High spin states in 74Se

Gamma-ray transitions from the bombardment of ⁶⁴Ni by ¹⁶O up to 81 Me V were studied in a variety of experiments. Four transitions in coincidence with four previously known transitions in ⁷⁴Se were discovered. Information on energies, angular distributions, intensities multiplicities and lifetimes is given for these transitions. Excitation functions for this and several other channels are presented. Statistical calculations are in satisfactory agreement with experiment.     

Heavy ion induced transfer reactions on 148Nd

Transfer reactions induced by ¹⁶O and ¹⁸O beams on ¹⁴⁸Nd were measured with a time-of-flight setup at 72 MeV incident energy. The angular distributions are bell shapes having their maxima at angles somewhat below the grazing angle. The excitation in the final nuclei takes place (if possible) near the optimum Q-value and is spread over 5 MeV for the one-particle transfer reactions and up to 10 MeV for the multiparticle transfers. The cross sections for the individual channels are explained mostly by Q-window considerations. In spite of the differences in the individual channels the total transfer cross section integrated over excitation energy, angle, and all channels turns out to be the same same for both ¹⁶O and ¹⁸O beams. This cross section amounts to 20 % of the total reaction cross section and nicely fills the gap between the measured fusion cross section and the total reaction cross section obtained from optical model calculations based on elastic scattering data.     

Synthesis and Structure of Ba7F12Cl2

Crystals of ordered and disordered Ba₇F₁₂Cl₂ were prepared by flux growth and solid state reactions. These new structures were characterized by single crystal and powder X‐ray diffraction. The disordered variant which shows disorder on one of the cation sites was obtained from a BaF₂ + BaCl₂ + NaCl/NaF flux. It has hexagonal space group P6₃/m (176) with one formula unit per unit cell. The lattice constants are a = b = 1059.55(5) pm and c = 420.10(4) pm (at 21 °C). The structure was refined to R(R_w) = 0.026(0.030) for 346 independent reflections and 26 parameters. Slow cooling of a mixture of BaF₂ and LiCl yields the ordered variant. This one crystallizes in the hexagonal space group P6 (174) with one formula per unit cell. Lattice constants at 21 °C are a = b = 1063.46(2) pm and c = 417.52(1) pm. The structure was refined to R(R_w) = 0.017 (0.017) for 638 independent reflections and 45 parameters. The structural arrangement and the interatomic distances of the two variants are mutually similar. The barium atoms have coordination number nine. Propeller‐type arrangements with a chloride ion on the axis and the fluoride ions as blades are observed. These latter ones are interconnected into ‘channels' of tricapped fluoride prisms. Occupation disorder of the barium sites in the channels of the disordered variant makes the main difference between the two. An unexpectedly high X‐ray density obtained for both variants of Ba₇F₁₂Cl₂ can be correlated to the density of other barium fluorohalides having a coordination number of nine for the barium ion.     

Boron Hydrogen Compounds: Hydrogen Storage and Battery Applications

About 25 years ago, Bogdanovic and Schwickardi (B. Bogdanovic, M. Schwickardi: J. Alloys Compd. 1–9, 253 (1997) discovered the catalyzed release of hydrogen from NaAlH₄. This discovery stimulated a vast research effort on light hydrides as hydrogen storage materials, in particular boron hydrogen compounds. Mg(BH₄)₂, with a hydrogen content of 14.9 wt %, has been extensively studied, and recent results shed new light on intermediate species formed during dehydrogenation. The chemistry of B₃H₈⁻, which is an important intermediate between BH₄⁻ and B₁₂H₁₂²⁻, is presented in detail. The discovery of high ionic conductivity in the high-temperature phases of LiBH₄ and Na₂B₁₂H₁₂ opened a new research direction. The high chemical and electrochemical stability of closo-hydroborates has stimulated new research for their applications in batteries. Very recently, an all-solid-state 4 V Na battery prototype using a Na₄(CB₁₁H₁₂)₂(B₁₂H₁₂) solid electrolyte has been demonstrated. In this review, we present the current knowledge of possible reaction pathways involved in the successive hydrogen release reactions from BH₄⁻ to B₁₂H₁₂²⁻, and a discussion of relevant necessary properties for high-ionic-conduction materials.     

