The Laughlin liquid in an external potential

We study natural perturbations of the Laughlin state arising from the effects of trapping and disorder. These are N-particle wave functions that have the form of a product of Laughlin states and analytic functions of the N variables. We derive an upper bound to the ground state energy in a confining external potential, matching exactly a recently derived lower bound in the large N limit. Irrespective of the shape of the confining potential, this sharp upper bound can be achieved through a modification of the Laughlin function by suitably arranged quasi-holes.     

Impact of ice particle shape on short-wave radiative forcing: A case study for an arctic ice cloud

We used four different non-spherical particle models to compute optical properties of an arctic ice cloud and to simulate corresponding cloud radiative forcings and fluxes. One important finding is that differences in cloud forcing, downward flux at the surface, and absorbed flux in the atmosphere resulting from the use of the four different ice cloud particle models are comparable to differences in these quantities resulting from changing the surface albedo from 0.4 to 0.8, or by varying the ice water content (IWC) by a factor of 2. These findings show that the use of a suitable non-spherical ice cloud particle model is very important for a realistic assessment of the radiative impact of arctic ice clouds. The differences in radiative broadband fluxes predicted by the four different particle models were found to be caused mainly by differences in the optical depth and the asymmetry parameter. These two parameters were found to have nearly the same impact on the predicted cloud forcing. Computations were performed first by assuming a given vertical profile of the particle number density, then by assuming a given profile of the IWC. In both cases, the differences between the cloud radiative forcings computed with the four different non-spherical particle models were found to be of comparable magnitude. This finding shows that precise knowledge of ice particle number density or particle mass is not sufficient for accurate prediction of ice cloud radiative forcing. It is equally important to employ a non-spherical shape model that accurately reproduces the ice particle's dimension-to-volume ratio and its asymmetry parameter. The hexagonal column/plate model with air-bubble inclusions seems to offer the highest degree of flexibility.     

A positron remoderator for the high intensity positron source NEPOMUC

A remoderator for the high intensity positron source NEPOMUC was developed and installed at the beam facility. A beam of remoderated positrons could be produced with different energies and a diameter of less than 2 mm was obtained. The efficiency of the remoderation setup was determined to be 5%. Due to the brilliance of the remoderated beam, the measurements at the coincidence Doppler broadening spectrometer (CDBS) and at the positron annihilation induced Auger electron spectrometer (PAES) could be improved. The setup and functionality of the remoderation device is presented as well as the first measurements at the remoderator, CDBS and PAES.     

Biadhesive Peptides for Assembling Stainless Steel and Compound Loaded Micro‐Containers

Biadhesive peptides (peptesives) are an attractive tool for assembling two chemically different materials—for example, stainless steel and polycaprolactone (PCL). Stainless steel is used in medical stents and PCL is used as a biodegradable polymer for fabrication of tissue growth scaffolds and drug delivering micro‐containers. Biadhesive peptides are composed of two domains (e.g., dermaseptin S1 and LCI) with different material‐binding properties that are separated through a stiff peptide‐spacer. The peptesive dermaseptin S1‐domain Z‐LCI immobilizes antibiotic‐loaded PCL micro‐containers on stainless steel surfaces. Immobilization is visualized by microscopy and field emission scanning electron microscopy analysis and released antibiotic from the micro‐containers is confirmed through growth inhibition of Escherichia coli cells.     

Design and synthesis of spirocyclic ligands of glucocorticoid receptors

Spirocyclic indazoles were designed as potential ligands for the glucocorticoid receptors (GRs). A short and efficient synthetic sequence was developed allowing the preparation of pure diastereomeric spirocyclic analogs of fluorocortivazol. Our studies also revealed a new application of Burgess reagent leading to a ring expansion. The structures and conformations of several key intermediates and products were confirmed by single crystal X-ray diffraction analysis. Conformational assignments were also supported by DFT calculations. As a proof of concept we tested the affinity of diastereomeric compounds 13b and 14b for the GRs. Rewardingly, it was found that 14b showed a promising IC₅₀ of 27?nM.     

Deoxytrifluoromethylthiolation and Selenylation of Alcohols by Using Benzothiazolium Reagents

Aliphatic compounds substituted with medicinally important trifluoromethylthio (SCF₃) and trifluoromethylselenyl (SeCF₃) groups were synthesized directly from alcohols by using the new benzothiazolium salts BT-SCF₃ and BT-SeCF₃ . These bench-stable fluorine-containing reagents are facile to use and can be prepared in two steps from non-fluorinated heteroaromatic starting materials. The metal-free deoxytrifluoromethylthiolation process using BT-SCF₃ proceeds under mild conditions and the similarly efficient trifluoromethylselenylation reactions using BT-SeCF₃ are, to the best of our knowledge, the first reported examples of this transformation.     

Towards Identification of Essential Structural Elements of Organoruthenium(II)-Pyrithionato Complexes for Anticancer Activity

An organoruthenium(II) complex with pyrithione (2-mercaptopyridine N-oxide) 1 a has previously been identified by our group as a compound with promising anticancer potential without cytotoxicity towards non-cancerous cells. To expand the rather limited research on compounds of this type, an array of novel chlorido and 1,3,5-triaza-7-phosphaadamantane (pta) organoruthenium(II) complexes with methyl-substituted pyrithiones has been prepared. After thorough investigation of the aqueous stability of these complexes, their modes of action have been elucidated at the cellular level. Minor structural alterations in the ruthenium-pyrithionato compounds resulted in fine-tuning of their cytotoxicities. The best performing compounds, 1 b and 2 b , with a chlorido or pta ligand bound to ruthenium, respectively, and a methyl group at the 3-position of the pyrithione scaffold, have been further investigated. Both compounds trigger early apoptosis, induce the generation of reactive oxygen species and G1 arrest in A549 cancer cells, and show no strong interaction with DNA. However, only 1 b also inhibits thioredoxin reductase. Wound healing assays and mitochondrial function evaluation have revealed differences between these two compounds at the cellular level.