4.3 Article

Dynamic Nuclear Polarization enhanced NMR at 187 GHz/284 MHz using an Extended Interaction Klystron amplifier

Journal

JOURNAL OF MAGNETIC RESONANCE
Volume 265, Issue -, Pages 77-82

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.jmr.2016.01.021

Keywords

Dynamic Nuclear Polarisation; Quasi-optic microwaves; Extended Interaction Klystron amplifier

Funding

  1. EPSRC (U.K.) [EP/K011944/1]
  2. JRA7 consortium [HPR1-2001-50065, R113-CT-2003-505925]
  3. EPSRC [EP/K011944/1] Funding Source: UKRI
  4. Engineering and Physical Sciences Research Council [EP/K011944/1] Funding Source: researchfish

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A Dynamic Nuclear Polarisation (DNP) enhanced solid-state Magic Angle Spinning (MAS) NMR spectrometer which uses a 187 GHz (corresponding to H-1 NMR frequency of 284 MHz) Extended Interaction Klystron (EIK) amplifier as the microwave source is briefly described. Its performance is demonstrated for a biomolecule (bacteriorhodopsin), a pharmaceutical, and surface functionalised silica. The EIK is very compact and easily incorporated into an existing spectrometer. The bandwidth of the amplifier is sufficient that it obviates the need for a sweepable magnetic field, once set, for all commonly used radicals. The variable power (CW or pulsed) output from the EIK is transmitted to the DNP-NMR probe using a quasi-optic system with a high power isolator and a corrugated waveguide which feeds the microwaves into the DNP-NMR probe. Curved mirrors inside the probe project the microwaves down the axis of the MAS rotor, giving a very efficient system such that maximum DNP enhancement is achieved with less than 3 W output from the microwave source. The DNP-NMR probe operates with a sample temperature down to 90 K whilst spinning at 8 kHz. Significant enhancements, in excess of 100 for bacteriorhodopsin in purple membrane (bR in PM), are shown along with spectra which are enhanced by approximate to 25 with respect to room temperature, for both the pharmaceutical furosemide and surface functionalised silica. These enhancements allow hitherto prohibitively time consuming experiments to be undertaken. The power at which the DNP enhancement in bR in PM saturates does not change significantly between 90 K and 170 K even though the enhancement drops by a factor of approximate to 11. As the DNP build up time decreases by a factor 3 over this temperature range, the reduction in T-1n, is presumably a significant contribution to the drop in enhancement. (C) 2016 The Authors. Published by Elsevier Inc.

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