El Sayed Moussa Mehdi, Guillois Kevin, Shen Wenting, Réau Régis, Crassous Jeanne, Lescop Christophe
Institut des Sciences Chimiques de Rennes, UMR 6226 CNRS, Université de Rennes 1, Campus de Beaulieu, 35042 Rennes Cedex (France), Fax: (+33) 2-23-23-69-39.
Chemistry. 2014 Nov 3;20(45):14853-67. doi: 10.1002/chem.201403758. Epub 2014 Sep 18.
Reactions between the U-shaped binuclear Cu(I) complex A that bears short metal-metal distances and the cyano-capped monotopic π-conjugated ligands 1-5 that carry gradually bulkier polyaromatic terminal fragments lead to the formation of π-stacked supramolecular assemblies 6-10, respectively, in yields of 50-80 %. These derivatives have been characterized by multinuclear NMR spectroscopic analysis and X-ray diffraction studies. Their solid-state structures show the selective formation of U-shaped supramolecular assemblies in which two monotopic π-conjugated systems present large (6, 7, and 9) or medium (8 and 10) intramolecular π overlap, thus revealing π-π interactions. These assemblies self-organize into head-to-tail π-stacked dimers that in turn self-assemble to afford infinite columnar π stacks. The nature, extent, and complexity of the intermolecular contacts within the head-to-tail π-stacked dimer depend on the nature of the terminal polyaromatic fragment carried by the cyano-capped monotopic ligand, but it does not alter the result of the self-assembling process. These results demonstrate that the dinuclear molecular clip A that bears short metal-metal distances allows selective supramolecular assembly processes driven by the formation of intra- and intermolecular short π-π interactions in the resulting self-assembled structures; thus, demonstrating that their shape is not only dictated by the symmetry of the building blocks. This approach opens perspectives toward the formation of extended π-stacked columns based on dissymmetrical and functional π-conjugated systems.
具有短金属 - 金属距离的U形双核铜(I)配合物A与带有逐渐增大的多芳族末端片段的氰基封端的单齿π共轭配体1 - 5之间的反应分别导致形成π堆积的超分子组装体6 - 10,产率为50 - 80%。这些衍生物已通过多核NMR光谱分析和X射线衍射研究进行了表征。它们的固态结构显示出U形超分子组装体的选择性形成,其中两个单齿π共轭体系呈现大的(6、7和9)或中等的(8和10)分子内π重叠,从而揭示了π - π相互作用。这些组装体自组织成头对尾的π堆积二聚体,进而自组装形成无限的柱状π堆积。头对尾π堆积二聚体内分子间接触的性质、程度和复杂性取决于氰基封端的单齿配体携带的末端多芳族片段的性质,但它不会改变自组装过程的结果。这些结果表明,具有短金属 - 金属距离的双核分子夹A允许在所得自组装结构中通过形成分子内和分子间短π - π相互作用驱动选择性超分子组装过程;因此,表明它们的形状不仅由构建块的对称性决定。这种方法为基于不对称和功能性π共轭体系形成扩展的π堆积柱开辟了前景。