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Updated: Jul 2, 2026

Synthesis of Single-Crystalline Core-Shell Metal-Organic Frameworks
Published on: February 10, 2023
Hydrothermal synthesis of vanadium oxyfluoride chains incorporating covalently bound copper coordination complexes
Thushitha Mahenthirarajah1, Yang Li, Philip Lightfoot
1EaStChem, School of Chemistry, University of St. Andrews, St. Andrews, Fife, KY16 9ST, United Kingdom.
Abstract:
An exploration of the hydrothermal synthesis of vanadium oxyfluorides in the presence of copper-amine coordination complexes has produced six new compounds exhibiting novel one-dimensional structural features. [C 2H 8N][Cu(C 5H 5N) 4][V 2O 2F 7] incorporates dimeric vanadium(IV) oxyfluoride units (in this case, face-sharing V-centered octahedra) into a compound of this type for the first time; this composition has been prepared in two polymorphs, 1 and 2, which differ in chain configuration and orientation, mediated by H bonding of the uncoordinated dimethylammonium cation. A differing dimeric vanadium(IV) oxyfluoride anion (based on edge-sharing V-centered octahedra) occurs in [C 3H 5N 2] 2[Cu(C 3H 4N 2) 4][V 2O 2F 8], 4, which incorporates imidazole in two structural roles: as both a ligand and template. [Cu 2F 2(C 10H 10N 3) 2][V 2O 7], 5, and [Cu(C 5H 5N) 2(C 2H 8N 2)][(VO 3) 2], 6, both contain V (5+) in tetrahedral coordination, in dimers in the former and infinite chains in the latter. In the case of 6, the copper moieties act as "decoration" rather than as linkers to the vanadium oxide sublattice.

