Very high frequency (263 GHz) pulse EPR spectroscopy of high spin transition metal centers
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Updated: Oct 31, 2026

Site Directed Spin Labeling and EPR Spectroscopic Studies of Pentameric Ligand-Gated Ion Channels
Published on: July 4, 2016
Zikri Hasanbasri1, Shasha Qiu2, Guodong Rao1
1Department of Chemistry, University of California Davis, 1 Shields Ave, Davis, CA, USA.
Abstract:
Pulse Electron Paramagnetic Resonance (EPR) spectroscopy provides powerful tools for examining species with unpaired electrons, such as organic radicals and metal ions, in a wide variety of interesting systems. However, the lack of high power pulse amplifiers above approximately 100 GHz has limited its applicability at very high frequencies and magnetic fields. Here we describe the use of a new 10 W high frequency traveling wave vacuum tube amplifier employed in a pulse EPR spectrometer operating over a wide frequency bandwidth centered at 263 GHz. Very high frequency pulse EPR is of particular utility for studying spin S > 1/2 species, given that large broadening effects of "zero-field splitting" interactions often dominate EPR spectra obtained at low frequency. Improvements obtained at 263 GHz are illustrated for a series of high spin (S=5/2) Mn(II) complexes starting with Mn(II) impurities in a diamagnetic host up though Mn(II) bound in metal sequestering proteins. The instrument has sufficient mm-wave power to obtain high signal-to-noise electron spin echoes without a resonator, which offers a number of advantages as described herein.
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