Pulsed Electron Decoupling and Strategies for Time Domain Dynamic Nuclear Polarization with Magic Angle Spinning
Author(s) -
Edward P. Saliba,
Erika L. Sesti,
Nicholas Alaniva,
Alexander B. Barnes
Publication year - 2018
Publication title -
the journal of physical chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.563
H-Index - 203
ISSN - 1948-7185
DOI - 10.1021/acs.jpclett.8b01695
Subject(s) - spins , magic angle spinning , decoupling (probability) , electron , pulsed epr , polarization (electrochemistry) , microwave , nuclear magnetic resonance , time domain , atomic physics , spinning , materials science , physics , chemistry , nuclear magnetic resonance spectroscopy , condensed matter physics , spin echo , magnetic resonance imaging , computer science , medicine , quantum mechanics , control engineering , engineering , composite material , computer vision , radiology
Magic angle spinning (MAS) dynamic nuclear polarization (DNP) is widely used to increase nuclear magnetic resonance (NMR) signal intensity. Frequency-chirped microwaves yield superior control of electron spins and are expected to play a central role in the development of DNP MAS experiments. Time domain electron control with MAS has considerable promise to improve DNP performance at higher fields and temperatures. We have recently demonstrated that pulsed electron decoupling using frequency-chirped microwaves improves MAS DNP experiments by partially attenuating detrimental hyperfine interactions. The continued development of pulsed electron decoupling will enable a new suite of MAS DNP experiments that transfer polarization directly to observed spins. Time domain DNP transfers to nuclear spins in conjunction with pulsed electron decoupling is described as a viable avenue toward DNP-enhanced, high-resolution NMR spectroscopy over a range of temperatures from <6 to 320 K.
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