Up to 100% Improvement in Dynamic Nuclear Polarization Solid-State NMR Sensitivity Enhancement of Polymers by Removing Oxygen
Investigating the efficiency of silica materials with wall-embedded nitroxide radicals for dynamic nuclear polarisation NMR
Supercritical CO2 impregnation process applied to polymer samples preparation for dynamic nuclear polarization solid-state NMR
Suppressing background signals in solid state NMR via the Electronic Mixing-Mediated Annihilation (EMMA) method
Towards measurement of homonuclear dipolar couplings in H-1 solid-state NMR: recoupling with a rotor-synchronized decoupling scheme
Quantitative Structural Constraints for Organic Powders at Natural Isotopic Abundance Using Dynamic Nuclear Polarization Solid-State NMR Spectroscopy
Improved Structural Elucidation of Synthetic Polymers by Dynamic Nuclear Polarization Solid-State NMR Spectroscopy
Probing crystal packing of uniformly C-13-enriched powder samples using homonuclear dipolar coupling measurements
Optimizing Sample Preparation Methods for Dynamic Nuclear Polarization Solid-state NMR of Synthetic Polymers
Observing Apparent Nonuniform Sensitivity Enhancements in Dynamic Nuclear Polarization Solid-State NMR Spectra of Polymers
A convenient method for the measurements of transverse relaxation rates in homonuclear scalar coupled spin systems
Probing the Motional Behavior of Eumelanin and Pheomelanin with Solid-State NMR Spectroscopy: New Insights into the Pigment Properties
Determining carbon-carbon connectivities in natural abundance organic powders using dipolar couplings
MRI assessment of multiple dipolar relaxation time (T1D) components in biological tissues interpreted with a generalized inhomogeneous magnetization transfer (ihMT) model.
Monitoring Crystallization Processes in Confined Porous Materials by Dynamic Nuclear Polarization Solid-State Nuclear Magnetic Resonance
Insights into the Crystallization and Structural Evolution of Glycine Dihydrate by In Situ Solid-State NMR Spectroscopy
A Strategy for Probing the Evolution of Crystallization Processes by Low-Temperature Solid-State NMR and Dynamic Nuclear Polarization.
Reducing the computational cost of NMR crystallography of organic powders at natural isotopic abundance with the help of 13 C-13 C dipolar couplings.
