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  • 1
    ISSN: 1573-1111
    Keywords: Crystal structure ; clathrate ; 4-methylpyridine ; Cu(II) ; Mn(II)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The crystal structures of the two clathrates with the composition [M(4-MePy)4(NCS)2]·0.67(4-McPy)·0.33 H2O (M=Cu(II), Mn(II); 4-MePy=4-methylpyridine) have been determined. These compounds are trigonal, with the [M(4-MePy)4(NCS)2] host molecules being centrosymmetric. The parameters of the unit cells area = 27.365(7) and 27.738(6),c = 11.303(9) and 11.250(8) Å,V = 7325(2) and 7493(2) Å3, space group R $$\bar 3$$ , R = 0.053 and 0.109 for M = Cu(II) and Mn(II), respectively. ForZ = 9d calcd is equal to 1.271 and 1.225 g/cm3, andd measd is equal to 1.252(2) and 1.213(2) g/cm3 for the Cu and Mn clathrates, respectively. The coordination environment of the metal atoms in these compounds is an irregular octahedron, while in the Mn compound these distortions are rather small (Mn-NMePy 2.30, 2.34 Å, Mn-NNCS 2.18 Å, and Cu-NMePy 2.06 Å, Cu-NNCS 1.98 Å and Cu-NMePy 2.50 Å). The molecular packing in the structures is such that the channels of variable diameter are formed along the short cell dimension (the maximum diameter is ≅ 10 Å, the minimum being ≅ 6 Å) where the guest 4-MePy and H2O molecules are placed.
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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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