A Near-Ideal Molecule-Based Haldane Spin-Chain
Robert C. Williams, William J. A. Blackmore, Samuel P. M. Curley,, Martin R. Lees, Serena M. Birnbaum, John Singleton, Benjamin M. Huddart,, Thomas J. Hicken, Tom Lancaster, Stephen J. Blundell, Fan Xiao, Andrew, Ozarowski, Francis L. Pratt, David J. Voneshen, Zurab Guguchia

TL;DR
This study reports the synthesis and characterization of a molecule-based NiI2 complex that realizes a near-ideal S=1 Haldane spin chain with highly isotropic magnetic properties and accessible critical fields for phase exploration.
Contribution
It presents the first direct measurement of I–I magnetic coupling in a molecular chain, achieving a near-ideal Haldane system with minimal anisotropy and high magnetic isolation.
Findings
Measured I–I magnetic coupling directly for the first time.
Achieved a highly isotropic Haldane chain with D/J = -0.07.
Identified critical fields enabling exploration of the Haldane phase.
Abstract
The molecular coordination complex NiI(3,5-lut) [where (3,5-lut) (3,5-lutidine) (CHN)] has been synthesized and characterized by several techniques including synchrotron X-ray diffraction, ESR, SQUID magnetometry, pulsed-field magnetization, inelastic neutron scattering and muon spin relaxation. Templated by the configuration of 3,5-lut ligands the molecules pack in-registry with the Ni--II--Ni chains aligned along the --axis. This arrangement leads to through-space II magnetic coupling which is directly measured for the first time in this work. The net result is a near-ideal realization of the Haldane chain with and energy gaps of , split by the easy-axis single-ion anisotropy . The ratio affords one of the most isotropic…
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