Mikrochemie

Ohne Zusammenfassung     

Partition numbers

We continue [21] and study partition numbers of partial orderings which are related to (ω)/fin. In particular, we investigate P_f, be the suborder of ((ω)/fin)^ω containing only filtered elements, the Mathias partial order M, and (ω), (ω)^ω the lattice of (infinite) partitions of ω, respectively. We show that Solomon's inequality holds for M and that it consistently fails for P_f. We show that the partition number of (ω) is C. We also show that consistently the distributivity number of (ω)^ω is smaller than the distributivity number of (ω)/fin. We also investigate partitions of a Polish space into closed sets. We show that such a partition either is countable or has size at least D, where D is the dominating number. We also show that the existence of a dominating family of size ₁ does not imply that a Polish space can be partitioned into ₁ many closed sets.     

Reinstallation of the COMPASS-D tokamak in IPP ASCR

The COMPASS-D tokamak, originally operated by UKAEA at Culham, UK, will be reinstalled at the Institute of Plasma Physics (IPP) AS CR. The COMPASS device was designed as a flexible tokamak in the 1980s mainly to explore the MHD physics. Its operation (with D-shaped vessel) began at the Culham Laboratory of the Association EURATOM/ UKAEA in 1992.The COMPASS-D tokamak will have the following unique features after putting in operation on IPP Prague. It will be the smallest tokamak with a clear H-mode and ITER-relevant geometry. ITER-relevant plasma conditions will be achieved by installation of two neutral beam injection systems (2 × 300 kW), enabling co-and counter-injections. Redeployment of the existing LH system (400 kW) is also envisaged. A comprehensive set of diagnostics focused mainly on the edge plasma will be installed.The scientific programme proposed for the COMPASS-D tokamak installed in IPP Prague will benefit from these unique features of COMPASS-D and consist of two main scientific projects, both highly relevant to ITER-Edge plasma physics (H-mode studies) and Wave-plasma interaction studies.The COMPASS-D tokamak will offer an important research potential as a small, flexible and low-cost facility with ITER-relevant geometry.     

Few-valence-particle excitations around doubly magic 132Sn

Prompt γ-ray cascades in neutron-rich nuclei around doubly-magic ¹³²Sn have been studied using a ²⁴⁸Cm fission source. Yrast states located in the N = 82 isotones ¹³⁴Te and ¹³⁵I are interpreted as valence proton and neutron particle-hole core excitations with the help of shell model calculations employing empirical nucleon-nucleon interactions from both ¹³²Sn and ²⁰⁸Pb regions.     

Study of spontaneous fission with EUROGAM

Prompt γ radiation following spontaneous fission has been measured using the EUROGAM 2 array. Using these data and newly developed analysis techniques a number of subjects were studied, which are briefly discussed. One of these subjects, shape transition in A≈100 Sr and Zr nuclei is discussed in more detail. Quadrupole moments were determined for rotational bands in the N=58,59,60,62 and 64 Sr and Zr isotopes. Deformation parameters, which increase from β₂ ≈ 0.1 at N=56 to β₂ ≈ 0.4 at N=64, suggest that in strontium and zirconium isotopes shape change happens gradually between N=56 and N=62 and is probably due to an occupancy of three or more deformation-driving orbitals of h_11/2 parentage.     

Relating neural dynamics to neural coding

We demonstrate that two key theoretical objects used widely in computational neuroscience, the phase-resetting curve (PRC) from dynamics and the spike triggered average (STA) from statistical analysis, are closely related when neurons fire in a nearly regular manner and the stimulus is sufficiently small. We prove that the STA due to injected noisy current is proportional to the derivative of the PRC. We compare these analytic results with numerical calculations for the Hodgkin-Huxley neuron and we apply the method to neurons in the olfactory bulb of mice. This observation allows us to relate the stimulus-response properties of a neuron to its dynamics, bridging the gap between dynamical and information theoretic approaches to understanding brain computations and facilitating the interpretation of changes in channels and other cellular properties as influencing the representation of stimuli.     

Preparation of quaternary pyridinium salts as possible proton conductors

On basis of earlier experimental experience, the transfer of protons in salts of the organic cation-inorganic anion type occurs primarily through directional arrangement of the anion-anion type short hydrogen bonds. The submitted work presents the preparation of quaternary pyridinium salts of inorganic hydrogen anions in the absence of solvent molecules in their crystal structure. These substances can form only the above-described anion-anion type hydrogen bonds; in addition, the absence of solvate anions increases the stability of the prepared compounds. A total of six substituted pyridinium salts were prepared, four of which have not been described yet: 1,2,4,6-tetraphenylpyridinium perchlorate, 1-benzyl-2,4,6-trimethylpyridinium perchlorate, 1,4-dimethylpyridinium hydrogen sulphate, 1,4-dimethylpyridinium dihydrogen phosphate, 1,4-dimethylpyridinium hydrogen sulphate, and 1,2-dimethyl-5-ethylpyridinium dihydrogen phosphate. Three of these substances were characterised by X-ray structural analysis: 1,2,4,6-tetraphenylpyridinium perchlorate crystallises in the orthorhombic system, space group Pbca; 1-benzyl-2,4,6-trimethylpyridinium perchlorate crystallises in the monoclinic system, space group P2₁/c; and 1,4-dimethylpyridinium dihydrogen phosphate crystallises in the monoclinic system, space group C2/c. This structure contains an oriented anion network bond by short anion-anion type hydrogen bonds with the donor acceptor lengths of 2.567(3) Å and 2.557(3) Å and thus fulfils the requirements of a good proton conductor.     

Cycloaddition Reactions of Deoxyribosylpropynoates

Pure anomers of either α or β 3-(2-deoxyribofuranosyl)propynoates reacted with the tetramethylcyclobutadiene–aluminum trichloride complex to yield the corresponding diastereoisomeric Dewar benzenes. Thermal- or ultraviolet light–initiated rearrangement gave rise to highly substituted C-aryldeoxyribosides as single anomers. The same compounds as well as other substituted deoxyribosides were obtained also by transition metal–mediated cycloaddition reactions.