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Spatial Distribution of Silica-Bound Catalytic Organic Functional Groups Can Now Be Revealed by Conventional and DNP-Enhanced Solid-State NMR Methods
Author(s) -
Takeshi Kobayashi,
Marek Pruski
Publication year - 2019
Publication title -
acs catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.898
H-Index - 198
ISSN - 2155-5435
DOI - 10.1021/acscatal.9b02017
Subject(s) - magic angle spinning , solid state nuclear magnetic resonance , catalysis , mesoporous material , materials science , context (archaeology) , solid state , molecule , nanotechnology , chemical physics , chemical engineering , chemistry , nuclear magnetic resonance spectroscopy , physics , nuclear magnetic resonance , organic chemistry , engineering , paleontology , biology
Understanding the spatial distribution of functionalities on surfaces with atomic-scale resolution is very important for catalytic applications, yet very challenging for analytical inquiry. Recent advances in solid-state nuclear magnetic resonance (SSNMR), especially in dynamic nuclear polarization and fast magic-angle spinning, offer new tools for examining this longstanding problem. The aim of this Perspective is to showcase how these SSNMR methods can shed light on the uniformity of surface functionalities deployed on mesoporous silica-based catalysts using post-synthesis grafting and co-condensation methods. The results are discussed in the context of earlier landmark studies on the spatial distributions of surface species using probe molecules and reactions.

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