Addition of metal salts to a diiridium macrocyclic complex leads the spontaneous formation supramolecular particles that react preferentially with small substrates and can tolerate glutathione additives.

Macrocyclic ligands form highly selective and kinetically labile complexes with a wide range of cations, including alkali metal and alkaline earth cations. Formation rate constants are high and remarkably insensitive to ligand structure, but decrease systematically with increasing charge density of the cation this behaviour is qualitatively similar to that expected for the dissociative intercha...

posed of a-1,4-linked glucose units, and a-, band g-CD, which are composed of 6, 7 and 8 glucose units, have been well studied and used in various fields because of their inclusion complex formation ability. However, their cavities are too small to form inclusion complexes with large guest molecules with molecular weights higher than several hundred. Large-ring CDs (LR-CDs) composed of more tha...

The field of heteropolymetallic complexes is of current interest in connection with the structures and roles of polymetallic active sites in biological systems [1], and the design of new molecular materials with magnetic, optical and electrical properties [2,3]. Among various relevant systems, oxamido-bridged polynuclear complexes [2,4] and phenolato-oxygen-bridged macrocyclic complexes [5,6] r...

The precise analysis of redox chemistry of MN4-based macrocyclic complexes is of great importance because of stabilization of unusual oxidation states of metal ions by macrocyclic ligand and thus have various applications in biochemistry, electrochemistry, electrocatalysis, pharmaceuticals etc. In this work, MN4-macrocyclic complexes of Co (II) and Ni(II) transition metal ...

Compared to structurally related linear trialkylamines, a simple macrocyclic amine with an anion-binding cavity exhibits very large rate enhancements (>10(5)) for stoichiometric N-alkylation with primary alkyl, allyl, and benzyl halides in the weakly polar solvent CDCl3. There is also a major distortion of the halide leaving-group order. For example, with benzyl halides the relative leaving-gro...

The macrocyclic 5,5,7,12,12,14-hexamethyl-1,4,8,11-tetraazacyclotetradeca-7,14-dienium bromide salt (LBr) was synthesisedfor use in complexationreactions with various metal salts of copper, nickel, and zinc. Twelve complexes were synthesised; five of them were successfully obtained in a crystal form that was suitable for X-ray crystallographic analysis. All the complexes were analysedby microel...

Large area uniform nanofibers have been fabricated from a hexameric arylene-ethynylene macrocycle (1) through in situ self-assembly on a glass substrate during solvent evaporation. The fibril morphology is controlled by the solvophilic core of 1, in conjunction with the interfacial interactions between the side chains of 1 and the substrate.

The title compound, [Ni(C6H4NO2)2(C16H38N6)], was prepared through self-assembly of a nickel(II) aza-macrocyclic complex with isonicotinic acid. The Ni(II) atom is located on an inversion center and exhibits a distorted octa-hedral N4O2 coordination environment, with the four secondary N atoms of the aza-macrocyclic ligand in the equatorial plane [average Ni-Neq = 2.064 (11) Å] and two O atoms ...

The synthesis of a new macrocyclic chelator incorporating a benzimidazole heterocycle is reported. Lanthanide complexes with macrocyclic chelators based on 1,4,7,10-tetra(carboxymethyl)-1,4,7,10-tetraazacyclododecane (DOTA) and 1,4,7-tris(carboxymethyl)-1,4,7,10-tetraazacyclododecane (DO3A) are of interest in luminescent, radiopharmaceutical and magnetic resonance (MR) biomedical imaging applic...