Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization

Synthesis of novel trityl-nitroxyl biradicals and their performance as polarization agents in DNP-enhanced solid-state MAS NMR spectroscopy is presented. Signal enhancements in 1H, 1H → 13C CP MAS, and 13C MAS experiments obtained with these radicals dissolved in 1,1,2,2-tetrachloroethane (TCE) solu...

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Veröffentlicht in:Journal of physical chemistry. C 2018-05, Vol.122 (21), p.11422-11432
Hauptverfasser: Bothe, Sarah, Nowag, Jens, Klimavičius, Vytautas, Hoffmann, Markus, Troitskaya, Tatiana I, Amosov, Evgenii V, Tormyshev, Victor M, Kirilyuk, Igor, Taratayko, Andrey, Kuzhelev, Andrey, Parkhomenko, Dmitriy, Bagryanskaya, Elena, Gutmann, Torsten, Buntkowsky, Gerd
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container_end_page 11432
container_issue 21
container_start_page 11422
container_title Journal of physical chemistry. C
container_volume 122
creator Bothe, Sarah
Nowag, Jens
Klimavičius, Vytautas
Hoffmann, Markus
Troitskaya, Tatiana I
Amosov, Evgenii V
Tormyshev, Victor M
Kirilyuk, Igor
Taratayko, Andrey
Kuzhelev, Andrey
Parkhomenko, Dmitriy
Bagryanskaya, Elena
Gutmann, Torsten
Buntkowsky, Gerd
description Synthesis of novel trityl-nitroxyl biradicals and their performance as polarization agents in DNP-enhanced solid-state MAS NMR spectroscopy is presented. Signal enhancements in 1H, 1H → 13C CP MAS, and 13C MAS experiments obtained with these radicals dissolved in 1,1,2,2-tetrachloroethane (TCE) solution are compared with the enhancements obtained from TCE solutions of binitroxyl radicals. The signal enhancements are correlated with the distance between the radical centers of the biradicals, as determined by theoretical structure calculations. Some of the biradical TCE solutions display direct-channel resonances in 13C MAS experiments as well as indirect channel resonances induced via the proton spin reservoir. Differential scanning calorimetry reveals that only these solutions do not form any solid crystalline phases upon rapid cooling, suggesting that molecular motions needed for polarization transfer from radicals to 13C via the proton spin reservoir remain active at the experimental low temperatures of nominal 120 K. DNP magnetic field sweep enhancement profiles for selected new biradicals are presented as well. These indicate that the DNP transfer is dominated by the cross-effect mechanism.
doi_str_mv 10.1021/acs.jpcc.8b02570
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Differential scanning calorimetry reveals that only these solutions do not form any solid crystalline phases upon rapid cooling, suggesting that molecular motions needed for polarization transfer from radicals to 13C via the proton spin reservoir remain active at the experimental low temperatures of nominal 120 K. DNP magnetic field sweep enhancement profiles for selected new biradicals are presented as well. 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title Novel Biradicals for Direct Excitation Highfield Dynamic Nuclear Polarization
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