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  • Articles  (41)
  • 1985-1989  (23)
  • 1980-1984  (13)
  • 1970-1974  (5)
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  • 1
    Electronic Resource
    Electronic Resource
    The influence of spatial correlation of concrete strength on the failure probabilities of reinforced concrete chinneys (1989)
    Springer
    Materials and structures 22 (1989), S. 255-263 
    Details
    ISSN: 1359-5997
    Source: Springer Online Journal Archives 1860-2000
    Topics: Architecture, Civil Engineering, Surveying
    Notes: Abstract A procedure to estimate the failure probabilities of reinforced concrete (R/C) chimneys under severe wind loading which allows for considering realistic correlation values of concrete strength is developed. The results show that the assumption of full correlation of concrete strength within cross-sections, as suggested for example in present codes, may significantly overestimate the failure rates in present examples by two orders of magnitude. However, it is also shown that not only one but a number of cross-sections may contribute to the total failure rate of R/C chimneys. As a consequence, the failure estimates increase, in some cases by as much as two orders of magnitude. In the numerical examples as investigated here these counteracting effects neutralize each other. This fact, however, should not be generalized.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF02472557
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  • 2
    Electronic Resource
    Electronic Resource
    Neue Lanthanoidmagnetoplumbite: LaFe11A1019, SmFe4Al8O19 und Eu0,83Fe2Al10O19 (1982)
    Springer
    Monatshefte für Chemie 113 (1982), S. 1079-1085 
    Details
    ISSN: 1434-4475
    Keywords: Aluminium ; Crystal Structure ; Iron ; Oxygen ; Rare Earth
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract New compounds of magnetoplumbite structure with rare earth-ions were prepared by solid state reactions and determined by X-ray single crystal work. They crystallize in space group D 6h 4 -P63/mmc withA:a=582.6,c=2283;B:a=563.4,c=2208;C:a=565.8,c=2218 pm. The distribution of Fe and Al to the metal positions were determined and the thermal ellipsoids of the metal positions are discussed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00808621
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  • 3
    Electronic Resource
    Electronic Resource
    Generation of the Gaussian-like HE11 mode from gyrotron TEOn mode mixtures at 70 GHz (1985)
    Springer
    International journal of infrared and millimeter waves 6 (1985), S. 459-470 
    Details
    ISSN: 1572-9559
    Keywords: high-power millimeter waves ; gyrotron ; electron cyclotron resonance heating (ECRH) ; overmoded waveguide systems ; mode conversion ; linearly polarized narrow pencil beam
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract This work reports calculations and measurements on mode converters for the transformation of TEOn gyrotron mode mixtures (primarily TEO2) into the linearly polarized HE11 hybrid mode at 70 GHz. This mode is ideal for quasi-optical launching systems for ECRH of plasmas. Mode transducers with axisymmetric radius perturbations convert the gyrotron TEOn mode composition into the TEO1 mode. Proper matching of the phase differences between the various modes and of the perturbation amplitudes of the several converter sections is required. The TEO1 wave is used for long-distance transmission through smooth-walled overmoded waveguides. A mode converter with constant diameter and periodically perturbed curvature transfers the unpolarized TEO1 mode into the polarized TE11 wave. The experimentally determined ΣTEOn-to-TEO1 conversion efficiency is (98.5±1)% (99% predicted) while the TEO1-to-TE11 transformer has a (94±2)% efficiency (93% theoretically); ohmic losses are included. The “Gaussian-like” HE11 mode with axisymmetric power distribution and almost no cross polarization is produced in a circumferentially corrugated TE11-to-HE11 mode transducer with a measured conversion efficiency of (98.3±1.5)% (98.5% predicted). The overall efficiency of the complete mode converter system in the desired mode was determined to be (91±2.5)%. High-power operation (200kW, 100ms) has been successfully demonstrated.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF01010037
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  • 4
    Electronic Resource
    Electronic Resource
    The fluidity of plasma membranes from ethanol-treated rat liver (1984)
    Springer
    Molecular and cellular biochemistry 64 (1984), S. 89-95 
    Details
    ISSN: 1573-4919
    Keywords: ethanol ; plasma membranes ; phospholipid (rat liver) ; miocroviscosity
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology , Medicine
