Hydrogen Bonds in Rubidium Amide‐Ammonia(3/2), RbNH2·2/3NH3

Rubidium amide‐ammonia(3/2), RbNH₂·2/3NH₃, was synthesized from Rubidiumhydride, RbH, in liquid ammonia at ?78 °C. The compound crystallizes in the cubic space group I2₁3 with Z = 4, a = 10.0490(12) Å, and V = 1014.77(20) Å as isometric colorless crystals. The crystal structure was solved from single‐crystal X‐ray data. The structure contains a three‐dimensional network of amide anions and ammonia molecules, which are interconnected via hydrogen bonds.     

Experimental Charge Density Studies of Cyclotetrasilazane and Metal Complexes Containing the Di‐ and Tetraanion

The homologous series of parent octamethylcyclotetrasilazane (c‐NH‐SiMe₂‐)₄, ( 1 ), the lithium complex [(THF)₂Li₂(c‐N‐SiMe₂‐NH‐SiMe₂‐)₂]₂, ( 2 ), containing the cyclic dianion, and [(THF)₂LiAl(c‐N‐SiMe₂‐)₄]₂, ( 3 ), accommodating the unprecedented tetraanion [Me₂SiN]^4‐ was synthesized to investigate the nature of the covalent Si‐N single bond in the presence of various metals. These model compounds show a wide diversity of Si‐N(H), Si‐N(M), Si‐N(H, M) and M‐N bonds and serve as bench‐mark systems to study polar bonds by high‐resolution low‐temperature X‐ray structure analysis. Experimental charge density studies reveal highly polar Si‐N bonds with remarkable ionic contribution, even in the non‐metallated starting material 1 . The Li‐N and Li‐O bonds have to be classified as almost purely ionic bonds with topological properties not far from those determined for NaCl.     

Investigation of high‐speed boundary‐layer transition by DNS

An investigation of hypersonic boundary‐layer flow along a flat plate is being presented. The high Mach number investigated calls for the consideration of the chemical reactions and the change in thermodynamical properties for temperatures up to T = 6000 K. For the current investigation a test case at M = 20 and the atmospheric conditions at an altitude of H = 50 Km is chosen. The differences to the ideal‐gas result is demonstrated. (© 2004 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)     

Time-resolved two-photon photoemission spectroscopy of HOPG and Ag nanoparticles on HOPG

Received: 6 November 1998     

Two stereoisomeric pentacyclic oxin­dole alkaloids from Uncaria tomentosa: uncarine C and uncarine E

The chloro­form solvate of uncarine C (pteropodine), (1′S,3R,4′aS,5′aS,10′aS)‐1,2,5′,5′a,7′,8′,10′,10′a‐octa­hydro‐1′‐methyl‐2‐oxospiro­[3H‐indole‐3,6′(4′aH)‐[1H]­pyrano­[3,4‐f]indolizine]‐4′‐carboxyl­ic acid methyl ester, C₂₁H₂₄N₂O₄·CHCl₃, has an absolute configuration with the spiro C atom in the R configuration. Its epimer at the spiro C atom, uncarine E (isopteropodine), (1′S,3S,4′aS,5′aS,10′aS)‐1,2,5′,5′a,7′,8′,10′,10′a‐octahydro‐1′‐methyl‐2‐oxospiro[3H‐indole‐3,6′(4′aH)‐[1H]pyrano[3,4‐f]indolizine]‐4′‐carboxylic acid methyl ester, C₂₁H₂₄N₂O₄, has Z′ = 3, with no solvent. Both form intermolecular hydrogen bonds involving only the ox­indole, with N?O distances in the range 2.759 (4)–2.894 (5) Å.     

Nachruf auf Philipp Furtwängler

Ohne ZusammenfassungGedächtnisrede, die der Verf. am 7. Juni 1940 in der Wiener Mathematischen Gesellschaft hielt.     

Ultrafast Internal Conversion in a Model Anthocyanin–Polyphenol Complex: Implications for the Biological Role of Anthocyanins in Vegetative Tissues of Plants

The red flavylium cations of anthocyanins form ground‐state charge‐transfer complexes with several naturally occurring electron‐donor copigments, such as hydroxylated flavones and hydroxycinnamic or benzoic acids. Excitation of the 7‐methoxy‐4‐methyl‐flavylium–protocatechuic acid complex results in ultrafast (240 fs) internal conversion to the ground state of the complex by way of a low‐lying charge‐transfer state. Thus, both uncomplexed anthocyanins, whose excited state decays by fast (5–20 ps) excited‐state proton transfer, and anthocyanin–copigment complexes have highly efficient mechanisms of deactivation that are consistent with the proposed protective role of anthocyanins against excess solar radiation in the vegetative tissues of plants.     

Amperometric lactate biosensors and their application in (sports) medicine, for life quality and wellbeing

The article reviews the use of electrochemical biosensors for detecting lactate, a key metabolite of the anaerobic glycolytic pathway. This compound plays an important role in (sports) medicine, in the nutritional sector, in food quality control and touches environmental concerns. Amperometric biosensors offer a sensitive and selective means to monitor organic analytes like lactate. A detailed study on different aspects of amperometric lactate biosensor preparation is described: the main configuration aspects are compiled regarding electrode materials, biorecognition elements, immobilization methods, mediators and cofactors as well as fields of application. Comparative studies are conducted correlating different configuration aspects and performance of the resulting biosensors. This review contains 214 references from the years 1974 to 2007. Correspondence: Beate Strehlitz, UFZ, Helmholtz Centre for Environmental Research – UFZ, Environmental and Biotechnology Centre (UBZ), Permoserstrasse 15, D-04318 Leipzig, Germany