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A Low-Spin Co II /Nitroxide Complex for Distance Measurements at Q-Band Frequencies.
- Source :
- Magnetochemistry; Apr2022, Vol. 8 Issue 4, pN.PAG-N.PAG, 14p
- Publication Year :
- 2022
-
Abstract
- Pulse dipolar electron paramagnetic resonance spectroscopy (PDS) is continuously furthering the understanding of chemical and biological assemblies through distance measurements in the nanometer range. New paramagnets and pulse sequences can provide structural insights not accessible through other techniques. In the pursuit of alternative spin centers for PDS, we synthesized a low-spin Co<superscript>II</superscript> complex bearing a nitroxide (NO) moiety, where both the Co<superscript>II</superscript> and NO have an electron spin S of 1/2. We measured Co<superscript>II</superscript>-NO distances with the well-established double electron–electron resonance (DEER aka PELDOR) experiment, as well as with the five- and six-pulse relaxation-induced dipolar modulation enhancement (RIDME) spectroscopies at Q-band frequencies (34 GHz). We first identified challenges related to the stability of the complex in solution via DEER and X-ray crystallography and showed that even in cases where complex disproportionation is unavoidable, Co<superscript>II</superscript>-NO PDS measurements are feasible and give good signal-to-noise (SNR) ratios. Specifically, DEER and five-pulse RIDME exhibited an SNR of ~100, and while the six-pulse RIDME exhibited compromised SNR, it helped us minimize unwanted signals from the RIDME traces. Last, we demonstrated RIDME at a 10 μM sample concentration. Our results demonstrate paramagnetic Co<superscript>II</superscript> to be a feasible spin center in medium magnetic fields with opportunities for PDS studies involving Co<superscript>II</superscript> ions. [ABSTRACT FROM AUTHOR]
Details
- Language :
- English
- ISSN :
- 23127481
- Volume :
- 8
- Issue :
- 4
- Database :
- Complementary Index
- Journal :
- Magnetochemistry
- Publication Type :
- Academic Journal
- Accession number :
- 156599724
- Full Text :
- https://doi.org/10.3390/magnetochemistry8040043