    Notes: Summary Male Wistar rats were maintained for 35–40 days on a liquid diet containing 36% of calories as ethanol. Ethanol was replaced by carbohydrates in the isocaloric diet fed to control animals. The effect of ethanol consumption has been studied on the fluorescence polarization of rat liver plasma membranes and artificial lipid vesicles and on the lipid composition of the membranes. Fluorescence polarization in both membranes and vesicles was determined using DPH and TMA-DPH as fluorescence markers; from these data, the polarization term (ro/r−1)−1 and flow activation energy (ΔE) were calculated. The ethanol consumption induces a more fluid environment within the membrane core of liver plasma membranes; the ethanol-fed rat membranes are more resistant to the in vitro effect of ethanol disordering the membrane structure. Vesicles obtained with lipids from either control membranes or ethanol-fed rat membranes were treated with ethanol and the changes in polarization paralleled to those exhibited by the membranes. The absence of phase transitions and of ΔE changes was also shown in temperature-dependence studies. The lower cholesterol content found in ethanol-fed rat plasma membranes might be responsible for observed variations in the microviscosity.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00420932
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  • 5
    Electronic Resource
    Electronic Resource
    Putative target sites for mobile G+C rich clusters in yeast mitochondrial DNA: Single elements and tandem arrays (1989)
    Springer
    Molecular genetics and genomics 218 (1989), S. 272-283 
    Details
    ISSN: 1617-4623
    Keywords: GC clusters ; Mobile elements ; Target sites ; mtDNA ; Saccharomyces cerevisiae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary GC clusters constitute the major repetitive elements in the mitochondrial (mt) genome of the yeast Saccharomyces cerevisiae. Many of these clusters are optional and thus contribute much to the polymorphism of yeast mtDNAs. We have made a systematic search for polymorphic sites by comparing mtDNA sequences of various yeast strains. Most of the 26 di- or polymorphic sites found differ by the presence or absence of a GC cluster of the majority class, here referred to as the M class, which terminate with an AGGAG motif. Comparison of sequences with and without the GC clusters reveal that elements of the subclasses M1 and M2 are inserted 3′ to a TAG, flanked by A+T rich sequences. M3 elements, in contrast, only occur in tandem arrays of two to four GC clusters; they are consistently inserted 3′ to the AGGAG terminal sequence of a preexisting cluster. The TAG or the terminal AGGAG, therefore, are regarded as being part of the target sites for M1 and M2 or M3 elements, respectively. The dinucleotide AG is in common to both target sites; it also occurs at the 3′ terminus (AGGAG). This suggests its duplication during GC cluster insertion. This notion is supported by the observation that GC clusters of the minor classes G and V similarily repeat at their 3′ terminus a GT or an AA dinucleotide, respectively, from their putative target sites.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00331278
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  • 6
    Electronic Resource
    Electronic Resource
    Isolation and expression analysis of two yeast regulatory genes involved in the derepression of glucose-repressible enzymes (1987)
    Springer
    Molecular genetics and genomics 209 (1987), S. 366-373 
    Details
    ISSN: 1617-4623
    Keywords: Glucose repression ; Glucose derepression ; Regulatory genes ; Expression analysis ; Saccharomyces cerevisiae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Yeast strains carrying one of the two regulatory mutations cat1 and cat3 are defectve in derepression of several glucose-repressible enzymes that are necessary for utilizing non-fermentable carbon sources. Hence, these strains fail to grow on ethanol, glycerol or acetate. The synthesis of isocitrate lyase, malate synthase, malate dehydrogenase and fructose-1,6-bisphosphatase is strongly affected in cat1 and cat3 strains. Genes CAT1 and CAT3 have been isolated by complementation of the cognate, mutations after transformation with an episomal plasmid gene library. The restriction map of CAT1 proved its allelism to the earlier isolated SNF1 gene. Both genes appear to exist as single-copy genes per haploid genome as indicated by Southern hybridization. Northern analysis has shown that the 1.35 kb CAT3 mRNA is constitutively expressed, independent of the carbon source in the medium. Derepression studies with CAT3 transformants using a multi-copy plasmid showed over-expression of glyoxylate cycle enzymes. This result would be consistent with a direct effector function for the CAT3 gene product.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00329667
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  • 7
    Electronic Resource
    Electronic Resource
    Verzweigte und kettenverlängerte Zucker, XXX. Diastereoselektive Synthese von L-glycero-D-manno-Heptose, einem Baustein der inneren Core-Region von Lipopolysacchariden (1986)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1986 (1986), S. 675-686 
    Details
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Branched and Chain-extended Sugars, XXX.  -  Diastereoselective Synthesis of L-glycero-D-manno-Heptose, a Constituent of the Inner Core Region of LipopolysaccharidesReaction of 2,3;5,6-di-O-isopropylidene-D-mannofuranose (1) with 2-lithio-1,3-dithiane affords diastereoselectively the 3,4;6,7-di-O-isopropylidene-D-glycero-D-galacto-heptose trimethylene dithioacetal (3). Conversion of compound 3 by a sequence of steps gives the tri-O-isopropylidene-D-glycero-D-galacto-heptit 16 which is oxidized with 1,1′-(azodicarbonyl)-dipiperidine to give the tri-O-isopropylidene-L-glycero-D-manno-heptose 17. Finally, compound 17 is transferred via the acetate 19 into the L-glycero-D-manno-heptopyranose 18.
