Mechanical and transport properties of drawn crosslinked low-density polyethylene

The values of drawing dependence of the density ρ, axial elastic modulus E, and maximum draw ratio λ of crosslinked low-density polyethylene (CLPE) rather similar to those obtained with un-crosslinked branched material of similarly low density. Very much the same applies to the equilibrium concentration of sorbed methylene chloride in the amorphous component and the zero-concentration diffusion coefficient D₀. The exponential concentration coefficient γD , however, even at the maximum draw ratio, shows no indication of the rapid increase so characteristic of the completed transformation from the lamellar to the fibrous structure. On the basis of this finding, one can understand the small deviations in the dependence of the mechanical properties between the crosslinked and uncrosslinked branched material. The segments between the crosslinks, much shorter than the free molecules, favor the formation of the interfibrillar tie molecules that limit the drawability of the sample. But since they cannot be extended to the same length as the free molecules, they contribute less to the total fraction of tie molecules per amorphous layer and hence yield a smaller axial elastic modulus.     

Interaction of NO with nanosized Ru-, Pd-, and Pt-Doped SnO2: electron paramagnetic resonance, Mössbauer, and electrical investigation

The mechanism of NO interaction with nanosized Ru(Pd,Pt)-doped SnO(2) was studied by electron paramagnetic resonance, M?ssbauer, and electric resistance measurements. Three steps were proposed for the reaction between the semiconductor oxide and the gaseous component: (i) the formation of bielectronic oxygen vacancies (V(o)) in SnO(2); (ii) their single-ionization (V(o)(*)) with injection of electrons into the SnO(2) conduction band; (iii) the subsequent transfer of electrons from V(o)(*) to [Ru(Pd,Pt)](4+). The last process induces the formation of further oxygen vacancies which reduce the transition metal centers to lower oxidation states; the redox processes is enhanced and the electrical resistance in transition metal-doped SnO(2) is stronger modified with respect to the undoped material.     

Muon spin relaxation studies of magnetic-field-induced effects in high-Tc superconductors

Muon spin relaxation measurements in high transverse magnetic fields [FORMULA: SEE TEXT] revealed strong field-induced quasistatic magnetism in the underdoped and Eu-doped (La,Sr)2CuO4 and La1.875Ba0.125CuO4, existing well above Tc and TN. The susceptibility counterpart of Cu spin polarization, derived from the muon spin relaxation rate, exhibits a divergent behavior towards T approximately 25 K. No field-induced magnetism was detected in overdoped La1.81Sr0.19CuO4, optimally doped Bi2212, and Zn-doped YBa2Cu3O7.     

Visible and near-infrared excited-state dynamics of single-walled carbon nanotubes

Excited-state lifetimes of isolated single-walled semiconducting carbon nanotubes (SWNTs) have been measured for the first time; these excited states, observed over the 400- to 1800-nm spectral domain, possess lifetimes that range from several ps to more than 100 ps. Sub-ps to ps decay components are assigned to relaxation in SWNT bundles. Interrogation of the samples with different SWNT mean diameters further confirms the dependence of the excited-state lifetime on roll-up vector. The ratio of fast and slow decaying component contributions in the first van Hove band can be viewed as a measure of the bundle content. PACS 78.67.Ch; 78.47.+p; 61.46.+w; 73.22.-f     

Dynamics of femtosecond laser interactions with dielectrics

Femtosecond laser pulses appear as an emerging and promising tool for processing wide bandgap dielectric materials for a variety of applications. This article aims to provide an overview of recent progress in understanding the fundamental physics of femtosecond laser interactions with dielectrics that may have the potential for innovative materials applications. The focus of the overview is the dynamics of femtosecond laser-excited carriers and the propagation of femtosecond laser pulses inside dielectric materials. PACS 61.80.Ba; 52.38.Mf; 42.65.Jx; 78.47.+p; 71.35.-y     

Coherent coupling of a single <Superscript>40</Superscript>Ca<Superscript>+</Superscript> ion to a high-finesse optical cavity

