Examples of reactivity of carbonyl and phosphoryl compounds controlled by calixarenes are illustrated in this review article. The molecular framework of calixarenes has been widely used as a versatile molecular platform for the dynamic arrangement of one or more structural units working as recognition and/or catalytic sites, in many cases with considerable levels of cooperation. The calixarene cavity itself has also been involved as a recognition unit for inclusion of the substrate or of part-structures of the substrate. Unique reactivity patterns of carbonyl or phosphoryl functional groups organised at the upper or lower rim of calixarenes will also be illustrated.

Cacciapaglia, R., Di Stefano, S., Mandolini, L., Salvio, R. (2013). Reactivity of carbonyl and phosphoryl groups at calixarenes. SUPRAMOLECULAR CHEMISTRY, 25(9-11), 537-554 [10.1080/10610278.2013.824578].

Reactivity of carbonyl and phosphoryl groups at calixarenes

Salvio R.
2013-01-01

Abstract

Examples of reactivity of carbonyl and phosphoryl compounds controlled by calixarenes are illustrated in this review article. The molecular framework of calixarenes has been widely used as a versatile molecular platform for the dynamic arrangement of one or more structural units working as recognition and/or catalytic sites, in many cases with considerable levels of cooperation. The calixarene cavity itself has also been involved as a recognition unit for inclusion of the substrate or of part-structures of the substrate. Unique reactivity patterns of carbonyl or phosphoryl functional groups organised at the upper or lower rim of calixarenes will also be illustrated.
2013
Pubblicato
Rilevanza internazionale
Articolo
Esperti anonimi
Settore CHIM/07 - FONDAMENTI CHIMICI DELLE TECNOLOGIE
English
Con Impact Factor ISI
catalysis; enzyme mimics; host-guest; guanidinium; metal ion
Cacciapaglia, R., Di Stefano, S., Mandolini, L., Salvio, R. (2013). Reactivity of carbonyl and phosphoryl groups at calixarenes. SUPRAMOLECULAR CHEMISTRY, 25(9-11), 537-554 [10.1080/10610278.2013.824578].
Cacciapaglia, R; Di Stefano, S; Mandolini, L; Salvio, R
Articolo su rivista
File in questo prodotto:
File Dimensione Formato  
Supramolecular Chemistry 2013.pdf

solo utenti autorizzati

Tipologia: Versione Editoriale (PDF)
Licenza: Copyright dell'editore
Dimensione 656.76 kB
Formato Adobe PDF
656.76 kB Adobe PDF   Visualizza/Apri   Richiedi una copia

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2108/247727
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 25
  • ???jsp.display-item.citation.isi??? 21
social impact