Issue 42, 2021

Comparing the anion binding of 4-amido- with 4-amino-1,8-naphthalimides

Abstract

The synthesis and evaluation of a new anion receptor based on the 4-amido-1,8-naphthalimide scaffold is described. The findings indicate that the amide N–H is an enhanced H-bond donor but is otherwise restricted in its ability to participate in the binding of simple anions.

Graphical abstract: Comparing the anion binding of 4-amido- with 4-amino-1,8-naphthalimides

Supplementary files

Article information

Article type
Paper
Submitted
24 Aug. 2021
Accepted
08 Okt. 2021
First published
08 Okt. 2021

Org. Biomol. Chem., 2021,19, 9260-9265

Comparing the anion binding of 4-amido- with 4-amino-1,8-naphthalimides

J. Filiti, K. Hearn, E. Rudebeck, H. T. Ngo, N. Pham-Tran and F. Pfeffer, Org. Biomol. Chem., 2021, 19, 9260 DOI: 10.1039/D1OB01664D

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