Kozlova Marina N, Ferlay Sylvie, Solovieva Svetlana E, Antipin Igor S, Konovalov Alexander I, Kyritsakas Nathalie, Hosseini Mir Wais
Laboratoire de Chimie de Coordination Organique, UMR CNRS 7140, Université Louis Pasteur, Institut Le Bel, 4 rue Blaise Pascal, F-67000 Strasbourg, France.
Dalton Trans. 2007 Nov 28(44):5126-31. doi: 10.1039/b712351e. Epub 2007 Sep 20.
Two new p-tert-butylthiacalix[4]arene derivatives 2 and 3 decorated at the lower rim with four nitrile groups have been prepared and structurally characterised in the crystalline phase. The two ligands, differing by the length of the spacer between the calix moiety and the nitrile group, adopt the 1,3-alternate conformation in the solid state. The ligand 3 bearing four (CH(2))(3)CN fragments behaves as a tecton in the presence of silver salts (AgX, X = BF(4), PF(6) or SbF(6)) and leads to the formation of analogous 1-D linear coordination networks. The tecton 3 acts as a bischelate unit and bridges consecutive silver cations adopting a tetrahedral coordination geometry. Anions and solvent molecules occupy the free space between networks and exhibit no specific interactions with the cationic architecture.
已经制备了两种在下边缘带有四个腈基的新型对叔丁基硫杂杯[4]芳烃衍生物2和3,并对其晶相结构进行了表征。这两种配体在杯芳烃部分和腈基之间的间隔长度不同,在固态下采用1,3-交替构象。带有四个(CH(2))(3)CN片段的配体3在银盐(AgX, X = BF(4)、PF(6)或SbF(6))存在下表现为构造体,并导致形成类似的一维线性配位网络。构造体3作为双螯合单元,桥连连续的银阳离子,采用四面体配位几何结构。阴离子和溶剂分子占据网络之间的自由空间,并且与阳离子结构没有特定的相互作用。