RESUMEN
Monometallic gold(I)-alkynyl-helicene complexes (1 a,b) and bimetallic gold(I)-alkynyl-helicene architectures featuring the presence (2 a,b) or absence (3 a,b) of aurophilic intramolecular interactions were prepared by using different types of phosphole ligands (mono-phosphole L1 or bis-phospholes L2,3). The influence of the Au(I) d(10) metal center(s) on the electronic, photophysical, and chiroptical properties of these unprecedented phosphole-gold(I)-alkynyl-helicene complexes was examined. Experimental and theoretical results highlight the importance of ligand-to-ligand-type charge transfers and the strong effect of the presence or absence of Au(I) -Au(I) interactions in 2 a,b.
RESUMEN
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 πâ 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 πâ 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.
RESUMEN
Upon reaction with ligands A, 1 and 3 bearing the 2,5-bis(2-pyridyl)phosphole fragment, an unexpected conversion of Cu(II) metal centers to Cu(I) centers is observed affording either bimetallic complexes bearing a bridging phosphane coordination mode or hexametallic metallacycles.
