Structural characterisation and photophysical properties of lanthanoid complexes of a tetra-amide functionalised calixarene
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Lanthanoid complexes of a tetra-amide substituted calixarene in the cone conformation are characterised by single crystal X-ray structure determination. The structural analysis shows that the metal ions are coordinated to the calixarene through the eight O donor atoms, along with one aqua ligand which is located within the cavity of the calixarene. The calixarene ligand was covalently incorporated into a polymethylmethacrylate monolith through p-allyl functional groups, followed by loading with a range of lanthanoid cations giving rise to light-emitting materials. The emission from the hydrid materials was found to be comparable to the solution phase emission.
This is an Author's Original Manuscript of an article published by Taylor & Francis in Supramolecular Chemistry on 29/01/2016 available online at <a href="http://www.tandfonline.com/10.1080/10610278.2015.1136744">http://www.tandfonline.com/10.1080/10610278.2015.1136744</a>