Solvent-free dynamic nuclear polarization enhancements in organically modified mesoporous silica.


Journal

Physical chemistry chemical physics : PCCP
ISSN: 1463-9084
Titre abrégé: Phys Chem Chem Phys
Pays: England
ID NLM: 100888160

Informations de publication

Date de publication:
09 Jun 2021
Historique:
pubmed: 25 5 2021
medline: 25 5 2021
entrez: 24 5 2021
Statut: ppublish

Résumé

High-field dynamic nuclear polarization is a powerful tool for the structural characterization of species on the surface of porous materials or nanoparticles. For these studies the main source of polarization are radical-containing solutions which are added by post-synthesis impregnation of the sample. Although this strategy is very efficient for a wide variety of materials, the presence of the solvent may influence the chemistry of functional species of interest. Here we address the development of a comprehensive strategy for solvent-free DNP enhanced NMR characterization of functional (target) species on the surface of mesoporous silica (SBA-15). The strategy includes the partial functionalization of the silica surface with Carboxy-Proxyl nitroxide radicals and target Fmoc-Glycine functional groups. As a proof of principle, we have observed for the first time DNP signal enhancements, using the solvent-free approach, for 13C{1H} CPMAS signals corresponding to organic functionalities on the silica surface. DNP enhancements of up to 3.4 were observed for 13C{1H} CPMAS, corresponding to an experimental time save of about 12 times. This observation opens the possibility for the DNP-NMR study of surface functional groups without the need of a solvent, allowing, for example, the characterization of catalytic reactions occurring on the surface of mesoporous systems of interest. For 29Si with direct polarization NMR, up to 8-fold DNP enhancements were obtained. This 29Si signal enhancement is considerably higher than the obtained with similar approaches reported in literature. Finally, from DNP enhancement profiles we conclude that cross-effect is probably the dominant polarization transfer mechanism.

Identifiants

pubmed: 34027938
doi: 10.1039/d1cp00985k
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

12559-12568

Auteurs

Marcos de Oliveira (M)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de and São Carlos Institute of Physics, University of São Paulo, PO Box 369, 13560-970, São Carlos, SP, Brazil. mjunior@ifsc.usp.br.

Kevin Herr (K)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Martin Brodrecht (M)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Nadia B Haro-Mares (NB)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Till Wissel (T)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Vytautas Klimavicius (V)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de and Institute of Chemical Physics, Vilnius University, Sauletekio av. 3, LT-10257 Vilnius, Lithuania.

Hergen Breitzke (H)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Torsten Gutmann (T)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Gerd Buntkowsky (G)

Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.

Classifications MeSH