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Intramolecular rearrangement for regioselective complexation by intramolecular CH/pi interaction in a hydrophobic cavity of a ruthenium coordination sphere.

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A Ru(II) complex with a hydrophobic cavity formed from two 1-naphthoylamide groups was prepared. Its reactions with beta-diketones gave beta-diketonato complexes in which hydrophobic pi-pi or CH/pi interactions were confirmed by NMR spectroscopy and X-ray crystallography. In the case of the

The 3rd degree of biomimetism: associating the cavity effect, ZnII coordination and internal base assistance for guest binding and activation.

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The synthesis and characterization of a resorcinarene-based tetra(imidazole) ligand is reported. The properties of the corresponding ZnII complex are studied in depth, notably by NMR spectroscopy. In MeCN, acid-base titration reveals that one out of the four imidazole arms is hemi-labile and can be

Cerium-based triple-stranded helicates as luminescent chemosensors for the selective sensing of magnesium ions.

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Cerium-based triple-strand helicates Ce-CL(1) and Ce-CL(2) were achieved via self-assembly from malonohydrazone derived bis-tridentate ligands H(2)CL(1) and H(2)CL(2), respectively. Structure analysis of Ce-CL(1) shows that six oxygen atoms of the β-diketone groups on the ligands form a lantern-like

Triangles and tetrahedra: metal directed self-assembly of metallo-supramolecular structures incorporating bis-beta-diketonato ligands.

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The interaction of six aryl-linked bis-beta-diketones, including a new naphthylene linked species, with copper(II), iron(III) and, in one instance gallium(III), has been investigated with the aim of obtaining metallo-supramolecular assemblies exhibiting different geometries. New examples of two

Specific cooperative effect of a macrocyclic receptor for metal ion transfer into an ionic liquid.

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An intramolecular cooperative extraction system for the removal of strontium cations (Sr(2+)) from water by use of a novel macrocyclic receptor (H(2)βDA18C6) composed of diaza-18-crown-6 and two β-diketone fragments in ionic liquid (IL) is reported, together with X-ray spectroscopic characterization

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