The hydration behaviour of coordination complexes is important for understanding their roles as bio-imaging agents. Determination of hydration is difficult, and various optical and NMR-based techniques have been used. Here we use EPR spectroscopy to unambiguously demonstrate that a -butyl-pyridyl-functionalised Er DOTA derivative coordinates water, while its methylphosphinate analogue does not.
View Article and Find Full Text PDFSubstituted dysprosocenium complexes of the type [Dy(Cp)] exhibit slow magnetic relaxation at cryogenic temperatures and have emerged as top-performing single-molecule magnets. The remarkable properties of these compounds derive in part from the strong axial ligand field afforded by the cyclopentadiene anions, and the design of analogous compounds with even stronger ligand fields is one promising route toward identifying new single-molecule magnets that retain a magnetic memory at even higher temperatures. Here, we report the synthesis and characterization of a dysprosium bis(borolide) compound, [K(18-crown-6)][Dy(BCPh)] (), featuring the dysprosocenate anion [Dy(BCPh)] with a pseudoaxial coordination environment afforded by two dianionic pentaphenyl borolide ligands.
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