Rearrangement of Imidazolidine to Piperazine Rings in the Presence of DyIII

The formation of imidazolidines from secondary amines and aldehydes is well known. This small cycle can act as a nitrogen donor, and it is usually stable when it coordinates to metal ions. Sometimes, imidazolidines acting as ligands undergo breaking of the C-N bond when coordinating to the metal cen...

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Bibliographic Details
Published in:Chemistry Proceedings Vol. 12; no. 1; p. 30
Main Authors: Julio Corredoira-Vázquez, Paula Oreiro-Martínez, Ana M. García Deibe, Jesús Sanmartín-Matalobos, Matilde Fondo
Format: Journal Article
Language:English
Published: MDPI AG 01.11.2022
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ISSN:2673-4583
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Summary:The formation of imidazolidines from secondary amines and aldehydes is well known. This small cycle can act as a nitrogen donor, and it is usually stable when it coordinates to metal ions. Sometimes, imidazolidines acting as ligands undergo breaking of the C-N bond when coordinating to the metal center, yielding related amines. However, the reorganization of the imidazolidine into a piperazine ring is quite an unusual process. In this work, we describe the transformation of a zinc complex with a ligand containing two imidazolidine moieties into a zinc complex with a piperazine fragment as donor, in the presence of a dysprosium salt.
ISSN:2673-4583
DOI:10.3390/ecsoc-26-13547