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Pulsed Electron Decoupling and Strategies for Time Domain Dynamic Nuclear Polarization with Magic Angle Spinning.
Saliba, Edward P; Sesti, Erika L; Alaniva, Nicholas; Barnes, Alexander B.
Afiliação
  • Saliba EP; Department of Chemistry , Washington University in St. Louis , St. Louis , Missouri 63130 , United States.
  • Sesti EL; Department of Chemistry , Washington University in St. Louis , St. Louis , Missouri 63130 , United States.
  • Alaniva N; Department of Chemistry , Washington University in St. Louis , St. Louis , Missouri 63130 , United States.
  • Barnes AB; Department of Chemistry , Washington University in St. Louis , St. Louis , Missouri 63130 , United States.
J Phys Chem Lett ; 9(18): 5539-5547, 2018 Sep 20.
Article em En | MEDLINE | ID: mdl-30180584
ABSTRACT
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.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: J Phys Chem Lett Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Estados Unidos