Abstract
Halogen bonding between two negatively charged species, tetraiodo-p-benzoquinone anion radicals (I4Q−.) and iodide anions, was observed and characterized for the first time. X-ray structural and EPR/UV–Vis spectral studies revealed that the anion–anion bonding led to the formation of crystals comprising 2D layers of I4Q−. anion radicals linked by iodides and separated by Et4N+ counter-ions. Computational analysis suggested that the seemingly antielectrostatic halogen bonds in these systems were formed via a combination of several factors. First, an attenuation of the interionic repulsion by the solvent facilitated close approach of the anions leading to their mutual polarization. This resulted in the appearance of positively charged areas (σ-holes) on the surface of the iodine substituents in I4Q−. responsible for the attractive interaction. Finally, the solid-state associations were also stabilized by multicenter (4:4) halogen bonding between I4Q−. and iodide.
| Original language | English |
|---|---|
| Pages (from-to) | 17197-17201 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 59 |
| Issue number | 39 |
| DOIs | |
| State | Published - 21 Sep 2020 |
Bibliographical note
Publisher Copyright:© 2020 Wiley-VCH GmbH
Keywords
- halides
- halogen bonding
- quinones
- radical anions
- supramolecular chemistry
ASJC Scopus subject areas
- Catalysis
- General Chemistry