand field theory and the radial wave function of bound Cu(II) cation. With these spactra, the range of magnetic interactions between two Cu(II) ions of the title compounds are discussed.     

Spectra Studies of Complexes Between Palladium (II), Nickel (II) and Amino Acids

The complexes of Ni (His) 2·H2O, Ni (Gly) 2·2H2O, Pd (His)Cl2·H2O and Pd(Gly) 2·2H2O were synthesized. And the IR, electronic absorption and photoacoustic spectra of these complexes were measured in solid state. The nature of the metal-carboxylate coordinate bond were deduced from the variation in the carboxyl stretching frequencies. And the d-d transition absorptions of these complexes were interpreted quantitatively with the 3d scaling radial theory. Therefore, the structural characterizations were also discussed with their spectral behaviors.     

On a new FeOF polymorph: Synthesis and stability

A new polymorph of FeOF (up to now only known in its rutile type structure) was prepared by using a new synthesis approach formally based on anionic exchange using the well-known layered FeOCl as precursor. The synthesis was achieved using [CH₃C(CH₂O–)₂(COO–)B] to vehicle fluorine through the formation of soluble (CH₃)₄N⁺ [CH₃C(CH₂O–)₂(COO–)BF]⁻ and using N,N-dimethylformamide (DMF) as the reacting medium. The XRD pattern of layered FeOF can be indexed with an orthorhombic cell which doubles along the b axis (which is the direction perpendicular to the layers) with respect to that of pristine FeOCl (a = 3.792(1) Å, b = 12.699(1) Å, c = 3.321(1) Å). Both thermal analysis and diffraction indicate similar stability for the layered and rutile polymorphs. Such findings are rationalized through Density Functional Theory calculations. It is found that the energy difference between the more stable rutile and layered polymorphs is practically nul. The origin of the similar stability lies in the fact that although the number of Fe–F and Fe–O bonds is different in the two structures, the strength of both the total number of Fe–O as well as Fe–F bonds are found to be almost identical. Even if the crystal and electronic structures are considerably different, the total bonding and thus, the stability of the two polymorphs, is comparable. The stability of different FeOF rutile type structures is also analyzed.     

Polymorphism in Bi2(SO4)3

A new polymorph of Bi₂(SO₄)₃ was prepared by reaction of LiBiO₂ with H₂SO₄ and its crystal structure was solved from X-ray powder diffraction. This new polymorph crystallizes in C2/c space group with lattice parameters a = 17.3383(3) Å, b = 6.77803(12) Å, c = 8.30978(13) Å, β = 101.4300(12)°. Bi₂(SO₄)₃ presents a layered structure made of SO₄ sulfate groups and signs of stereochemically active Bi³⁺ lone pairs. The new Bi₂(SO₄)₃ absorbs water to form Bi₂(H₂O)₂(SO₄)₂(OH)₂ through an intermediate Bi₂O(OH)₂SO₄ phase, and the transition is reversible when heated under vacuum.     

Measurement of the top quark pair production cross section in pp collisions at s=7TeV in dilepton final states with ATLAS

A measurement of the production cross section of top quark pairs ($t\overline{t}$) in proton–proton collisions at a center-of-mass energy of 7 TeV recorded with the ATLAS detector at the Large Hadron Collider is reported. Candidate events are selected in the dilepton topology with large missing transverse energy and at least two jets. Using a data sample corresponding to an integrated luminosity of $35{\mathrm{pb}}^{?1}$, a $t\overline{t}$ production cross section ${\sigma }_{t\overline{t}}=177\pm 20(\text{stat.})\pm 14(\text{syst.})\pm 7(\text{lum.})\text{pb}$ is measured for an assumed top quark mass of $m_t=172.5\text{GeV}$. A second measurement requiring at least one jet identified as coming from a b quark yields a comparable result, demonstrating that the dilepton final states are consistent with being accompanied by b-quark jets. These measurements are in good agreement with Standard Model predictions.     

Asymptotic solution for EI Nino-southern oscillation of nonlinear model

A class of nonlinear coupled system for El Nino-Southern Oscillation(ENSO) model is considered.Using the asymptotic theory and method of variational iteration,the asymptotic expansion of the solution for ENSO models is obtained.     

Investigation of thermal degradation characteristics of polyamide-6 containing melamine or melamine cyanurate via direct pyrolysis mass spectrometry

In this work the changes in thermal degradation characteristics of polyamide 6 (PA6) in the presence of melamine (Me) or melamine cyanurate (MC) were investigated systematically via direct pyrolysis mass spectrometry. Though thermal stability of PA6 was not affected by the presence of flame retardants, the changes in the products and in their distributions were detected. The reaction of carbonyl groups of PA6 with amine groups of melamine was the main cause for the changes in the product distribution. In the presence of melamine cyanurate, new products due to the reaction of cyanic acid generated by the decomposition of cyanurate, with the amine groups of PA6 were detected. Significant increases in the evolution temperatures of melamine and melamine cyanurate in the presence of PA6 were attributed to intermolecular interactions, most probably by H-bonding, with PA6.