Pushing the Limits of Characterising a Weak Halogen Bond in Solution

Detection and characterisation of very weak, non-covalent interactions in solution is inherently challenging. Low affinity, short complex lifetime and a constant battle against entropy brings even the most sensitive spectroscopic methods to their knees. Herein we introduce a strategy for the accurate experimental description of weak chemical forces in solution. Its scope is demonstrated by the detailed geometric and thermodynamic characterisation of the weak halogen bond of a non-fluorinated aryl iodide and an ether oxygen (0.6 kJ mol(-1)). Our approach makes use of the entropic advantage of studying a weak force intramolecularly, embedded into a cooperatively folding system, and of the combined use of NOE- and RDC-based ensemble analyses to accurately describe the orientation of the donor and acceptor sites. Thermodynamic constants (Delta G, Delta H and Delta S), describing the specific interaction, were derived from variable temperature chemical shift analysis. We present a methodology for the experimental investigation of remarkably weak halogen bonds and other related weak forces in solution, paving the way for their improved understanding and strategic use in chemistry and biology.

Automated summary

This article presents a strategy for accurately describing weak chemical forces in solution, demonstrating the geometric and thermodynamic characterization of the weak halogen bond. By using a combination of NOE- and RDC-based ensemble analyses, this methodology allows for the precise orientation of donor and acceptor sites to be determined, paving the way for improved understanding and strategic use of weak forces in chemistry and biology.