We demonstrate coherent coupling of the quadrupole S_1/2D_5/2 optical transition of a single trapped ⁴⁰Ca⁺ ion to the standing wave field of a high-finesse cavity. The dependence of the coupling on temporal dynamics and spatial variations of the intracavity field is investigated in detail. By precisely controlling the position of the ion in the cavity standing wave field and by selectively exciting vibrational state-changing transitions the ion’s quantized vibration in the trap is deterministically coupled to the cavity mode. We confirm coherent interaction of ion and cavity field by exciting Rabi oscillations with short resonant laser pulses injected into the cavity, which is frequency-stabilized to the atomic transition. Received: 23 August 2002 / Published online: 8 January 2003 RID="*" ID="*"Corresponding author. E-mail: christoph.becher@uibk.ac.at RID="**" ID="**"Present address: Time and Frequency Division, National Institute of Standards and Technology, Boulder, CO 80305, USA     

Groups whose non-subnormal subgroups have a transitive normality relation

This article investigates the structure of groups in which every subgroup either is subnormal or has a transitive normality relation, with special attention to the case in which subnormal subgroups have bounded defect.     

Energetic and topological analysis of the reaction of Mo and Mo2 with NH3, C2H2, and C2H4 molecules

The Density functional theory has been applied to characterize the structural features of Mo(1,2)-NH(3),-C(2)H(4), and -C(2)H(2) compounds. Coordination modes, geometrical structures, and binding energies have been calculated for several spin multiplets. It has been shown that in contrast to the conserved spin cases (Mo(1,2)-NH(3)), the interaction between Mo (or Mo(2)) and C(2)H(4) (or C(2)H(2)) are the low-spin (Mo-C(2)H(4) and -C(2)H(2)) and high-spin (Mo(2)-C(2)H(4) and -C(2)H(2)) complexes. In the ground state of Mo(1,2)-C(2)H(4) and -C(2)H(2), the metal-center always reacts with the C-C center. The spontaneous formation of the global minima is found to be possible due to the crossing between the potential energy surfaces (ground and excited states with respect to the metallic center). The bonding characterization has been performed using the topological analysis of the Electron Localization Function. It has been shown that the most stable electronic structure for a pi-acceptor ligand correlates with a maximum charge transfer from the metal center to the C-C bond of the unsaturated hydrocarbons, resulting in the formation of two new basins located on the carbon atoms (away from hydrogen atoms) and the reduction of the number of attractors of the C-C basin. The interaction between Mo(1,2) and C(2)H(4) (or C(2)H(2)) should be considered as a chemical reaction, which causes the multiplicity change. Contrarily, there is no charge transfer between Mo(1,2) and NH(3), and the partners are bound by an electrostatic interaction.     

Synthesis and characterization of new difunctional alkynylated (η-arene)(η-cycloocta-1,5-diene)ruthenium(0) complexes as molecular models for organometallic polymers

The new dialkynylated complexes Ru(η⁶-DEB-Si)(η⁴-COD), 4a, Ru(η⁶-DEBP-Si)(η⁴-COD), 4b1, Ru₂(η⁶,η⁶-DEBP)(η⁴-COD)₂, 4b2 [COD = 1,5-cyclooctadiene; DEB-Si = 1,4-bis(trimethylsilylethynyl)benzene; DEBP-Si = 4,4′-bis(trimethylsilylethynyl)biphenyl] have been synthesized by the arene exchange reaction with the complex Ru(η⁶-naphthalene)(η⁴-COD). The complexes Ru(η⁶-DEB)(η⁴-COD), 5a, and Ru(η⁶-DEBP)(η⁴-COD), 5b1, have been prepared by desilylation of the corresponding compounds 4a and 4b1. All the complexes have been fully characterized by means of spectroscopic techniques.     

1,3-Cycloaddition of nitrones in ionic liquids catalyzed by Er(III): an easy access to isoxazolidines

1,3-Dipolar cycloadditions of nitrones with alkenes afforded the corresponding isoxazolidines in ionic liquids in the presence of Er(OTf)₃. The ionic liquid and the catalyst are recycled up to five times without any specific treatment or loss of activity. Extension of the procedure to the synthesis of isoxazolidinyl nucleosides has been investigated.