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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Macromolecules 27 (1994), S. 838-843 
    ISSN: 1520-5835
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 46 (1990), S. 2318-2320 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 47 (1991), S. 864-866 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 4
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 30 (1974), S. 616-625 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Lonsdale and Krishnan used a method for relating crystal and molecular susceptibilities in which they calculated the molecular tensor from the principal crystal susceptibilities assuming that the directions of the principal axes of the molecular tensor are known. Their method is only applicable when the molecular symmetry permits. To avoid this inconvenience and to allow an interpretation of molecular anisotropies in terms of chemical groups, we assume that each molecule consists of a skeleton on which different substitutions are made. The molecular tensor is thus the sum of the different elementary tensors associated with the molecule and related to an orthogonal and common set of axes. Several molecules with common skeletons and substitutions were studied to obtain the different elementary tensors; the set of equations which relate elementary tensor components to crystal susceptibilities in the approximation of weak intermolecular interactions was solved by a least-squares method. Our method was applied to benzene, hexachlorobenzene and hexamethylbenzene separately at first and then all together. The results are given for the substitution of a hydrogen atom by a chlorine atom or a methyl on a benzene ring. Several possible applications of this method are discussed.
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  • 5
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 30 (1974), S. 721-726 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The molecular diamagnetic susceptibilities of various benzenic compounds with C-CI, C-Br and C-NO2 groups have been determined using a method previously described. In order to interpret the molecular anisotropies in terms of chemical groups, it is assumed that each molecule consists of a benzenic skeleton on which different substitutions are made, and the set of equations is solved by a least-squares method. The contribution of the variation of the π-electron ring current has to be taken into account for a complete interpretation of the molecular susceptibilities. This contribution and the elementary tensors are then determined. Several possible applications of the method of molecular susceptibilities are illustrated and discussed.
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  • 6
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 30 (1997), S. 1075-1083 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Model liquid-crystalline ionomers have been synthesized, which consist of low molecular weight (700–49 000) linear ω- and α,ω-sodium sulfonato- and carboxylato-poly(styrenes or isoprenes) selectively end-capped at one or both end(s) with an ionic mesogenic group. These compounds are referred to as liquid-crystalline halato(semi)telechelic polymers [LC H(S)TPs]. A combination of small-angle X-ray scattering and small-angle neutron scattering studies on these LC H(S)TPs clearly shows the usual ionic peak related to interparticle interference between the ionic aggregates and a peak which can be related to the organization of a smectic mesophase. This mesogenic peak is generally masked by the foot of the broad ionic peak. The ionic peak Bragg spacing is much larger in the LC H(S)TP than in the H(S)TP precursor. This increased interaggregate distance results from the hindrance due to the mesogenic organization and from the restricted mobility experienced by the chains closely attached to the mesogen layers. As a rule, the lower the glass transition temperature of the polymeric matrix, the better the definition of the ionic peak. The ionic peak is well defined as long as the temperature is lower than the temperature of transition from solid to smectic phase (323 K). At higher temperatures, the ionic peak intensity decreases with increasing temperature.
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  • 7
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Applied crystallography online 30 (1997), S. 1065-1074 
    ISSN: 1600-5767
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Geosciences , Physics
    Notes: Various mesoporous silicas and the corresponding aluminosilicates or gallosilicates have been synthesized using a series of literature or `home made' recipes. The efficiency of Al or Ga incorporation in the siliceous walls of these materials depends markedly on the trivalent source and the evolution (ageing) of the so-formed Si-MIII gel-type phases at different starting pH values and temperatures, after adding the surfactant-structuring compounds. Crystallization at low temperature (e.g. 〈 373 K) yielded mesoporous compounds with hexagonal topology (MCM-41 type), involving double-layered Si walls possibly partly substituted by Al or Ga. Such structures remain stable after calcination in air at 873 K. When the same gels are crystallized at 423 K for 2 d, lamellar frameworks (MCM-50 type) are preferentially stabilized. They readily collapse on heating. The ultra-small-angle X-ray scattering (USAXS) data and the first part of the SAXS data show a power behaviour that indicates a fractal interface before calcination. After calcination, in the case of MCM-50 type materials, the fractal dimension significantly increases, the fractality region being larger than in the precursor. By contrast, in the case of MCM-41 type materials, the fractal region tends to disappear after calcination. The second part of the SAXS curve reflects the hexagonal or lamellar structure. Some precursors simultaneously exhibit both structures. The hexagonal parameter ranges from 4.6 to 5.8 nm, while the thickness of the wall is estimated to be of the order of 0.7 nm from observations of the satellite peaks in the vicinity of the successive peaks characterizing the hexagonal array. The successive peaks relative to the lamellar structure are consistent with the superposition of two or three layers, the thickness of which are of the order of 3.3, 2.85 and 2.5 nm. Predominant hexagonal structures are maintained after calcination while lamellar structures collapse during calcination. In the case of hexagonal structure, the hexagonal array is slightly contracted.
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  • 8
    Electronic Resource
    Electronic Resource
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 35 (1979), S. 203-205 
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
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  • 9
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 31 (1975), S. 318-322 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Within the framework of the research undertaken in the authors' laboratory, the magnetic anisotropy of some corticosteroids C21 has been studied. The diamagnetic molecular tensors are deduced from the measured crystal tensors by an original method. The orientation of the principal molecular axes with regard to the steroid skeleton is given.
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  • 10
    Electronic Resource
    Electronic Resource
    [S.l.] : International Union of Crystallography (IUCr)
    Acta crystallographica 31 (1975), S. 609-611 
    ISSN: 1600-5724
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The molecular refractivities of some corticosteroids C21 are calculated from the crystal refractivities. The latter are obtained from the measured principal refractive indices. The orientations of the principal molecular axes with regard to the steroid skeleton are given and the magnetic and optical anisotropies compared.
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