Probing a Hydrogen-π Interaction Involving a Trapped Water Molecule in the Solid State.
Ettore BartalucciAlexander A MalärAnne MehnertJulius B StückrathLennart GünzelMaik IckerMartin BörnerChristian WiebelerBeat H MeierStefan GrimmeBerthold KerstingThomas WiegandPublished in: Angewandte Chemie (International ed. in English) (2023)
The detection and characterization of trapped water molecules in chemical entities and biomacromolecules remains a challenging task for solid materials. We herein present proton-detected solid-state Nuclear Magnetic Resonance (NMR) experiments at 100 kHz magic-angle spinning and at high static magnetic-field strengths (28.2 T) enabling the detection of a single water molecule fixed in the calix[4]arene cavity of a lanthanide complex by a combination of three types of non-covalent interactions. The water proton resonances are detected at a chemical-shift value close to zero ppm, which we further confirm by quantum-chemical calculations. Density Functional Theory calculations pinpoint to the sensitivity of the proton chemical-shift value for hydrogen-π interactions. Our study highlights how proton-detected solid-state NMR is turning into the method-of-choice in probing weak non-covalent interactions driving a whole branch of molecular-recognition events in chemistry and biology.
Keyphrases
- solid state
- density functional theory
- molecular dynamics
- magnetic resonance
- molecular dynamics simulations
- single molecule
- loop mediated isothermal amplification
- high frequency
- high resolution
- label free
- monte carlo
- magnetic resonance imaging
- real time pcr
- decision making
- mass spectrometry
- quantum dots
- energy transfer