Single-Chain Magnet Based on Cobalt(II) Thiocyanate as XXZ Spin Chain.
Michał RamsAleksej JochimMichael BöhmeThomas LohmillerMagdalena CeglarskaMarek M RamsAlexander SchneggWinfried PlassChristian NätherPublished in: Chemistry (Weinheim an der Bergstrasse, Germany) (2020)
The cobalt(II) in [Co(NCS)2 (4-methoxypyridine)2 ]n are linked by pairs of thiocyanate anions into linear chains. In contrast to a previous structure determination, two crystallographically independent cobalt(II) centers have been found to be present. In the antiferromagnetic state, below the critical temperature (Tc =3.94 K) and critical field (Hc =290 Oe), slow relaxations of the ferromagnetic chains are observed. They originate mainly from defects in the magnetic structure, which has been elucidated by micromagnetic Monte Carlo simulations and ac measurements using pristine and defect samples. The energy barriers of the relaxations are Δτ1 =44.9(5) K and Δτ2 =26.0(7) K for long and short spin chains, respectively. The spin excitation energy, measured by using frequency-domain EPR spectroscopy, is 19.1 cm-1 and shifts 0.1 cm-1 due to the magnetic ordering. Ab initio calculations revealed easy-axis anisotropy for both CoII centers, and also an exchange anisotropy Jxx /Jzz of 0.21. The XXZ anisotropic Heisenberg model (solved by using the density renormalization matrix group technique) was used to reconcile the specific heat, susceptibility, and EPR data.
Keyphrases
- monte carlo
- density functional theory
- room temperature
- single molecule
- molecularly imprinted
- molecular dynamics
- reduced graphene oxide
- ionic liquid
- metal organic framework
- high resolution
- magnetic resonance imaging
- machine learning
- electronic health record
- heat stress
- computed tomography
- mass spectrometry
- deep learning
- artificial intelligence