The new oxofluoride Cu7(TeO3)6F2 has been synthesized by hydrothermal synthesis. It crystallizes in the triclinic system, space group P1̅. The crystal structure constitutes a Cu鈥揙 framework with channels extending along [001] where the F鈥?/sup> ions and the stereochemically active lone-pairs on Te4+ are located. From magnetic susceptibility, specific heat, and Raman scattering measurements we find evidence that the magnetic degrees of freedom of the Cu鈥揙鈥揅u segments in Cu7(TeO3)6F2 lead to a mixed dimensionality with single Cu S = 1/2 moments weakly coupled to spin-chain fragments. Due to the weaker coupling of the single moments, strong fluctuations exist at elevated temperatures, and long-range magnetic ordering evolves at comparably low temperatures (TN = 15 K).
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