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Large Molecular Weight Nitroxide Biradicals Providing Efficient Dynamic Nuclear Polarization at Temperatures up to 200 K
Author(s) -
Alexandre Zagdoun,
Gilles Casano,
Olivier Ouari,
Martin Schwarzwälder,
Aaron J. Rossini,
Fabien Aussenac,
Maxim Yulikov,
Gunnar Jeschke,
Christophe Copéret,
Anne Lesage,
Paul Tordo,
Lyndon Emsley
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/ja405813t
Subject(s) - chemistry , nitroxide mediated radical polymerization , radical , polarization (electrochemistry) , analytical chemistry (journal) , electron , magic angle spinning , nuclear magnetic resonance , organic chemistry , nuclear magnetic resonance spectroscopy , polymerization , nuclear physics , physics , radical polymerization , polymer
A series of seven functionalized nitroxide biradicals (the bTbK biradical and six derivatives) are investigated as exogenous polarization sources for dynamic nuclear polarization (DNP) solid-state NMR at 9.4 T and with ca. 100 K sample temperatures. The impact of electron relaxation times on the DNP enhancement (ε) is examined, and we observe that longer inversion recovery and phase memory relaxation times provide larger ε. All radicals are tested in both bulk 1,1,2,2-tetrachloroethane solutions and in mesoporous materials, and the difference in ε between the two cases is discussed. The impact of the sample temperature and magic angle spinning frequency on ε is investigated for several radicals each characterized by a range of electron relaxation times. In particular, TEKPol, a bulky derivative of bTbK with a molecular weight of 905 g·mol(-1), is presented. Its high-saturation factor makes it a very efficient polarizing agent for DNP, yielding unprecedented proton enhancements of over 200 in both bulk and materials samples at 9.4 T and 100 K. TEKPol also yields encouraging enhancements of 33 at 180 K and 12 at 200 K, suggesting that with the continued improvement of radicals large ε may be obtained at higher temperatures.

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