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Solid-Phase Polarization Matrixes for Dynamic Nuclear Polarization from Homogeneously Distributed Radicals in Mesostructured Hybrid Silica Materials
Author(s) -
David Gajan,
Martin Schwarzwälder,
Matthew P. Conley,
W Grüning,
Aaron J. Rossini,
Alexandre Zagdoun,
Moreno Lelli,
Maxim Yulikov,
Gunnar Jeschke,
Claire Sauvée,
Olivier Ouari,
Paul Tordo,
Laurent Veyre,
Anne Lesage,
Chloé Thieuleux,
Lyndon Emsley,
Christophe Copéret
Publication year - 2013
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja405822h
Subject(s) - chemistry , radical , polarization (electrochemistry) , covalent bond , mesoporous material , homogeneous , mesoporous silica , organic chemistry , catalysis , thermodynamics , physics
Mesoporous hybrid silica-organic materials containing homogeneously distributed stable mono- or dinitroxide radicals covalently bound to the silica surface were developed as polarization matrixes for solid-state dynamic nuclear polarization (DNP) NMR experiments. For TEMPO-containing materials impregnated with water or 1,1,2,2-tetrachloroethane, enhancement factors of up to 36 were obtained at ∼100 K and 9.4 T without the need for a glass-forming additive. We show that the homogeneous radical distribution and the subtle balance between the concentration of radical in the material and the fraction of radicals at a sufficient inter-radical distance to promote the cross-effect are the main determinants for the DNP enhancements we obtain. The material, as well as an analogue containing the poorly soluble biradical bTUrea, is used as a polarizing matrix for DNP NMR experiments of solutions containing alanine and pyruvic acid. The analyte is separated from the polarization matrix by simple filtration.

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