Ag<sup>I</sup>/V<sup>V</sup> Heterobimetallic Frameworks Generated from Novel-Type {Ag<sub>2</sub>(VO<sub>2</sub>F<sub>2</sub>)<sub>2</sub>(triazole)<sub>4</sub>} Secondary Building Blocks: A New Aspect in the Design of SVOF Hybrids
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A series of new silver(I)-containing MOFs [Ag2(tr2ad)2](ClO4)2 (1), [Ag2(VO2F2)2(tr2ad)2]·H2O (2), [Ag2(VO2F2)2(tr2eth)2(H2O)2] (3), and [Ag2(VO2F2)2(tr2cy)2]·4H2O (4) supported by 4-substituted bifunctional 1,2,4-triazole ligands (tr2ad = 1,3-bis(1,2,4-triazol-4-yl)adamantane, tr2eth = 1,2-bis(1,2,4-triazol-4-yl)ethane, tr2cy = trans-1,4-bis(1,2,4-triazol-4-yl)cyclohexane) were hydrothermally synthesized and structurally characterized. In these complexes, the triazole heterocycle as an N1,N2-bridge links either two adjacent Ag–Ag or Ag–V centers at short distances forming polynuclear clusters. The crystal structure of compound 1 is based on cationic {Ag2(tr)4}2+ fragments connected in a 2D rhombohedral grid network with (4,4) topology. The neighboring layers are tightly packed into a 3D array by means of argentophilic interactions (Ag···Ag 3.28 Å). Bridging between different metal atoms through the triazole groups assists formation of heterobimetallic AgI/VV secondary building blocks in a linear V–Ag–Ag–V sequence that is observed in complexes 2–4. These unprecedented tetranuclear {Ag2(VO2F2)2(tr)4} units (the intermetal Ag–Ag and Ag–V distances are 4.24–4.36 and 3.74–3.81 Å, respectively), in which vanadium(V) oxofluoride units possess distorted trigonal bipyramidal environment {VO2F2N}¯, are incorporated into 1D ribbon (2) or 2D square nets (3, 4) using bitopic μ4-triazole ligands. The valence bond calculation for vanadium atoms shows +V oxidation state in the corresponding compounds. Thermal stability and photoluminescence properties were studied for all reported coordination polymers.
