Tripodal metal complexes have been widely used for catalysis and more recently also for molecular recognition applications. Their ability in recognition and signal amplification of chiral substrates is because of the setup of the ligand around the metal in a propeller shape. Within this subject, we have recently reported tris(2-pyridylmethyl)amine- and triphenolamine-based complexes for the determination of the enantiomeric excess of various substrates. Herein, we show the versatility of the zinc tris(2-pyridylmethyl)amine-based stereodynamic probe by performing a detailed study of the imine formation process, by the extension of the sensing capabilities to other chiral compounds. A principal component analysis study of the system together with TD-DFT studies highlights the molecular origin of the observed chiroptical properties.
Extending substrate sensing capabilities of zinc tris(2-pyridylmethyl)amine-based stereodynamic probe
Badetti E.;Zonta C.
2019-01-01
Abstract
Tripodal metal complexes have been widely used for catalysis and more recently also for molecular recognition applications. Their ability in recognition and signal amplification of chiral substrates is because of the setup of the ligand around the metal in a propeller shape. Within this subject, we have recently reported tris(2-pyridylmethyl)amine- and triphenolamine-based complexes for the determination of the enantiomeric excess of various substrates. Herein, we show the versatility of the zinc tris(2-pyridylmethyl)amine-based stereodynamic probe by performing a detailed study of the imine formation process, by the extension of the sensing capabilities to other chiral compounds. A principal component analysis study of the system together with TD-DFT studies highlights the molecular origin of the observed chiroptical properties.File | Dimensione | Formato | |
---|---|---|---|
Chirality 2019.pdf
non disponibili
Descrizione: full text
Tipologia:
Versione dell'editore
Licenza:
Accesso chiuso-personale
Dimensione
964.73 kB
Formato
Adobe PDF
|
964.73 kB | Adobe PDF | Visualizza/Apri |
I documenti in ARCA sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.