Branching-Chain Propagation of Parahydrogen-Derived Nuclear Spin Order on a Catalyst Surface.
Ekaterina V PokochuevaDudari B BuruevaOleg G SalnikovIgor V KoptyugPublished in: Chemphyschem : a European journal of chemical physics and physical chemistry (2024)
This study reveals that, when two hydrogen atoms are produced on the surface of a catalyst (e. g., a metal nanoparticle) upon dissociation of a parahydrogen molecule, their initial nuclear spin correlation can propagate in a branching-chain fashion as they diffuse and combine with random H atoms to produce H 2 molecules, which subsequently dissociate. This process leads to a gradual dilution of the non-equilibrium nuclear spin order, but the number of involved H atoms that share the spin order becomes larger. These conclusions, confirmed by the spin density matrix calculations, may be relevant in the context of parahydrogen-induced polarization (PHIP) in heterogeneous hydrogenations catalyzed by supported metal catalysts, the observation of which apparently contradicts the accepted non-pairwise mechanism of the addition of hydrogen to an unsaturated substrate over such catalysts. The potential consequences of the reported findings are discussed in the context of PHIP effects and beyond.
Keyphrases
- room temperature
- density functional theory
- transition metal
- ionic liquid
- molecular dynamics
- highly efficient
- single molecule
- metal organic framework
- molecular dynamics simulations
- gold nanoparticles
- diabetic rats
- high glucose
- low grade
- mass spectrometry
- reduced graphene oxide
- liquid chromatography tandem mass spectrometry
- ms ms
- oxidative stress
- drug induced
- human health