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Solvent-free dynamic nuclear polarization enhancements in organically modified mesoporous silica.
de Oliveira, Marcos; Herr, Kevin; Brodrecht, Martin; Haro-Mares, Nadia B; Wissel, Till; Klimavicius, Vytautas; Breitzke, Hergen; Gutmann, Torsten; Buntkowsky, Gerd.
Afiliação
  • 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.
  • Herr K; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • Brodrecht M; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • Haro-Mares NB; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • Wissel T; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • 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.
  • Breitzke H; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • Gutmann T; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
  • Buntkowsky G; Institut für Physikalische Chemie, Technische Universität Darmstadt, 64287 Darmstadt, Germany. gerd.buntkowsky@chemie.tu-darmstadt.de.
Phys Chem Chem Phys ; 23(22): 12559-12568, 2021 Jun 09.
Article em En | MEDLINE | ID: mdl-34027938
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Phys Chem Chem Phys Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Phys Chem Chem Phys Assunto da revista: BIOFISICA / QUIMICA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil