Ein neuer Apparat zur volumetrischen Kohlenstoffbestimmung

Ohne Zusammenfassung     

Unusual Mn-Mn spin coupling in the polar intermetallic compounds CaMn2Sb2 and SrMn2Sb2

Large single-crystals of two polar intermetallic phases, CaMn2Sb2 and SrMn2Sb2, have been grown using In or Sn as metal fluxes and characterized by single-crystal X-ray diffraction. The two compounds are isostructural and crystallize with the CaAl2Si2 structure (space group P3m1, No. 164) with unit cell parameters determined at 120(2) K of a = 4.5204(6) angstroms, c = 7.456(2) angstroms and a = 4.5802(17) angstroms, c = 7.730(5) angstroms for CaMn2Sb2 and SrMn2Sb2, respectively. Temperature- and field-dependent dc- and ac-magnetization measurements suggest complex magnetic ordering of the Mn moments below ca. 250 and 35 K for CaMn2Sb2 and below ca. 265 K for SrMn2Sb2. Resistivity measurements reveal metallic-like temperature dependence with rho(290) = 40 m omega cm for CaMn2Sb2 and rho290 = 100 m omega cm for SrMn2Sb2 with negligible magnetoresistance at 5 K in applied magnetic fields up to 10 kOe. Spin-polarized DFT electronic structure calculations confirm the metallic-like properties and provide further evidence for a magnetic structure where Mn atoms form two magnetic sublattices with ferromagnetic coupling within them and strong antiferromagnetic coupling between them.     

Theoretical study on the repair mechanism of the (6-4) photolesion by the (6-4) photolyase

UV irradiation of DNA can lead to the formation of mutagenic (6-4) pyrimidine-pyrimidone photolesions. The (6-4) photolyases are the enzymes responsible for the photoinduced repair of such lesions. On the basis of the recently published crystal structure of the (6-4) photolyase bound to DNA [Maul et al. 2008] and employing quantum mechanics/molecular mechanics techniques, a repair mechanism is proposed, which involves two photoexcitations. The flavin chromophore, initially being in its reduced anionic form, is photoexcited and donates an electron to the (6-4) form of the photolesion. The photolesion is then protonated by the neighboring histidine residue and forms a radical intermediate. The latter undergoes a series of energy stabilizing hydrogen-bonding rearrangements before the electron back transfer to the flavin semiquinone. The resulting structure corresponds to the oxetane intermediate, long thought to be formed upon DNA-enzyme binding. A second photoexcitation of the flavin promotes another electron transfer to the oxetane. Proton donation from the same histidine residue allows for the splitting of the four-membered ring, hence opening an efficient pathway to the final repaired form. The repair of the lesion by a single photoexcitation was shown not to be feasible.     

A test of special relativity with stored lithium ions

Laser spectroscopy at the heavy ion storage ring TSR in Heidelberg allows for precision experiments testing the limits of the special theory of relativity. With an optical-type three-level system of⁷Li⁺ the Doppler shift has been measured by saturation spectroscopy as a test of the time dilatation factor = (1 – ²)^–1/2 at an ion velocity of = 6.4% c. A precision of/ < 9 × 10^–9 has been obtained, which sets a second-order limit of 1.1 × 10^–6 for any deviation from the time dilatation factor. The fourth-order limit of this deviation is set below 2.7 × 10^–4 by the present experiment. These limits are given at a 1 confidence level.