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Spatial distribution of organic functional groups supported on mesoporous silica nanoparticles: a study by conventional and DNP-enhanced 29Si solid-state NMR
Author(s) -
Takeshi Kobayashi,
Dilini SingappuliArachchige,
Zhuoran Wang,
Igor I. Slowing,
Marek Pruski
Publication year - 2016
Publication title -
physical chemistry chemical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.053
H-Index - 239
eISSN - 1463-9084
pISSN - 1463-9076
DOI - 10.1039/c6cp07642d
Subject(s) - mesoporous material , nanoparticle , mesoporous silica , solid state , grafting , solid state nuclear magnetic resonance , materials science , chemical engineering , nanotechnology , chemistry , nuclear magnetic resonance , organic chemistry , catalysis , polymer , physics , engineering , composite material
Solid-state NMR spectroscopy, both conventional and dynamic nuclear polarization (DNP)-enhanced, was employed to study the spatial distribution of organic functional groups attached to the surface of mesoporous silica nanoparticles via co-condensation and grafting. The most revealing information was provided by DNP-enhanced two-dimensional 29 Si- 29 Si correlation measurements, which unambiguously showed that post-synthesis grafting leads to a more homogeneous dispersion of propyl and mercaptopropyl functionalities than co-condensation. During the anhydrous grafting process, the organosilane precursors do not self-condense and are unlikely to bond to the silica surface in close proximity (less than 4 Å) due to the limited availability of suitably arranged hydroxyl groups.

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