Carbon Species and Precise Elemental Analysis of Precursors for Superconducting (Bi,Pb)2Sr2Ca2Cu3Ox Tapes

 The chemical composition of BiPbSrCaCuO precursors prepared by different syntheses has to be checked analytically before further application to production of superconducting (Bi,Pb)₂Sr₂Ca₂Cu₃O_x tapes. Carbon species in concentrations below 0,1%(w/w) were observed to be possibly a source of gas evolving reactions during the heat treatment procedures for the superconducting phase formation. A method that allows the temperature controlled detection of CO₂ resulting from reactions of various carbon species was developed based on an commercial C/H₂O-analyser with IR gas detectors. By means of this method it is possible to relate the carbon content to the conditions of synthesis and technological steps of the tape production. The phase formation mechanism of the superconducting (Bi,Pb)2223 phase from a multiphase precursor strongly depends on its elemental composition. Titrimetric and ICP spectrometric methods that allow the determination of the content of the main components Bi, Pb, Ca, Sr, and Cu with high precision and accuracy were developed and their results were compared. The best results were obtained with a combined chemical-spectrometric procedure. The relative standard deviations (RSD) for all metallic elements do not exceed 1%. The analytical results of the main components and specific trace determinations are essential for the functioning of superconducting tapes.     

The preparation of a cabbage reference material for environmental monitoring and food analysis

 Cabbage is frequently used in environmental monitoring and food control, and, hence, cabbage reference materials (RMs) are required for ensuring quality assurance. A cabbage RM was prepared in view of certification of specific elements from the "black list" of high toxicological interest and nutritive importance. All tasks of the RM production (production of the plant material, cutting and freeze-drying, determination of the residual water content, preparation of the RM, homogeneity testing, stability testing, certification measurements) are described in detail. Received: 12 November 1999 / Accepted: 29 January 2000     

Electron Beam‐Based Functionalization of Poly(ethersulfone) Membranes

Poly(ethersulfone) membranes were surface modified in a one‐step procedure. For this purpose, the membranes were soaked with aqueous solutions of different low‐molecular weight molecules bearing diverse hydrophilic functionalities and subject to electron beam treatment. No catalysts, photoinitiators, organic solvents or other toxic reagents were used, and no additional synthetic or purification steps were required.

     

Engyodontochones,Antibiotic Polyketides from the Marine Fungus Engyodontium album Strain LF069

Six new ( 2 , 4 – 8 ) and two known polyketides with a basic structure of an anthraquinone‐xanthone were isolated from mycelia and culture broth of the fungus Engyodontium album strain LF069. The structures and relative configurations of these compounds were established by spectroscopic means, and their absolute configurations were defined mainly by comparison of quantum chemical TDDFT calculated and experimental ECD spectra. Compounds 2 and 4 – 8 were given the trivial names engyodontochone A ( 2 ) and B–F ( 4 – 8 ). Compounds 5 – 8 represent the first example of a 23,28 seco‐beticolin carbon skeleton. The relative and absolute configurations of two known substances JBIR‐97/98 ( 1 ) and JBIR‐99 ( 3 ) were determined for the first time. All isolated compounds were subjected to bioactivity assays. Compounds 1 – 4 exhibited inhibitory activity against methicillin‐resistant Staphylococcus aureus (MRSA) that was 10‐fold stronger than chloramphenicol.     

Double Pancake Versus Long Chalcogen–Chalcogen Bonds in Six‐Membered C,N,S‐Heterocycles

The double “pancake” bonding in the dimers of the six‐membered heterocycles 1,3‐dithia‐2,4,6‐triazine ( 4 ) and 1,3‐dithia‐2,4‐diazine ( 16 ) were investigated by means of high‐level quantum chemical calculations (B3LYP and CCSD(T)). It was found that the S–S dimers, 20 a and 27 , are not the most stable isomers, but the dimers showing short S?N ( 21 a ) and S?C ( 25 , 28 ) bonds. An investigation of the 5‐phenyl‐1,3‐dithia‐2,4,6‐triazine ( 4 b ) yields that the syn dimer with two S?S bonds (2.57 Å) is the most stable one. In this dimer, the phenyl groups are placed on top of each other. The additional dispersion energy of the phenyl rings causes a stabilization of the syn‐S–S (C_2v‐like) isomer. As a result, two weak albeit relevant single S?S bonds (2.57 Å) are predicted. These findings contradict the recently published concept of double “pancake” bonding in the dimer 4 b ₂.     

