Molecular imprinting of bisphenol A and alkylphenols using amylose as a host matrix

A novel molecularly imprinted polymer has been created by a radical polymerisation of acryloylamylose in the presence of a template.     

Direct evidence for an intrinsic square vortex lattice in the overdoped high- T(c) superconductor La(1.83)Sr(0.17)CuO(4+delta)

We report here the first direct observations of a well ordered vortex lattice in the bulk of a La(2-x)Sr(x)CuO(4+delta) single crystal (slightly overdoped, x = 0.17). Our small angle neutron scattering investigation of the mixed phase reveals a crossover from triangular to square coordination with increasing magnetic field. The existence of an intrinsic square vortex lattice has never been observed in high-temperature superconductors and is indicative of the coupling of the vortex lattice to a source of anisotropy, such as those provided by a d-wave order parameter or the presence of stripes.     

Reinvestigation of the thermoelectric properties of Ag8GeTe6

High‐density polycrystalline samples (above 98% of the theoretical density) of Ag₈GeTe₆ were prepared by solid‐state reactions of Ag₂Te, GeTe, and Te, followed by hot‐pressing. The thermoelectric properties were measured at temperatures ranging from room temperature to around 700 K. The thermal conductivity values were extremely low (0.25 Wm^–1 K^–1 at room temperature), and consequently Ag₈GeTe₆ exhibited a relatively high thermoelectric figure of merit, ZT = 0.48 at 703 K. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

The synthesis of bicyclo[6.2.0]decapentaene

The parent bicyclo[6.2.0]decapentaene is synthesized for the first time by thermal ring opening of its valence isomer. Thermal dimerization of the compound is also described.     

Interpretation of electronic spectra by configuration analysis: Absorption spectra of monosubstituted naphthalenes

The electronic absorption spectra of four monosubstituted naphthalenes, α-, β-naphthols, and α-, β-naphthylamines have been investigated by means of configuration analysis with particular attention to the dependence of spectra on the position of substitution and on the electron-donating power of the substituent. The results of molecular orbital calculations based on the Pariser-Parr-Pople method are analyzed in terms of locally excited states and intramolecular charge-transfer configurations. The characteristic changes in location and polarization of the L_b, L_a, and B_b bands caused by substitution at the α- or β-position are adequately explained by the analysis. Two strong absorption bands of α-substituted naphthalenes, which appear in place of the B_b band of naphthalene, are shown to result from a mixing of the $\text{B}{}_{\mathrm{3u}}{}^{\mathrm{+}}\text{(B}{}_{\mathrm{b}}\text{)}$ and $\text{A}{}_{\mathrm{g}}{}^{\mathrm{?}}$ states. The amino group exerts a great influence on the electronic structure of the parent molecule, so that the B_b band cannot be identified in the spectrum of β-naphthylamine.     

Lasing conditions in recombining helium plasmas

Lasing conditions for He have been evaluated numerically. We have used a collisional radiative model to calculate overpopulation densities Δn_ij, which are defined as differences between population densities per unit statistical weight of the upper and lower excited levels i and j, respectively. Laser oscillations for the level pairs 2¹P-3¹S, 2¹P-4¹S, 2¹P-3¹D, 2¹P-4¹D, 3¹D-4¹F, 3¹P-4¹S, 3¹P-4¹D, and 3³P-4³S are possible when the electron densities are within well defined limits at low electron temperature (T_e = 0.1 eV). For level pairs of the singlet state, the inversion mechanism for He is the same as for H. Only collisional processes produce population inversion in the triplet level pair 3³P-4³S.