Issue 14, 2020

Anion templated crystal engineering of halogen bonding tripodal tris(halopyridinium) compounds

Abstract

In this work four new tripodal tris(halopyridinium) receptors containing potentially halogen bonding groups were prepared. The ability of the receptors to bind anions in competitive CD3CN/d6-DMSO was studied using 1H NMR titration experiments, which revealed that the receptors bind chloride anions more strongly than more basic acetate or other halide ions. The solid state self-assembly of the tripodal receptors with halide anions was investigated by X-ray crystallography. The nature of the structures was dependent on the choice of halide anion, as well as the crystallisation solvent. Halogen bond lengths as short as 80% of the sum of the van der Waals radii were observed, which is shorter than any halogen bonds involving halopyridinium receptors in the Cambridge Structural Database.

Graphical abstract: Anion templated crystal engineering of halogen bonding tripodal tris(halopyridinium) compounds

Supplementary files

Article information

Article type
Paper
Submitted
18 Feb 2020
Accepted
08 Mar 2020
First published
24 Mar 2020

CrystEngComm, 2020,22, 2526-2536

Anion templated crystal engineering of halogen bonding tripodal tris(halopyridinium) compounds

É. M. Foyle and N. G. White, CrystEngComm, 2020, 22, 2526 DOI: 10.1039/D0CE00241K

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements