Evaluating surface interactions in supported imidazolium ionic liquid phases by using ultrasensitive DNP NMR and DFT studies

Handle

https://riunet.upv.es/handle/10251/237445

Cita bibliográfica

Chen, H.; Chacón-Rosales, Gustavo Javier; De Araujo, BB.; Goncalves, PFB.; Dos Santos, FP.; Kempf, JG.; Dupont, J. (2026). Evaluating surface interactions in supported imidazolium ionic liquid phases by using ultrasensitive DNP NMR and DFT studies. Physical Chemistry Chemical Physics. https://doi.org/10.1039/d6cp00111d

Titulación

Resumen

[EN] The intimate interaction between imidazolium-based ionic liquid (IL) salts, whether grafted or coated on silica, has been explored using low-temperature dynamic nuclear polarization (DNP) NMR and density functional theory (DFT) calculations. NMR experiments revealed interactions between resolved carbon sites on the IL and various silicon sites in the underlying surface. Such experiments are challenged by mere natural-abundance levels of C-13 (1.1%) and 29Si (4.7%) and the desire for specificity to only surface regions of the porous sample. DNP enhancements of >= 100 & times; provided excellent signal-to-noise ratios (SNRs) such that 2D NMR heteronuclear correlation (HETCOR) spectra of surface-associated molecules via both H-1-C-13 and H-1-Si-29 spectroscopy were obtained in <3 hours with SNRs of similar to 10-140 among various sites, as well as more structurally definitive direct C-13-Si-29 HETCOR with SNRs of similar to 5-10 in <3 days. These results would be impossible to obtain without noted DNP gains. These results reveal the interaction between IL and silica, whereas the NMR and DFT combination further explores the orientation of the IL with respect to the surface, altogether showing that grafting is necessary for a well-defined relationship with the silica surface. The overall results can provide guidance on structure-function relationships for applications of this class of materials in heterogeneous catalysis and beyond.

Fuente

Physical Chemistry Chemical Physics issn: 1463-9076

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