High-field 285 GHz electron paramagnetic resonance study of indigenous radicals of humic acids
Related Experiment Video
Updated: Jul 10, 2026

Exploring the Radical Nature of a Carbon Surface by Electron Paramagnetic Resonance and a Calibrated Gas Flow
Published on: April 24, 2014
Konstantinos C Christoforidis1, Sun Un, Yiannis Deligiannakis
1Laboratory of Physical Chemistry, Department of Environmental and Natural Resources Management, University of Ioannina, Seferi 2, 30100 Agrinio, Greece.
Abstract:
Humic substances, the largest source of carbon on Earth, contain indigenous stable free radicals that are involved in important biogeochemical environmental processes occurring in soil and water systems. Here, we present the first high-magnetic-field 285GHz electron paramagnetic resonance spectra for humic acids from various geographical origins. All humic acids irrespective of their origin contain two limiting types of indigenous stable radicals, types I and II, with distinct electronic structure. Type I, which prevails at acidic pH 5, is characterized by a g tensor with principal values gIx = 2.0032, gIy = 2.0032, and gIz = 2.0023. Type II, which prevails at alkaline pH 12, is characterized by gIIx = 2.0057, gIIy = 2.0055, and gIIz = 2.0023. The two limiting types are correlated in a unified reversible manner with pH, irrespective of the geographic origin of the HA. Both types of radical centers are consistent with pi-type radicals. They persist not only in liquid solutions but also in humic acid powders.
More Related Videos
08:01Rapid Scan Electron Paramagnetic Resonance Opens New Avenues for Imaging Physiologically Important Parameters In Vivo
Published on: September 26, 2016
08:22Measurement of Ultrafast Vibrational Coherences in Polyatomic Radical Cations with Strong-Field Adiabatic Ionization
Published on: August 6, 2018
Related Concept Videos
Electron Paramagnetic Resonance (EPR) Spectroscopy: Organic Radicals
π Electron Effects on Chemical Shift: Overview
Radicals: Electronic Structure and Geometry
Accordingly, the structure of a trivalent radical lies between the geometries of carbocations and carbanions. An sp2-hybridized carbocation is trigonal planar, while an sp3-hybridized carbanion is trigonal pyramidal. Here, the difference in geometry is...
Other Nuclides: 31P, 19F, 15N NMR
While fluorine-19 and phosphorous-31 have high natural abundances (100%) and positive gyromagnetic ratios, nitrogen-15 has a low natural abundance and a negative gyromagnetic ratio. However, nitrogen-15 is still preferred over nitrogen-14 (which has a high...
Radical Reactivity: Steric Effects
Along with electronic factors, steric factors also account...
2D NMR: Heteronuclear Single-Quantum Correlation Spectroscopy (HSQC)