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  • Chemistry  (50)
  • Analytical Chemistry and Spectroscopy  (6)
  • Humans
  • Surface physics, nanoscale physics, low-dimensional systems
  • 1995-1999  (24)
  • 1990-1994  (27)
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  • 1
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part A: Polymer Chemistry 28 (1990), S. 2249-2254 
    ISSN: 0887-624X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The aqueous polymerization of methyl metacrylate in the presence of thiourea and hydrogen montmorillonite was initiated by radicals generated in situ. A part of the polymer was bound to the clay. Electrochemical analysis by cyclic voltammetry on this system and FeCl3/thiourea indicated that a slow one-electron transfer process was responsible for the formation of the amidosulfenyl radical. The oxidant in the clay was lattice substituted Fe3+.
    Additional Material: 2 Ill.
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  • 3
    ISSN: 0899-0042
    Keywords: diols ; hydroperoxides ; absolute configuration ; exciton coupling ; circular dichroism ; enantiomeric separation ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Allylic hydroperoxides are a class of compounds of versatile synthetic utility. Optically active diastereomeric hydroperoxy homoallylic alcohols and their corresponding diols are easily available through horseradish peroxidase (HRP)-catalyzed kinetic resolution of racemic hydroperoxides. Here we describe the assignment of the absolute configuration of the optically active products and substrates obtained after HRP-catalysis by the circular dichroism exciton chirality method. Moreover, the analytical-scale separation of the enantiomers based on multidimensional gas chromatography on chiral columns is presented. Since the enantiomeric elution order on the ciral columns was constituted, the absolute stereochemistry of optically active allylic diols can easily be deduced by their retention times on β-cyclodextrins. Chirality 9:69-74, 1997. © 1997 Wiley-Liss, Inc.
    Additional Material: 5 Ill.
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  • 4
    ISSN: 1434-193X
    Keywords: Lipase ; 2-Hydroxy acids ; Kinetic resolution ; Acetylation ; Biocatalysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The lipase-catalyzed acetylation of a broad spectrum of racemic 2-hydroxy acids 1 to their 2-acetoxy acids 2 was shown to proceed with high enantioselectivity. Thus, the microbial lipases, in particular from Candidaantarctica and Burkholderiaspecies, are convenient biocatalysts for the synthesis of optically active 2-hydroxy acids in excellent enantioselectivity (ee values up to 〉 99%). The absolute configurations of the 2-hydroxy acids 1 were assigned by comparison of the gas-chromatographic data with that of literature-known reference compounds, or by means of the exciton-coupled circular dichroism method (ECCD) on their bichromophoric 2-naphthoate 9-anthrylmethyl derivatives 3. These results establish that (S)-2-hydroxy acids 1 were preferentially acetylated by microbial lipases.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1998 (1998), S. 1585-1587 
    ISSN: 1434-1948
    Keywords: Metallodisilanes ; Oxofunctionalization ; Metallodisilandiols ; Silanetriols ; Metallosiloxanes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reaction of the ferriodisilanes C5R5(OC)2Fe-Si2H5 [R = H (1a), Me (1b)] with dimethyldioxirane leads to selective insertion of oxygen into the α-Si-H bonds to yield the ferriodihydroxydisilanes C5R5(OC)2Fe-Si(OH)2-SiH3[R = H (2a), Me (2b)]. Another access to yield 2a is opened by hydrolysis of the dichloro(ferrio)disilane Cp(OC)2Fe-SiCl2-SiH3 (3a). Treatment of the pentachloro(metallo)disilanes C5H5(OC)2Fe-Si2Cl5 (4a) and C5Me5(OC)2Ru-Si2Cl5 (4b) with water results in regiospecific hydroxylation of the β-silicon atom to generate metallodisilanetriols C5R5(OC)2M-SiCl2-Si(OH)3 [M = Fe, R = H (5a); M = Ru, R = Me (5b)]. Controlled condensation of 5b with Me2Si(H)Cl leads to the novel rutheniosiloxane C5Me5(OC)2Ru-SiCl2-Si(OSiMe2H)3 (6).
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 70 (1998), S. 909-917 
    ISSN: 0020-7608
    Keywords: charge transfer ; α-particles ; alkali atoms ; MO expansion ; close coupling ; Chemistry ; Theoretical, Physical and Computational Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cross sections for single-electron capture by α-particles from ground state K and Rb were calculated in the low-to-intermediate energy region by employing the molecular expansion method in the framework of impact parameter formulation. The colliding partners are treated as a pseudo-one-electron system and the technique of the pseudopotential is used to account for their mutual interactions. The molecular wave function of the quasimolecule formed during the collision is expanded in terms of basis sets of atomic orbitals on two centers. The resulting coupled equations are solved semiclassically where a straight-line trajectory describes the relative motion of the two nuclei. The effect of electron translation is also suitably incorporated. The calculated cross sections, both total and partial, are presented and compared with the available experimental measurements.   © 1998 John Wiley & Sons, Inc. Int J Quant Chem 70: 909-917, 1998
    Additional Material: 4 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Macromolecular Rapid Communications 18 (1997), S. 261-265 
    ISSN: 1022-1336
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: Polymerization of acrylamide with the redox couple Fe(III)/thiourea in the presence of the mineral clay montmorillonite has been investigated. Polyacrylamide is obtained in good yield having molecular weight (ca. 0.7-2.5 × 106) approximately one order of magnitude higher than without clay. Apparently, the locus of polymerization is the interlayer space of the clay.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Bognor Regis [u.a.] : Wiley-Blackwell
    Journal of Polymer Science Part B: Polymer Physics 30 (1992), S. 427-431 
    ISSN: 0887-6266
    Keywords: vinyl polymerization, redox initiated, ESR study of ; electron spin resonance (ESR) study of redox initiated vinyl polymerization ; radical mechanism of redox initiated vinyl polymerization ; Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Notes: An electron spin resonance (ESR) study confirms a free radical mechanism for aqueous vinyl polymerization initiated by three redox systems involving thiourea. The primary radical, NH2—C (=NH)S., could not be detected by ESR spectroscopy, perhaps because of its large g anisotropy and/or very short relaxation time. Propagating radicals are trapped from methyl-methacrylate by 2-methyl-2-nitroso propane (MNP) and their structures are found to be the same as those produced by either azo-bis-isobutyrnitrile or di-t-butyl peroxylate. The latter monomer, however, reacts with MNP in the absence of any initiator, giving different ESR lines.
    Additional Material: 3 Ill.
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 50 (1993), S. 555-556 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Additional Material: 3 Tab.
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Applied Polymer Science 60 (1996), S. 657-662 
    ISSN: 0021-8995
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics , Physics
    Notes: Unidirectional (UD) composite laminates based on glass fibers (GF) and high-performance polyethylene fibers (PEF) were prepared with partially polymerized methyl methacrylate (MMA) at room temperature and then heated at 55°C (well below the softening point of PEF) for 2 hrs. The viscoelastic behavior of the composite was studied through dynamic mechanical analysis at different volume fractions of fibers. Several parameters such as storage modulus (E′), loss modulus (E″), and loss factor or damping efficiency (tan ∂) were determined to be between 40 and 160°C in a resonant frequency mode. All the properties were compared between the two composite laminates. It was found that the shift of the glass transition temperature (Tg) due to incorporating fibers was higher in the case of a PEF-reinforced composite than that of a GF-reinforced composite at the same volume fraction of fibers. It was also observed that the efficiency of both the composites decreases with the increase in the volume fraction of fibers. © 1996 John Wiley & Sons, Inc.
    Additional Material: 6 Ill.
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