Separation of Dihydro-Isocoumarins and Dihydro-Stilbenoids from Hydrangea macrophylla ssp. serrata by Use of Counter-Current Chromatography

Previously, different Hydrangea macrophylla ssp. serrata cultivars were investigated by untargeted LC-MS analysis. From this, a list of tentatively identified and unknown compounds that differ significantly between these cultivars was obtained. Due to the lack of reference compounds, especially for dihydro-isocoumarins, we aimed to isolate and structurally characterise these compounds from the cultivar ‘Yae-no-amacha’ using NMR and LC-MS methods. For purification and isolation, counter-current chromatography was used in combination with reversed-phase preparative HPLC as an orthogonal and enhanced purification workflow. Thirteen dihydro-isocoumarins in combination with other metabolites could be isolated and structurally identified. Particularly interesting was the clarification of dihydrostilbenoid glycosides, which were described for the first time in H. macrophylla ssp. serrata. These results will help us in further studies on the biological interpretation of our data.     

Multivalency as a Chemical Organization and Action Principle

Multivalent interactions can be applied universally for a targeted strengthening of an interaction between different interfaces or molecules. The binding partners form cooperative, multiple receptor–ligand interactions that are based on individually weak, noncovalent bonds and are thus generally reversible. Hence, multi‐ and polyvalent interactions play a decisive role in biological systems for recognition, adhesion, and signal processes. The scientific and practical realization of this principle will be demonstrated by the development of simple artificial and theoretical models, from natural systems to functional, application‐oriented systems. In a systematic review of scaffold architectures, the underlying effects and control options will be demonstrated, and suggestions will be given for designing effective multivalent binding systems, as well as for polyvalent therapeutics.     

Diffractive proteon fragmentation in 16, 32, and 110 GeV/cK − p interactions and the diffractive production of heavy quarks(s\bar s,c\bar c)

The inclusive proton diffraction dissociation cross sections in 16, 32, and 110 GeV/cK ^? p interactions are determined from the spike nearx=1 in the inclusive negative particle spectra and are compared to those obtained inK?p interactions using other selection methods at various energies. The same procedure is applied to events containing aV ⁰ in order to obtain the cross section for diffractive \(s\bar s\) production. While the total cross section for proton diffraction is found to be approximately constant in the energy range studied here, proton diffraction yielding an \(s\bar s - pair\) is found to increase significantly. In particular it is almost constant at 85 μb forΛ ⁰ and Σ production but for \(NK\bar K\) it rises from zero at 16 GeV.c to about 200 μb at 110 GeV/c. From the result for \(s\bar s\) diffractive production an estimate for the \(c\bar c\) diffractive production cross section of approximately 1–10 μb at 110 GeV/c is obtained.     

Laserspektroskopie

X-Ray spectra and chemical binding     

Inclusive production of non-strange resonances inK − p interactions at 32 GeV/c

New data on the inclusive production of the non-strange resonances ?⁰(770), ω(783), ?(1020) andf(1270) inK ^? p interactions at 32 GeV/c are presented. The inclusive production cross sections are equal to (4.32±0.72) mb, (3.7±1.4) mb, (0.65±0.10) mb and (0.91±0.35) mb respectively. Estimates of the topological cross sections are also obtained. The invariant and non-invariantx-distributions for the vector mesons ?⁰ and ? indicate the prevalence of forward resonance production in the c.m. system. For the tensorf-meson the rapidity andx-distributions are presented. Thet′-distributions for ?⁰, ?, andf have exponential slopes of 0.6±0.1 GeV^?2, 1.2±0.2 GeV^?2, and 0.8±0.5 GeV^?2 respectively. The exponential slope ofp _T ² -distribution of thef-meson is equal to (2.3±0.5) GeV^?2.     

Ab initio predictions of zeolite structures and Si NMR chemical shifts

A recent shell-model potential parameterized on ab initio data is used for predicting the all-silica structures of zeolites MFI, MEI, MTW, TON, FAU and of α-quartz. Cluster models are defined around each site and the ²⁹Si NMR shielding constants are calculated by ab initio techniques (GIAO-HF). Good agreement with observed ²⁹Si NMR chemical shifts is found. Comparison is made with shifts calculated for observed structures. The structures predicted by the ab initio shell-model potential prove as accurate as the observed ones when judged on the quality of the calculated ²⁹Si NMR spectra.     

On‐chip THz spectrometer for bunch compression fingerprinting at fourth‐generation light sources

The layout of an integrated millimetre‐scale on‐chip THz spectrometer is presented and its peformance demonstrated. The device is based on eight Schottky‐diode detectors which are combined with narrowband THz antennas, thereby enabling the simultaneous detection of eight frequencies in the THz range on one chip. The size of the active detector area matches the focal spot size of superradiant THz radiation utilized in bunch compression monitors of modern linear electron accelerators. The 3 dB bandwidth of the on‐chip Schottky‐diode detectors is less than 10% of the center frequency and allows pulse‐resolved detection at up to 5 GHz repetition rates. The performance of a first prototype device is demonstrated at a repetition rate of 100 kHz at the quasi‐cw SRF linear accelerator ELBE operated with electron bunch charges between a few pC and 100 pC.