Organic & Biomolecular Chemistry · 2010 · 34 citations · 16 references
Natural SciencesChemistryPhysicsOrganic ChemistrySolid-state ChemistrySupramolecular ChemistryAnion RecognitionCoordination ChemistryLigand BindingOrganic Electronic MaterialsReceptor-ligand InteractionsSupramolecular MaterialsAnion - Pi InteractionsAnion Receptor DesignAnion-π InteractionsBoron ChemistryConjugated MoleculesOptical PropertiesPyrrole Chemistryπ Interactions
Substituents at the boron unit of dipyrrolyldiketone boron complexes as pi-conjugated acyclic anion receptors play crucial roles for the tuning of solid-state molecular assemblies, anion-binding behaviour and electronic and optical properties. In particular, emission quantum yields can be significantly tunable by boron substituents and pyrrole alpha-aryl moieties.
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Anion‐Responsive Supramolecular Gels
Hiromitsu Maeda · Chemistry - A European Journal · 2008 · 287 citations