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  • 2010-2014  (91)
  • 2000-2004  (57)
  • 1975-1979  (20)
  • 1960-1964
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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 79 (1975), S. 2531-2535 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Woodbury, NY : American Institute of Physics (AIP)
    Applied Physics Letters 79 (2001), S. 1118-1120 
    ISSN: 1077-3118
    Source: AIP Digital Archive
    Topics: Physics
    Notes: We report a reduction of inhomogeneous broadening in CdSe-related quantum wells in ZnSe by employing a growth technique that uses a CdS-compound source instead of the standard Cd elemental source for molecular-beam epitaxy. Assisted by the low sticking coefficient of sulfur and possibly an exchange reaction between S and Se, only a small S contamination is observed. A comparison with standard layers reveals an increase in quality and homogeneity by a strong reduction of the photoluminescence (PL) linewidth. Samples obtained by our method show extremely little lateral confinement as indicated by a lack of sharp single dot emission lines in micro PL and the absence of the extensive redshift observed in temperature dependent PL of fluctuating well potentials. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 1170-1177 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We measured absolute partial cross sections for the formation of various singly charged and doubly charged positive ions produced by electron impact on SiF4 from threshold to 900 eV using a time-of-flight mass spectrometer. Dissociative ionization was found to be the dominant process, although we found evidence of the presence of the SiF4+ parent ion in our experiment. The SiF3+ fragment ion has the largest partial ionization cross section with a maximum value of 4.3×10−16 cm2 at 90 eV. All other singly charged fragment ion cross sections are about one order of magnitude smaller at this impact energy. The cross-section values of the doubly charged ions with the exception of SiF2++ are about two orders of magnitude smaller. A comparison is made with available previously measured data. Additional measurements using a sector-field mass spectrometer revealed that all fragment ions are formed with excess kinetic energy. The experimentally determined total single ionization cross section of SiF4 is compared with results of semiempirical and semiclassical calculations and reasonable agreement is found. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Science, Ltd
    Molecular microbiology 40 (2001), S. 0 
    ISSN: 1365-2958
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology , Medicine
    Notes: The diffuse adherence of Escherichia coli strain 2787 (O126:H27) is mediated by the autotransporter adhesin AIDA-I (adhesin-involved-in-diffuse-adherence) encoded by the plasmid-borne aidA gene. AIDA-I exhibits an aberrant mobility in denaturing gel electrophoresis. Deletion of the open reading frame (ORF) A immediately upstream of aidA restores the predicted mobility of AIDA-I, but the adhesin is no longer functional. This indicates that the mature AIDA-I adhesin is post-translationally modified and the modification is essential for adherence function. Labelling with digoxigenin hydrazide shows AIDA-I to be glycosylated. Using carbohydrate composition analysis, AIDA-I contains exclusively heptose residues (ratio heptose:AIDA-I ≈19:1). The deduced amino acid sequence of the cytoplasmic open reading frame (ORF) A gene product shows homologies to heptosyltransferases. In addition, the modification was completely abolished in an ADP–glycero-manno-heptopyranose mutant. Our results provide direct evidence for glycosylation of the AIDA-I adhesin by heptoses with the ORF A gene product as a specific (mono)heptosyltransferase generating the functional mature AIDA-I adhesin. Consequently, the ORF A gene has been denoted ‘aah’ (autotransporter-adhesin-heptosyltransferase). Glycosylation by heptoses represents a novel protein modification in eubacteria.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1434-6036
    Keywords: PACS. 74.72.Jt Other cuprates – 79.60.-i Photoemission and photoelectron spectra – 74.25.Jb Electronic structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Physics
    Notes: Abstract: In recent years insight has been gained into the electronic structure of layered cuprates using angle-resolved photoelectron spectroscopy. In many of these studies it is assumed that the electron-photon matrix element follows the trends set by the atomic photoionization cross sections and does not influence lineshape, dispersion and the k-dependence of the spectral intensity. In this study using Sr2CuO2Cl2 as an example it will be shown that the electron-photon matrix element can have a strong impact on both strength and shape of a feature in an angle-resolved photoelectron spectrum of a layered cuprate which can strongly affect information on character and the momentum-dependence of the energy and spectral weight of a state deduced from the spectra. The results of this study put an emphasis on the need to employ the whole parameter range of the ARPES method to get reliable information on the spectral function of cuprates for which purpose synchrotron radiation is an uniquely suited tool.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. ; Stafa-Zurich, Switzerland
    Key engineering materials Vol. 206-213 (Dec. 2001), p. 219-222 
    ISSN: 1013-9826
    Source: Scientific.Net: Materials Science & Technology / Trans Tech Publications Archiv 1984-2008
    Topics: Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
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  • 7
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Characterization of Weak Bonded Solid 1:1 Adducts Formed between Antimony(III) Halogenides and s-TrithianeCrystalline 1:1 addition compounds are formed on cooling hot solutions of antimony(III) halides and s-trithiane in benzene or toluene. Their preparation, physical properties and vibrational spectra are described.
