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Supramolecular Recognition: Use of Cofacially Disposed Bis-terpyridyl Square-Planar Complexes in Self-Assembly and Molecular Recognition

机译:超分子识别:在自组装和分子识别中使用表面处理的双萜基双平面配合物。

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摘要

A molecular receptor consisting of a molecular spacer that constrains two terpyridyl-palladium(II) complexes to be disposed in a parallel cofacial geometry has been prepared. The separation between the two terpyridyl-palladium units is enforced to be ca. 7 A, a distance sufficient to incarcerate aromatic molecules and square-planar complexes. A number of molecules are shown to associate with this spacer-chelator complex. In particular, 9-methylananthracene (9-MA) is found to form a 1:2 host-guest complex. A crystal structure of this complex shows one 9-MA in the molecular cleft formed by the two terpyridyl-palladium units and the other 9-MA molecule to lie above one of the terpyridyl-palladium units. Nuclear Overhauser effects on analogous molecules that contain two anthracene guests tethered intramolecularly indicate that the structure found in the solid is similar to that in solution. Low-temperature ~1H-NMR studies indicate rapid exchange between the two binding sites. The spacer-chelator complexes, when combined with appropriate molecular linders, readily form molecular rectangles, trigonal prismas, and tetragonal prisms. One molecular rectangle is shown to associate with up to five 9-MA molecules.
机译:制备了由分子间隔基组成的分子受体,该分子间隔基限制了两个以平行的界面几何形状排列的叔丁基-钯(II)配合物。两个叔吡啶基-钯单元之间的间隔被强制为约。在图7A中,该距离足以嵌顿芳族分子和方形平面络合物。示出了许多分子与此间隔-螯合剂复合物缔合。特别地,发现9-甲基蒽蒽(9-MA)形成1:2的宿主-客体复合物。该络合物的晶体结构显示在由两个吡啶基-钯单元形成的分子裂缝中的一个9-MA,而另一个9-MA分子位于一个吡啶基-钯单元之上。核Overhauser效应对包含两个分子内束缚的蒽客体的类似分子的影响表明,固体中发现的结构类似于溶液中的结构。低温〜1H-NMR研究表明两个结合位点之间快速交换。间隔-螯合剂配合物,当与适当的分子衬垫结合时,容易形成分子矩形,三棱柱和四棱柱。示出一个分子矩形与多达五个9-MA分子缔合。

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