Abstract

We report on a comprehensive characterization of the newly synthesized Cu2+^{2+}-based molecular magnet [Cu(pz)2_2(2-HOpy)2_2](PF6_6)2_2 (CuPOF), where pz = C4_4H4_4N2_2 and 2-HOpy = C5_5H4_4NHO. From a comparison of theoretical modeling to results of bulk magnetometry, specific heat, μ+μ^+SR, ESR, and NMR spectroscopy, this material is determined as an excellent realization of the 2D square-lattice S=1/2S=1/2 antiferromagnetic Heisenberg model with a moderate intraplane nearest-neighbor exchange coupling of J/kB=6.80(5)J/k_\mathrm{B} = 6.80(5) K, and an extremely small interlayer interaction of about 1 mK. At zero field, the bulk magnetometry reveals a temperature-driven crossover of spin correlations from isotropic to XYXY type, caused by the presence of a weak intrinsic easy-plane anisotropy. A transition to long-range order, driven by the low-temperature XYXY anisotropy under the influence of the interlayer coupling, occurs at TN=1.38(2)T_\mathrm{N} = 1.38(2) K, as revealed by μ+μ^+SR. In applied magnetic fields, our 1^1H-NMR data reveal a strong increase of the magnetic anisotropy, manifested by a pronounced enhancement of the transition temperature to commensurate long-range order at TN=2.8T_\mathrm{N} =2.8 K and 7 T.

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