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Carbon Dioxide Fixation and Sulfate Sequestration by a Supramolecular Trigonal Bipyramid
Authors:Dr. Colm Browne  William J. Ramsay  Dr. Tanya K. Ronson  John Medley‐Hallam  Prof. Jonathan R. Nitschke
Affiliation:1. University of Cambridge, Department of Chemistry, Lensfield Road, Cambridge, CB2 1EW (UK) http://www‐jrn.ch.cam.ac.uk/;2. Current address: School of Chemistry, University of Manchester, Oxford Road, Manchester, M13 9PL (UK)
Abstract:The subcomponent self‐assembly of a bent dialdehyde ligand and different cationic and anionic templates led to the formation of two new metallosupramolecular architectures: a FeII4L6 molecular rectangle was isolated following reaction of the ligand with iron(II) tetrafluoroborate, and a M5L6 trigonal bipyramidal structure was constructed from either zinc(II) tetrafluoroborate or cadmium(II) trifluoromethanesulfonate. The spatially constrained arrangement of the three equatorial metal ions in the M5L6 structures was found to induce small‐molecule transformations. Atmospheric carbon dioxide was fixed as carbonate and bound to the equatorial metal centers in both the Zn5L6 and Cd5L6 assemblies, and sulfur dioxide was hydrated and bound as the sulfite dianion in the Zn5L6 structure. Subsequent in situ oxidation of the sulfite dianion resulted in a sulfate dianion bound within the supramolecular pocket.
Keywords:carbon dioxide fixation  host–  guest systems  small‐molecule transformations  supramolecular chemistry  template synthesis
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