Related Experiment Video
Updated: Feb 20, 2026

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
Published on: July 27, 2022
Hysteretic Two-Step Spin-Crossover Behavior in Two Two-Dimensional Hofmann-Type Coordination Polymers
Fu-Ling Liu1, Jun Tao1,2
1Department of Chemistry, College of Chemistry and Chemical Engineering, Xiamen University, Xiamen, 361005, Fujian, P. R. China.
Abstract:
The reaction of ferrous salts and square-planar tetracyanometallates [MII (CN)4 ]2- (M=Pd, Pt) with ligand 4-(1H-pyrazol-3-yl)pyridine (Hppy) resulted in the formation of two two-dimensional (2D) Hofmann-like coordination polymers (CPs) with the general formula of {FeII (Hppy)2 [MII (CN)4 ]}⋅H2 O (M=Pd for 1Pd , Pt for 1Pt ). The two CPs have been studied by variable-temperature single-crystal X-ray crystallography, differential scanning calorimetry, and magnetic measurements. Polymers 1Pd and 1Pt are isostructures, in which the FeII atoms are equatorially coordinated with [MII (CN)4 ]2- to form 2D undulating layers and axially coordinated with Hppy ligands. Both compounds undergo cooperative, complete spin crossover (SCO), with characteristic abrupt and remarkable two equal steps, featuring hysteresis widths of 14 K and 19 K (1Pd ) and 17 and 23 K (1Pt ) for the two steps. The SCO cooperativity may result from the hydrogen bonds and π⋅⋅⋅π interactions within and between such 2D layers, and the two-step SCO behavior is accompanied with phase transitions.
More Related Videos
Related Concept Videos
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
Woodward–Hoffmann Selection Rules and Microscopic Reversibility
Spin–Spin Coupling: One-Bond Coupling
[3,3] Sigmatropic Rearrangement of 1,5-Dienes: Cope Rearrangement
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the involved orbitals. The...
Valence Bond Theory

