Litcius/Paper detail

Construction of Ideal One-Dimensional Spin Chains by Topochemical Dehydration/Rehydration Route

Yanhong Wang, Peng Fu, Hiroshi Takatsu, Cédric Tassel, Naoaki Hayashi, Jiaojiao Cao, Thierry Bataille, Hyun‐Joo Koo, Zhongwen Ouyang, Myung‐Hwan Whangbo, Hiroshi Kageyama, Hongcheng Lu

2024Journal of the American Chemical Society10 citationsDOI

Abstract

One-dimensional (1D) Heisenberg antiferromagnets are of great interest due to their intriguing quantum phenomena. However, the experimental realization of such systems with large spin S remains challenging because even weak interchain interactions induce long-range ordering. In this study, we present an ideal 1D S = 5/2 spin chain antiferromagnet achieved through a multistep topochemical route involving dehydration and rehydration. By desorbing three water molecules from (2,2′-bpy)FeF 3 (H 2 O)·2H 2 O (2,2′-bpy = 2,2′-bipyridyl) at 150 °C and then intercalating two water molecules at room temperature (giving (2,2′-bpy)FeF 3 ·2H 2 O 1 ), the initially isolated FeF 3 ON 2 octahedra combine to form corner-sharing FeF 4 N 2 octahedral chains, which are effectively separated by organic and added water molecules. Mössbauer spectroscopy reveals significant dynamical fluctuations down to 2.7 K, despite the presence of strong intrachain interactions. Moreover, results from electron spin resonance (ESR) and heat capacity measurements indicate the absence of long-range order down to 0.5 K. This controlled topochemical dehydration/rehydration approach is further extended to (2,2′-bpy)CrF 3 ·2H 2 O with S = 3/2 1D chains, thus opening the possibility of obtaining other low-dimensional spin lattices.

Topics & Concepts

ChemistryOctahedronAntiferromagnetismElectron paramagnetic resonanceDehydrationMoleculeSpin (aerodynamics)CrystallographyAtmospheric temperature rangeChemical physicsCondensed matter physicsNuclear magnetic resonanceCrystal structureThermodynamicsOrganic chemistryPhysicsBiochemistryPhysics of Superconductivity and MagnetismAdvanced Condensed Matter PhysicsMagnetism in coordination complexes