Loading…
Properties of an organic model \(S=1\) Haldane chain system
We present the properties of a new organic \(S=1\) chain system \(m\)-NO\(_2\)PhBNO (abbreviated BoNO). In this biradical system two unpaired electrons from aminoxyl groups are strongly ferromagnetically coupled (\(|J_\text{FM}| \gtrsim 500\) K) which leads to the formation of an effective \(S=1\) s...
Saved in:
Published in: | arXiv.org 2024-10 |
---|---|
Main Authors: | , , , , , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | We present the properties of a new organic \(S=1\) chain system \(m\)-NO\(_2\)PhBNO (abbreviated BoNO). In this biradical system two unpaired electrons from aminoxyl groups are strongly ferromagnetically coupled (\(|J_\text{FM}| \gtrsim 500\) K) which leads to the formation of an effective \(S=1\) state for each molecule. The chains of BoNO diradicals propagate along the crystallographic \(a\) axis. Temperature dependence of the \(g\) factor and electron paramagnetic resonance (EPR) linewidth are consistent with a low-dimensional system with antiferromagnetic interactions. The EPR data further suggest that BoNO is the first known Haldane system with an almost isotropic \(g\) factor (\(2.0023 \pm 2 \unicode{x2030}\)). The magnetization measurements in magnetic fields up to \(40\) T and low-field susceptibility, together with \(^1\)H nuclear magnetic resonance (NMR) spectra, reveal a dominant intrachain antiferromagnetic exchange coupling of \(J_\text{1D} = (11.3\pm0.1)\) K, and attainable critical magnetic fields of \(\mu_0 H_\text{c1} \approx 2\) T and \(\mu_0 H_\text{c2} \approx 33\) T. These measurements therefore suggest that BoNO is a unique Haldane system with extremely small magnetic anisotropy. Present results are crucial for a future in-depth NMR study of the low-temperature Tomonaga-Luttinger liquid (TLL) and magnetic field-induced phases, which can be performed in the entire phase space. |
---|---|
ISSN: | 2331-8422 |