Thuggacins, macrolide antibiotics active against Mycobacterium tuberculosis: isolation from myxobacteria, structure elucidation, conformation analysis and biosynthesis

Two novel antibiotics, thuggacin A (1) and B (2), were isolated from the myxobacterium Sorangium cellulosum. 1 and 2 are unique thiazole-containing macrolides with side chains on both sides of the lactone group. Upon standing in solution, thuggacin A (1) rearranges by acyl migration of the lactone group to give a mixture with thuggacins B (2) and C (3). NOEs and vicinal coupling constants within the lactone ring provided distinct data for the generation of a structure model by PM3 calculations, which allowed an analysis of the conformation in solution and the relative configuration of six asymmetric centres. A minor sorangium metabolite was identified as 13-methyl-thuggacin A (4). Furthermore, two natural thuggacin variants, 5 and 6, were found in another myxobacterium, Chondromyces crocatus. In these variants, one side chain is replaced by a methyl group and a hydroxy group is repositioned to give a primary alcohol at the former methyl site, in an alpha position with respect to the thiazole ring. 1 proved to be active against clinical isolates and reference strains of Mycobacterium tuberculosis. Preliminary studies on the mechanism of action indicate inhibition of the cellular electron-transport chain.     

Changes in microbial community structure and function within particle size fractions of a paddy soil under different long-term fertilization treatments from the Tai Lake region, China

Greenhouse gas (GHG) production and emission from paddy soils impacts global climate change. Soil particle size fractions (PSFs) of different sizes act as soil microhabitats for different kinds of microbial biota with varying conditions of redox reactions and soil organic matter (SOC) substrates. It is crucial to understand the distribution of soil microbial community structure within PSFs and linkage to the GHG production from paddy soils of China. The change of bacterial and methangenic archaeal community and activity relating to CH₄ and CO₂ production with PSFs under different fertilizer applications was studied in this paper. The fertilization trial was initiated in a paddy soil from the Tai Lake region, Jiangsu, China with four treatments of non-fertilized (NF), fertilized with inorganic fertilizers only (CF), inorganic with pig manure (CFM) and inorganic with straw return (CFS), respectively since 1987, and the PSFs (<2 μm, 2–20 μm, 20–200 μm, and 200–2000 μm) were separated by a low energy sonication dispersion procedure from undisturbed samples. Analysis of bacterial community within different size particles was conducted by PCR-DGGE. The results indicated significant variation of bacterial community structure within different PSFs. The methane was predominantly produced in the coarser fractions, while more species and higher diversity of bacteria survived in the size of <2 μm fractions, in which the bacterial community structure was more significantly affected by fertilizer application practices than in the other coarser fractions. Higher bacterial species richness and more diversities in the smallest size fractions was due to the vicinity between microbes, access to carbon resource outside the microaggregates, and smaller pore size as protective agent suitable habitats for microbes rather than high SOC. Whereas, higher CO₂, CH₄ production and methanogenic archaeal community in coarser fractions may be contributed to storage of labile organic carbon in these fractions. It indicated that availability of SOC in PSFs is mainly factor affected survival of methanogenic archaeal community structure, whereas, bacterium community habitation more affected by physical protection of their location in PSFs. Their activity greatly depended on liability of SOC access to PSFs. Fertilizer application caused more change of bacteria community in clay fraction and greatly increased bacterium and methanogen activity in coarser fractions but only a slight effect on methanogenic archaeal community in the particle size fractions.     

Furanosyl Oxocarbenium Ion Conformational Energy Landscape Maps as a Tool to Study the Glycosylation Stereoselectivity of 2-Azidofuranoses, 2-Fluorofuranoses and Methyl Furanosyl Uronates

The 3D shape of glycosyl oxocarbenium ions determines their stability and reactivity and the stereochemical course of S_N1 reactions taking place on these reactive intermediates is dictated by the conformation of these species. The nature and configuration of functional groups on the carbohydrate ring affect the stability of glycosyl oxocarbenium ions and control the overall shape of the cations. We herein map the stereoelectronic substituent effects of the C2-azide, C2-fluoride and C4-carboxylic acid ester on the stability and reactivity of the complete suite of diastereoisomeric furanoses by using a combined computational and experimental approach. Surprisingly, all furanosyl donors studied react in a highly stereoselective manner to provide the 1,2-cis products, except for the reactions in the xylose series. The 1,2-cis selectivity for the ribo-, arabino- and lyxo-configured furanosides can be traced back to the lowest-energy ³E or E₃ conformers of the intermediate oxocarbenium ions. The lack of selectivity for the xylosyl donors is related to the occurrence of oxocarbenium ions adopting other conformations.     

Umweltchemie 1998

Nachdem im Trendbericht des letzten Jahres ausgewählte Beispiele aus Bereichen der Umweltchemie besprochen wurden,¹⁾ sollen in diesem Jahr Ergebnisse aus Ökotoxikologie and Humantoxikologie behandelt werden. Zunächst werden einige Arbeiten aus den Bereichen der Entsorgungsverfahren und neue Entwicklungen bei Spurenstoffen vorgestellt. Da das Gebiet der nachhaltigen Chemie immer mehr in den Brennpunkt des Interesses rückt, werden auch neue umweltfreundliche Synthesen und Produkte ausführlich diskutiert.