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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 18 (1994), S. 317-329 
    ISSN: 1573-1111
    Keywords: Crystal structure ; clathrate ; Werner complex ; isothiocyanate ; 4-methylpyridine ; Mg(II)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Two clathrate modifications of the title host with 4-methylpyridine (4-CH3C5H4N) as a guest have been determined at −50°C. [Mg(4-CH3C5H4N)4(NCS)2] · 2/3(4-CH3C5H4N) · 1/3H2O is trigonal, space group $$R\bar 3$$ , witha=27.630(7),c=11.219(3) ÅV=7417(4) Å3,Z=9,D calc=1.171 g cm−3,μ(CuK α)=18.506 cm−1, finalR=0.064. [Mg(4-CH3C5H4N)4(NCS)2] · (4-CH3C5H4N) is tetragonal, space group I4l/a, witha=16.944(7),c=23.552(9)Å,V=6762(5) Å,Z=8,D calc=1.191 g cm−3, μ(CuK α)=18.200 cm−1, finalR=0.071. The structures consist of molecular packings of the same host complex units and the guest species. The Mg(II) cation is octahedrally coordinated to theN-atoms of four 4-methylpyridine and twotrans-coordinated isothiocyanato ligands in the host molecule. The conformations of the molecule are considerably different both in symmetry and in geometry in these two structures. The guest 4-methylpyridine molecules are disordered into channels which have different topology in these two clathrates resulting in different thermal stability.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of inclusion phenomena and macrocyclic chemistry 17 (1994), S. 305-316 
    ISSN: 1573-1111
    Keywords: Phase diagram ; clathrate ; X-ray structure ; 4-methylpyridine ; Zn(II) isothiocyanate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A phase diagram of the [Zn(MePy)2(NCS)2]-MePy binary system has been studied by DTA and solubility methods. Two compounds melting incongruently (at 63 and 57°C) have been discovered in the system. They have been obtained as separate phases with crystals of different shape (needles and octahedra). Their composition has been determined by analytical methods and verified by X-ray structural analysis: [Zn(MePy)4(NCS)2]·0.67 MePy·xH2O, wherex depends on the synthesis conditions, and [Zn(MePy)4(NCS)2]·MePy, respectively. The preliminary X-ray study of the first compound (at −100°C) has shown it to be isostructural with the known clathrates of the common formula [M(MePy)4(NCS)2]·0.67MePy·xH2O, where M=Cu, Mn, Mg andx=0–0.33. The unit cell parameters are as follows:a=27.20(1),c=11.202(4) Å, space group $$R\bar 3$$ ,Z=9. The X-ray study of [Zn(MePy)4(NCS)2]·MePy (at−50°C) has shown it to be analogous to the ‘organic zeolite’ β-phase with the guest MePy molecules located in the channels formed by molecular packing of the [Zn(MePy)4(NCS)2]host. The cell is tetragonal, the space groupI41/a,a=16.845(6),c=23.496(7) Å,V=6667(4) Å3,Z=8,D calc=1.289 g cm−3,R=0.074. The zinc cation is surrounded by a slightly irregular octahedron of six nitrogen atoms of the MePy and NCS ligands. The crystallisation field of the host [Zn(MePy)4(NCS)2] complex in the temperature range concerned is absent in the phase diagram. It suggests contact stabilization of the [Zn(MePy)4(NCS)2] molecule by the guest in the clathrates.
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