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Nature Communications· 2026Q1

Very high frequency (263 GHz) pulse EPR spectroscopy of high spin transition metal centers

Zikri Hasanbasri, Shasha Qiu, Guodong Rao, Amanda Caceres et al.

Short summary

A new 263 GHz pulse EPR spectrometer, powered by a 10 W traveling wave tube amplifier, enables high signal-to-noise measurements of high spin (S > 1/2) metal centers without a resonator.

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Key points

  • A new pulse EPR spectrometer operates at 263 GHz, significantly higher than previous limitations around 100 GHz.
  • The spectrometer utilizes a 10 W high frequency traveling wave vacuum tube amplifier.
  • It enables high signal-to-noise electron spin echoes without requiring a resonator.
  • The instrument is shown to be effective for studying high spin (S=5/2) Mn(II) complexes, including those in proteins.

AI-generated from the title and abstract; the full text is not read.

Abstract

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.

The authors' abstract, as published at the source. Nature Communications, 2026 · DOI ↗

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BiophysicsBiochemistry, Genetics and Molecular Biology