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The complex was obtained by mixing the ligand (1.17 mg, 3.38 μmol. 1 equiv) with AgBF4 (2.55 mg, 13.08 μmol, 3.9 equiv) in CD 3CN (0.4 mL, which lead to complete dissolution of the ligand and to precipitation of the most part of the complex. 1H NMR (CD 3CN, 300 MHz, after filtration: δ, 8.84 (s, 2H; H G, 8.30 (ddd. 7, 0.9, 1.7, 4.9 Hz, 2H; HA, 7.90 (s, 2H; HF, 7.84 (ddd, J, 1.9, 7.2, 8.7 Hz, 2H; HC, 7.47 (d, 7, 8.7 Hz, 2H; HD, 7.07 (ddd, 7, 0.9, 4.9, 7.2 Hz, 2H; H B, 3.65 s. 6H; HF, Crystals suitable for crystallographic determinations were obtained by diffusion of Et2O into a solution of the complex in CH3CN. Crystallographic data: C22H24Ag2B2F8N 111, C18H18N8Ag2· 2CH3CN·2BF4
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