Rotational bands in 167Hf

High-spin states in ¹⁶⁷Hf, populated in the ¹⁴¹Pr(³⁰Si, p3n)¹⁶⁷Hf reaction, have been studied using the nordball Ge detector array. Three rotational cascades have been observed for the first time and the previously-known level scheme has been extended to significantly higher spin. Band-crossing effects are discussed within the framework of Woods-Saxon cranking calculations and are found to be in good agreement. Received: 9 April 1999 / Revised version: 13 May 1999     

Subhertz-linewidth infrared frequency source with a long-term instability below 5 × 10−15

Distributing a stable, absolute optical reference frequency via fiber network would serve research and development in academia and industry. Lasers stabilized to high-finesse Fabry–Pérot cavities can achieve fractional frequency instabilities of less than 10^?15 for periods up to several seconds. Their instabilities increase for longer averaging times due to a variable frequency drift, with a linear drift component of the order of 10…100 mHz/s. Hydrogen masers, on the other hand, yield an instability floor of a few parts in 10^?15, but suffer from poor stabilities on short timescales. We demonstrate an infrared optical frequency source that combines a cavity-stabilized laser with a hydrogen maser to achieve a residual fractional frequency instability better than 5 × 10^?15 for all averaging times from 0.4 up to 10,000 s. The frequency drift of the system over a period of 40,000 s is less than 30 µHz/s. For obtaining absolute frequency accuracy, the hydrogen maser is referenced to a primary frequency standard.     

DNA binding and nuclease activity of a water-soluble sulfonated manganese(III) corrole

The interaction of a water-soluble sulfonated Mn(III) corrole Mn(tpfc)(SO₃Na)₂ [tpfc = 5,10,15-tris(pentafluorophenyl)corrole] with calf thymus DNA (ct-DNA) has been studied by spectroscopic methods, and the nuclease activity of this complex has also been examined by agarose gel electrophoresis. Mn(tpfc)(SO₃Na)₂ exhibits weak aggregation tendency in buffer solution and can bind to ct-DNA via an outside binding mode with a binding constant of 1.25 × 10⁴ M^?1. The observed increase in Stern–Volmer quenching constant with increasing temperature indicates that the competition of the manganese corrole and ethidium bromide with ct-DNA is a dynamic process. Moreover, the manganese corrole displays good chemical nuclease activity in the presence of hydrogen peroxide via oxidative cleavage of DNA.     

间位苯基桥联的锰(Ⅲ)双咔咯的合成、表征及催化氧化性质(英文)

通过间苯二甲醛与5-氟苯基二吡咯甲烷反应合成了一种新的间位苯基桥联的双咔咯1,并利用锰盐与自由咔咯反应制备了其锰的金属配合物2。采用紫外、质谱、核磁、XPS等手段对化合物进行了表征。以苯乙烯为底物考察了锰双咔咯2的催化氧化性质,探讨了时间、溶剂、氧源、轴向配体对催化反应的影响。结果表明以亚碘酰苯和间氯过氧苯甲酸为氧源时催化的主要产物为环氧苯乙烷,而以双氧水和叔丁基过氧化氢为氧源时则主要产物为苯甲醛;在极性溶剂中的催化氧化产率较高。轴向配体对催化氧化有促进作用,不同轴向配体对催化反应产率提高的顺序是:1-甲基咪唑吡啶咪唑。     

Transition to non-collective states at high spin in 124Xe

Excited states in ¹²⁴Xe were populated in the reaction ⁸²Se(⁴⁸Ca, 6n)¹²⁴Xe and γ -ray coincidence relationships were measured with the Gammasphere spectrometer. Two new bands are observed and several of the previously known bands are extended in the high- as well as in the low-spin region. Two irregular high-spin structures are also added. The irregularities are a fingerprint of a transition from collective to non-collective behaviour. Configuration assignments to the new structures are proposed on the basis of systematics and by comparing experimental properties with calculations within the framework of the cranking model.