    Notes: Aus den Gemischen heißer Lösungen von s-Trithian und Antimon(III)-Halogeniden in Benzol oder Toluol kristallisieren beim Erkalten 1:1-Additionsverbindungen. Ihre Darstellung, physikalischen Eigenschaften und Schwingungsspektren werden beschrieben.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 418 (1975), S. 208-216 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Some Substitution Reactions of Trimeric ThioformaldehydeTreatment of s-trithiane with n-butyllithium results in the formation of lithium salts of carbenium ions. Their reactions with the halo-functional compounds lead to mono- or multi-substituted trithianes besides lithium chloride.
    Notes: Die Behandlung von s-Trithian mit n-Butyllithium führt zu Lithiumsalzen von Carbanionen. Bei der Umsetzung mit den halogenfunktionellen Verbindungen CH3J. (CH3)3SiCl, (CH3)3GeCl, (CH3)3SnCl und (CH3)2SiCl2 reagieren diese unter Abspaltung von LiCl zu ein- oder mehrfach substituierten s-Trithianen.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 437 (1977), S. 159-161 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Isomerizations of Triple Substituted s-TrithianeTreatment of triple silyl-substituted s-trithiane with n-butyllithium results in the formation of lithium salts of carbenium ions. Their reactions with water or heavy water lead to isomers of 2,4,6-tris-(trimethylsilyl)-s-trithianes.
    Notes: Dreifach silyliertes s-Trithian wird mit überschüssigem n-Butyllithium umgesetzt. Die entstehenden Lithiumsalze von Carbanionen ergeben bei Zusatz von Wasser bzw. Deuteriumoxid Isomere des 2,4,6-Tris-(trimethylsilyl)-s-trithians.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Carbonyl Metal Compounds with Polydentate Cyclic Ligands. I. Pentacarbonyl Complexes of s-Trithiane and Related CompoundsThe complexes (RCHS)nM(CO)5 (R = H, CH3, n = 3; R = H, n = 4; M = Cr, Mo, W) were prepared from the tetrahydrofuran pentacarbonyl metal compounds and the respective ligands. The Cotton-Kraihanzel force constants of these complexes indicate the sulfur ligands to be slightly more basic than triphenylphosphine. The trimethyltrithiane complexes (R = CH3, n = 3) exhibit rapid intramolecular exchange of the M(CO)5-group along the three coordination centers of the ligand.
    Notes: Die Komplexe (RCHS)nM(CO)5 (R = H, CH3, n = 3; R = H, n = 4; M = Cr, Mo, W) wurden aus den Tetrahydrofuran-pentacarbonylmetallverbindungen und dem jeweiligen Liganden dargestellt. Die Cotton-Kraihanzel-Kraftkonstanten dieser Komplexe weisen die Schwefelliganden als geringfügig schwächere Akzeptoren, verglichen mit Triphenyl-phosphin, aus. Die Komplexe des Trimethyltrithians (R = CH3, n = 3) zeigen einen raschen intramolekularen Austausch der M(CO)5-Gruppe über die drei Koordinationsstellen des Liganden.
    Additional Material: 4 Tab.
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