A supramolecular hydrogen‐bonded complex between 1,3,5‐tris(diisobutylhydroxysilyl)benzene and trans‐bis(4‐pyridyl)ethylene

The trisilanol 1,3,5‐(HOi‐Bu₂Si)₃C₆H₃ ( 7 ), prepared in three steps from 1,3,5‐tribromobenzene via the intermediates 1,3,5‐(Hi‐Bu₂Si)₃C₆H₃ ( 8 ) and 1,3,5‐(Cli‐Bu₂Si)₃C₆H₃ ( 9 ) forms an equimolar complex with trans‐bis(4‐pyridyl)ethylene (bpe), 7 ·bpe, whose structure was investigated by X‐ray crystallography. The hydrogen‐bonded network features a number of SiO? H(H)Si and SiO? H hydrogen bridges. Evidence was found for cooperative strengthening within the sequential hydrogen bonds. Copyright © 2007 John Wiley & Sons, Ltd.     

Methods and Results of Optical Investigations on Semiconductor Interfaces

Measurement of the state of polarization of reflected light (ellipsometry) permits the determination of the thickness and refractive index of thin layers formed on a surface. The IR absorption spectra of such thin layers, which can be measured by means of internal reflection spectroscopy (IRS), provide information about their chemical composition. These methods have been used to study adsorption processes and the formation of reaction layers at semiconductor interfaces, and may also be used for measurements of free charge carriers in the space-charge region and in surface states. Results of such investigations are given in this article.     

Interaction of Pd-overlayers with SnO2: comparative XPS, SIMS, and SNMS studies

Summary We report about interaction processes between palladium (Pd) and tin dioxide (SnO₂) studied with various surface spectroscopic techniques. Total sputter yields necessary for absolute depth calibration in SIMS are determined for SnO₂. Clustering of palladium occurs at low temperatures. Small changes in the XPS relative core level intensities of Pd and Sn allow to determine cluster sizes. Oxidation of Pd in the presence of oxygen at T470 K is a prerequisite for diffusion of Pd²⁺ ions into SnO₂ layers. The latter process is confirmed and described quantitatively by evaluating the SIMS and SNMS measurements.     

Elastic properties of monoclinic telluric acid ammonium phosphate,Te(OH)6·2NH4H2PO4·(NH4)2HPO4, near the paraelectric-ferroelectric transition

The elastic constants of Te(OH)₆·2NH₄H₂PO₄·(NH₄)₂HPO₄, TAAP, point symmetrym, have been measured by ultrasonic resonance methods passing through the paraelectric-ferroelectric transition at ca. 320 K. In the range between 273 and 340 K the elasticity tensor exhibits only a slight anisotropy. No discontinuity of the elastic constants is observed. However, some temperature derivatives of the elastic constants show slight anomalies within the range 310 to 325 K. The strongest effect occurs with the longitudinal elastic resistancec ₂₂. The thermal expansion which varies only slightly between 263 and 340 K, is highly anisotropic in contrast to the thermoelastic behaviour. A strong negative thermal expansion is observed in a direction within the mirror plane, ca. 45° apart from the direction of spontaneous polarization.This effect is not accompanied by a corresponding thermoelastic anomaly. The interactions connected with the transition are of the totally symmetric type. Like many other properties the elastic and thermoelastic behaviour of TAAP resembles that of triglycine sulphate (TGS). Larger differences between TAAP and TGS are found in the pressure dependence of various properties. For example the pressure dependence of the transition temperatureT is negative for TAAP (–3.8 K/kbar) and positive for TGS (3.9 K/kbar).Dedicated to Prof. Dr. H.E. Müser on the occasion of his 60th birthday     

SIMS and flash desorption studies of nickel oxygen interaction

O₂ exposure of polycrystalline nickel at 300 K results in characteristics changes of secondary ion emission. These can be described by a model which is in good agreement with corresponding LEED, AES, XPS, and ΔΦ results of other authors. According to this model, oxygen can be bonded on Ni in at least five different phases:

1. chemisorption, indicated by a rapid increase of Ni⁺, Ni ₂ ⁺ , and Ni₂O⁺ (≦5 L);
2. a rearranged chemisorption layer, characterized by a drastic decrease of Ni⁺, Ni ₂ ⁺ , and Ni₂O⁺ (5–15 L);
3. nickel oxide (NiO) responsible for a strong NiO^?- and NiO ₂ ^? -emission (≦40 L);
4. oxygen on top of this NiO layer, producing a final increase of Ni⁺ and NiO⁺ and a O₂-flash signal at 400 K (>40 L);
5. bulk dissolved oxygen in thermal equilibrium with a chemisorption layer (after several exposure/heating cycles).

During ion bombardment of a 100 L O₂ exposed Ni surface these different binding states occur in a reversed order of succession. O₂-flash signals at 400 and 1100 K, related to drastic changes in secondary ion emission at 400, 700, and 1100 K, reflect the disappearance of various oxygen binding states. The exchange between different oxygen phases was studied by¹⁶O₂/¹⁸O₂ isotope experiments.     

Upper limit for thermal direct photon production in heavy-ion collisions at 60 and 200A·GeV

The production of direct photons has been investigated in reactions ofp and¹⁶O projectiles at 60 and 200A·GeV with C and Au nuclei. Photon and ⁰ spectra have been measured in the pseudorapidity range 1.52.1 for the transverse momentum region 0.4 GeV/cp _T 2.8 GeV/c employing the lead-glass spectrometer SAPHIR. An upper limit of 15% at the 90% confidence level for the direct photon signal relative to the neutral pion production is obtained from the comparison of measured photon spectra with Monte Carlo simulations of the hadronic background based on the reconstructed yield of ⁰ and mesons. Consequences for a possible phase transition to a quark-gluon plasma are discussed.     

Comment on “On the Anomalon Interpretation of 40Ar + Cu Collisions at 0.9 and 1.8 AGeV”

A recent article interpreted the experiment by Dersch et al. on the formation of ²⁴Na in ⁴⁰Ar + Cu interactions in a very simple manner. The results from emulsion experiments performed with 3.6 AGeV ²²Ne were adapted for the interpretation of the experiments with 1.8 AGeV ⁴⁰Ar. The model used the same mean value for the energy of minimum ionizing protons and pions at all angles. It is argued that a more complex approach is needed for a satisfactory interpretation.     

Transverse momentum distributions of neutral pions from central and peripheral16O+Au collisions at 200A·GeV

The production of neutral pions by the interaction of 200A·GeV p and¹⁶O projectiles with a Au target has been studied in the pseudorapidity range 1.5≦η≦2.1. Transverse momentum spectra have been measured between 0.4 GeV/c and 3.6 GeV/c and their dependence on the centrality of the collision has been investigated. The peripheral-collision spectra display a marked change of slope with a hard component starting at about 1.8 GeV/c, in contrast to central-collision data. The data are discussed in comparison to p+p and α+α data from the ISR.