The binding affinities of tetramethylammonium chloride to uranyl salophen receptors decorated with X-substituted aromatic pendants (X ¼ OCH3, CH3, H, Br, NO2) point to the importance of resonance effects in cation-p interactions, at variance with the view that field/inductive effects play a dominant role.
Substituent effects in cation-p interactions. Recognition of tetramethylammonium chloride by uranyl-salophen receptors
A Dalla Cort;L Mandolini
2012
Abstract
The binding affinities of tetramethylammonium chloride to uranyl salophen receptors decorated with X-substituted aromatic pendants (X ¼ OCH3, CH3, H, Br, NO2) point to the importance of resonance effects in cation-p interactions, at variance with the view that field/inductive effects play a dominant role.File in questo prodotto:
Non ci sono file associati a questo prodotto.
I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
