Photoproduction of η -mesons off protons

Photoproduction of η -mesons was studied with the Crystal-Barrel detector at ELSA for photon energies in the range from 0.75 to 3GeV. Total and differential cross-sections are presented. The η mesons are detected in two decay modes, in η → 2γ and in η → 3π⁰ → 6γ . The cross-sections vary slowly as functions of energy and η production angle suggesting that only few resonances make significant contributions to the cross-section. For photon energies above 1.5GeV, the differential cross-sections show a strong forward peak due to meson exchanges in the t channel. A comparison of the η -photoproduction cross-sections with SAID and MAID as well as with a partial-wave analysis performed on our data in combination with other data sets shows good agreement. The Bonn-Gatchina partial-wave analysis suggests that the largest contribution to η photoproduction for energies below 3GeV proceeds via three resonances, the well-known N(1535)S ₁₁ , via N(1720)P ₁₃ , and a newly suggested N(2070)D ₁₅ .     

The Structure of the Aluminum Fumarate Metal–Organic Framework A520

The synthesis of the commercially available aluminum fumarate sample A520 has been optimized and its structure analyzed through a combination of powder diffraction, solid‐state NMR spectroscopy, molecular simulation, IR spectroscopy, and thermal analysis. A520 is an analogue of the MIL‐53(Al)‐BDC solid, but with a more rigid behavior. The differences between the commercial and the optimized samples in terms of defects have been investigated by in situ IR spectroscopy and correlated to their catalytic activity for ethanol dehydration.     

Universal Approach Towards r‐Hirudin Derivatives with High Anti‐Thrombin Activity Based on Chemical Differentiation of Primary Amino Groups

Chemical modification of recombinant hirudin (r‐hirudin) is necessary whenever surface‐confinement to a biomaterial or biotinylation for subsequent conjugation with carriers is intended. Here, we report a modification strategy that permits chemical discrimination between r‐hirudin's amino groups and preserves its thrombin inhibitor activity. By reaction with Msc‐ONSu, protective groups were successively introduced in r‐hirudin yielding four derivatives (Msc)_x‐hirudin (1 ≤ x ≤ 4) and pure fractions were isolated by ion exchange chromatography. Structure–function relationships were studied for all derivatives and revealed a decrease in activity of more than 90% as compared to unprotected r‐hirudin. MALDI‐TOF MS was used to determine the locations of the Msc groups. Furthermore, evidence was provided that r‐hirudin's N‐terminal amino group is highly important for its anti‐thrombin activity. Selective modification of the lysine residues which maintained the free N‐terminal amino group preserved the anti‐thrombin activity of r‐hirudin even after biotinylation and subsequent linkage to streptavidin or confinement to a polymer surface.     

Routine analysis of ultra pure water by ICP-MS in the low- and sub-ng/L level

The chemical analysis with inductively coupled plasma-mass spectrometry (ICP-MS) can help to examine the purity of ultra pure water (UPW) down to 10 part per trillion (ng/L) and lower. For a proper determination of a high number of samples per week the analysis must be divided into two parts: the routine analysis and the reference water analysis. The routine analysis is done by direct measurement of the ultra pure water samples. Applying a standard addition method under particular clean conditions, the reference water analysis leads to the definition of the accurate zero. A quick evaluation scheme is also presented for the reference water analysis. The method is tested for its fitness for application by examining LOD (for relevant element < 2 ng/L), reproducibility and linearity of calibration. The ICP-MS was optimized according to the methodology of G. Taguchi to improve reproducibility and LOD. Received: 16 June 1999 / Revised: 2 August 1999 / Accepted: 6 August 1999     

Dual catalysis: combining photoredox and Lewis base catalysis for direct Mannich reactions

A dual catalytic system combining photoredox and Lewis base catalysis has been developed. By the appropriate choice of light source and catalyst, the photoredox cycle can be optimally modulated to match the base catalyzed reaction cycle to provide the corresponding products under mild reaction conditions.     

CH Functionalization of Phenols Using Combined Ruthenium and Photoredox Catalysis: In Situ Generation of the Oxidant

A combination of ruthenium and photoredox catalysis allowed the ortho olefination of phenols. Using visible light, the direct C? H functionalization of o‐(2‐pyridyl)phenols occurred, and diverse phenol ethers were obtained in good yields. The regeneration of the ruthenium catalyst was accomplished by a photoredox‐catalyzed oxidative process.     

MeV-boron implanted layer, oxygen precipitates and poly-silicon back side combined in one silicon wafer: at what defect will Cu and Ni be gettered?

We have measured the gettering efficiencies for Cu and Ni of various silicon wafers, such as MeV-boron-implanted p- polished wafers treated with two different implantation doses of 3×10¹³ atoms/cm² B and 1×10¹⁵ atoms/cm² B, respectively. A third kind of wafer was covered with a poly-silicon back side and thermally pretreated before the gettering test to form oxygen precipitates in the bulk. The gettering test started with a reproducible spin-on spiking on the front side of the wafers in the range around 10¹² atoms/cm², followed by a thermal treatment to redistribute the metallic impurities in the wafer. Then the gettering efficiencies were measured by a novel wet chemical layer-by-layer etching technique in combination with inductively coupled plasma mass spectrometry. This led to “stratigraphical concentration profiles” of the metallic impurities in the wafer with typical detection limits of (5–10)×10¹² atoms/cm³. The concentration profiles were compared with concentration profiles found after testing the gettering efficiency of p/p+ epitaxial wafers. Almost 100% of the total intentional Cu spiking was recovered in the boron buried layer for both implantation doses. On the front surface and in the region between the front surface and the buried layer a Cu concentration ∼20 times higher than on/in p/p+ epitaxial wafers/layers was measured for the implanted specimen. The lower implantation dose led to higher Cu-concentration levels on the front surface compared to the higher implantation dose. The wafer containing a MeV-boron-implanted layer as well as oxygen precipitates and a poly-silicon back side exhibited a Cu distribution of 30/∼0/70%, respectively. Thus, the gettering by poly-silicon exceeded both the gettering effects by the buried layer and by the oxygen precipitates. Ni gettering in MeV-boron-implanted wafers exhibited other characteristics. The gettering efficiency of the buried layer was 65%, while the remaining Ni contamination was equally distributed between the front-side region and the wafer back side. A wafer containing a buried layer obtained by a 1×10¹⁵ atoms/cm³ B dose and oxygen precipitates exhibited 17% of the total Ni contamination in the boron layer, while ∼80% of the total Ni contamination was gettered by oxygen precipitates. In the case of buried layer/oxygen precipitates/poly-silicon back side the distribution was found to be 13/37/45%, thus exhibiting equal gettering strengths for oxygen precipitates and the poly-silicon back side for Ni contamination. The results were discussed in terms of segregation and relaxation-induced gettering mechanisms including different reaction rates. Received: 30 May 2001 / Accepted: 16 June 2001 / Published online: 30 August 2001