    Notes: 2,3;5,6-Di-O-isopropyliden-D-mannofuranose (1) reagiert diastereoselektiv mit 2-Lithio-1,3-dithian zum 3,4;6,7-Di-O-isopropyliden-D-glycero-D-galacto-heptose-trimethylendithioacetal (3). Nach Umwandlung von 3 über eine Reihe von Zwischenstufen zum Tri-O-isopropyliden-D-glycero-D-galacto-heptit 16 läßt sich dieser mit 1,1′-(Azodicarbonyl)dipiperidin zur Tri-O-isopropyliden-L-glycero-D-manno-heptose 17 oxidieren. Hieraus ist über das Acetat 19 die freie L-glycero-D-manno-heptopyranose 18 zu gewinnen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.198619860409
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  • 8
    Electronic Resource
    Electronic Resource
    Bausteine von Oligosacchariden, LXXVIII. Synthese von KDO-haltigen Lipoid-A-Analoga (1987)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1987 (1987), S. 249-258 
    Details
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Building Units of Oligosaccharides, LXXVIII. - Synthesis of KDO-Containing Lipid A AnaloguesThe non-neighbouring group supported glycosidation of 12 with the suitably protected glycosyl bromide 9 of 2-azido-2-deoxy-D-glucose leads - in the presence of a heterogeneous silver catalyst - to the formation of the β-(1→6)-glycosidically linked disaccharide 14. It consists of two 2-azido-2-deoxy-D-glucose units. Partial deblocking of 14 furnishes 15. On glycosidation with KDO bromide this compound yields the trisaccharide 16, which contains a KDO unit in an α-(2→6) ketosidic bond. Reduction of the two azido groups followed by amidation with (R)-3-hydroxymyristic acid and further deblocking generates the trisaccharide α-KDO-(2→6)-β-D-GlcA-(1→6)-D-GlcA 20 with two 3-hydroxy fatty acid residues in an amidic linkage.
    Notes: Die Umsetzung des Pyranosylbromids 9 der 2-Azido-2-desoxy-D-glucose mit dem Akzeptor 12 führt bei Gegenwart eines heterogenen Silberkatalysators ohne Nachbargruppenbeteiligung unter Inversion zum β-(1→6)-glycosidisch verknüpften Disaccharid 14 aus zwei 2-Azido-2-desoxy-D-glucose-Einheiten. Nach partieller Entblockierung zu 15 ist die Anknüpfung eines KDO-Restes unter Bildung einer α-(2→6)-ketosidischen Bindung zum Trisaccharid 16 möglich. Nach Reduktion der Azidogruppen und Anknüpfung von (R)-3-Hydroxymyristinsäure-Resten gelangt man nach Entblockierung zum Trisaccharid α-KDO-(2→6)-β-D-GlcA-(1→6)-D-GlcA 20, das amidartig zwei 3-Hydroxyfettsäure-Reste gebunden enthält.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.198719870316
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  • 9
    Electronic Resource
    Electronic Resource
    Die Massenspektren der Nikotin-N-Oxide und der mit Ihnen Verwandten Tetrahydrooxazine (1973)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 7 (1973), S. 839-843 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The mass spectra of the three nicotine-N-oxides are discussed, together with the spectra of tetrahydrooxazines. The compounds with an N-oxide function in the five membered ring partly rearrange thermally before electron-impact fragmentation.
    Notes: Die massenspektren der drei Nikotin-N-oxide werden zusammen mit den Spektren von Tetrahydrooxazinen diskutiert. Die Verbindungen mit N-Oxide-Ffunktion im 5-gliedrigen Ring lagern sich vor der Fragmentierung durch Elektronenstoß z.T. thermisch um.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210070708
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  • 10
    Electronic Resource
    Electronic Resource
    Struktureller Zusammenhang von [(C6H5)4As]NdCl4·8H2O und NdCl3·6H2O: übergang vom Raumnetz zur Schicht (1983)
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 95 (1983), S. 1031-1032 
    Details
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ange.19830951239
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