Showing papers by "J. Fraser Stoddart published in 1986"

Second‐Sphere Coordination–a Novel Rǒle for Molecular Receptors

Abstract: Although it has been appreciated for most of this century that the coordinating influence of many transition metal complexes extends beyond their covalently-bonded first-sphere ligands to non-covalently bound chemical species in the so-called second-sphere, it is only recently that the fundamental importance of the phenomenon has been recognized and researched in its most general context. Rapid progress has been possible in this relatively new area of supramolecular chemistry by appealing to the symbiotic relationship that exists between X-ray crystallographic investigations and synthetic work. The gamut of non-covalent bonds, including electrostatic forces, hydrogen bonding, charge transfer, and van der Waals interactions are available for exploitation in choosing or designing suitable molecular receptors for particular transition metal complexes. Crown ethers are the synthetic macrocycles par excellence for forming adducts with neutral and cationic complexes carrying protic ligands (NH3, H2O, CH3CN, etc.) in their first coordination spheres. Anionic complexes with electron-rich first-sphere ligands (e.g. CN⊖) form adducts with polyammonium macrocyclic receptors. In both situations, hydrogen bonds and electrostatic interactions provide the dominant sources of supramolecular stabilization. Spectroscopic studies (UV, IR, and NMR) reveal that the structural integrity of the adducts is usually maintained in solution. The transition metal complexes can be organometallic as well as inorganic. In complexes supporting organic ligands, such as 1,5-cyclooctadiene, norbornadiene, cyclopentadiene, 2,2′-bipyridine, and trimethylphosphane, the opportunity exists to match their steric and electronic characteristics with appropriate binding sites in the molecular receptor. With these ligands, the weaker categories of non-covalent bonding, e.g. charge transfer and van der Waals interactions, assume considerable importance. The phenomenon is also observable with naturally-occurring receptors such as the cyclodextrins and polyether antibiotics. Moreover, it extends beyond the territory of transition metal complexes to main group complexes such as ammonia-borane. As far as applications are concerned, it finds expression in areas as diverse as separation science and drug delivery systems.

Isolation and X-ray crystal structure of a 2:1 complex between picric acid and dibenzo-24-crown-8; an example of a sandwich structure

Abstract: Despite the lack of strong intermolecular interactions in solution, picric acid (PicH) forms crystalline 2:1 complexes with both dibenzo-18-crown-6 (DB18C6) and dibenzo-24-crown-8 (DB24C8). An X-ray crystallographic study of 2PicH·DB24C8 reveals a continous layer structure comprising alternate PicH and DB24C8 molecules with stacking of the π-electron-deficient aromatic rings in the PicH molecules and the π-electron-rich aromatic rings in DB24C8 molecules.