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

Jacob Filiti; Kyle Hearn; Elley Rudebeck; Huynh Thien Ngo; Nguyen-Nguyen Pham-Tran; Frederick Pfeffer

doi:10.1039/D1OB01664D

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

Jacob Filiti,^a Kyle Hearn,

^a Elley Rudebeck,

^a Huynh Thien Ngo,

^b Nguyen-Nguyen Pham-Tran

^c and Frederick Pfeffer

*^a

Author affiliations

* Corresponding authors

^a School of Life and Environmental Sciences, Deakin University, Waurn Ponds, Geelong, Australia
E-mail: fred.pfeffer@deakin.edu.au

^b Center for Functional Sensors & Actuators (CFSN), Research Center for Functional Materials, National Institute for Materials Science (NIMS), Tsukuba, Ibaraki 305-0044, Japan

^c Faculty of Chemistry, University of Science, Vietnam National University, Ho Chi Minh City, Vietnam

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.

This article is part of the themed collection: The Supramolecular Chemistry of Anions

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Article information

DOI: https://doi.org/10.1039/D1OB01664D
Article type: Paper
Submitted: 24 Aug 2021
Accepted: 08 Oct 2021
First published: 08 Oct 2021

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

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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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Organic & Biomolecular Chemistry

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

Abstract

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

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