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77953872842
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Syntheses: The ligand of HL2 was synthesized readily by the procedure reported in the literature [35,36, All chemicals were commercially available and used as received without further purification. The compound was synthesized by the following method: Zn(NO3)2·6H2O (0.089 g, 0.30 mmol, HL2 (0.033 g, 0.10 mmol, 1,4-H2bdc (0.050 g, 0.30 mmol) and NaOH (0.24 g, 0.60 mmol) in H2O (14 mL) was sealed in a 25 mL Teflon-lined stainless steel container, which was heated at 150 °C for 3 days and then cooled down to room temperature at a rate of 10 °C h-1. Colorless crystals of 1 were collected and washed with distilled water and dried in air to give the product; yield, 45.4, based on ZnII salts, Elemental analyses calcd, ) for C43H28N2O16Zn3 1024.78, C, 50.39; H, 2.76; N, 2.73. Found C, 50.41; H, 2.73; N, 2.75
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-1): 2920 (w), 2856 (w), 1709 (m), 1693 (w), 1677 (m), 1645 (m), 1616 (s), 1510 (s), 1428 (s), 1386 (s), 1275 (m), 1220 (m), 1023 (w), 814 (m), 813 (m), and 747 (s).
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38
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77953870640
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Crystal data for compound 1 C43H28N2O16Zn3: monoclinic, space group P21/c, a, 13.869(2) Å, b, 11.316(3) Å, c, 29.256(2) Å, α, 90o, β, 103.035(4)o, γ, 90°, V, 4473.2(14) Å3, Z, 4, Dc, 1.522 mg/m3, μ, 1.668 mm-1, 23295 reflections measured, 8433 unique, R(int, 0.0343) which were used in all calculations. R1, 0.0514 (I> 2σ (I, wR2, 0.1621 (all data) and S, 1.038. Data were collected on a Bruker ApexII CCD diffractometer with graphite-monochromated Mo Kα radiation (λ, 0.71073 Å, The structure was solved with direct methods and refined with full-matrix least-squares (SHELX-97, Selected bond lengths (Å) and angles (°) for compound 1 are listed in Table S1, Supporting information
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2 = 0.1621 (all data) and S = 1.038. Data were collected on a Bruker ApexII CCD diffractometer with graphite-monochromated Mo Kα radiation (λ = 0.71073 Å). The structure was solved with direct methods and refined with full-matrix least-squares (SHELX-97). Selected bond lengths (Å) and angles (°) for compound 1 are listed in Table S1, Supporting information.
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