Abstract

Reaction of an excess of hydrated LnCl 3 (Ln = La, Gd, Ho, Yb, Y) with sodium 5-(2-pyridyl)tetrazolate (Na pytz) in water led to the formation of either cationic disubstituted complexes (La, Gd, Ho) or neutral μ-hydroxo-bridged dimers (Y, Yb). Interestingly, there is a lack of propensity for these disubstituted complexes to redistribute forming trisubstituted ones, which is a common behaviour in lanthanoid chemistry. Also, compared to their corresponding lanthanoid carboxylates, all these products are discrete molecular entities forming an extensive hydrogen-bonded and/or π stacking network rather than hybrid polymeric frameworks.

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