This short review highlights recent results in the chemistry of nonsymmetrically substituted uranyl-salophen complexes with specific reference to their synthesis and properties. Their use as receptors and catalysts is also emphasized. The possibility of modulating their structure within wide limits by choosing the proper substituted aldehydes and/or ketones as starting materials, coupled with their inherent chirality offers new appealing opportunities for their applications.

Nonsymmetrically substituted uranyl-salophen receptors: New opportunities for molecular recognition and catalysis / DALLA CORT, Antonella; Pasquini, Chiara; Luca, Schiaffino. - In: SUPRAMOLECULAR CHEMISTRY. - ISSN 1061-0278. - STAMPA. - 19:1-2(2007), pp. 79-87. [10.1080/10610270600977714]

Nonsymmetrically substituted uranyl-salophen receptors: New opportunities for molecular recognition and catalysis

DALLA CORT, Antonella;PASQUINI, CHIARA;
2007

Abstract

This short review highlights recent results in the chemistry of nonsymmetrically substituted uranyl-salophen complexes with specific reference to their synthesis and properties. Their use as receptors and catalysts is also emphasized. The possibility of modulating their structure within wide limits by choosing the proper substituted aldehydes and/or ketones as starting materials, coupled with their inherent chirality offers new appealing opportunities for their applications.
2007
inherent chirality; nonsymmetrical salophen ligands; schiff base complexes; uranyl ion; uranyl tetradentate; uranyl tetradentate schiff base complexes
01 Pubblicazione su rivista::01a Articolo in rivista
Nonsymmetrically substituted uranyl-salophen receptors: New opportunities for molecular recognition and catalysis / DALLA CORT, Antonella; Pasquini, Chiara; Luca, Schiaffino. - In: SUPRAMOLECULAR CHEMISTRY. - ISSN 1061-0278. - STAMPA. - 19:1-2(2007), pp. 79-87. [10.1080/10610270600977714]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11573/361547
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