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note
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2] (2): C 31.67 H 1.65 O 26.38; Found: C 31.70 H 1.67 O 26.40%. The phase purity of 1 and 2 was confirmed by powder X-ray diffraction analysis, in which the experimental PXRD pattern is well consistent with that of the stimulated one (Fig. S1).
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19
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78649324999
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note
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Crystal data for 1: Mr = 640.47, a = 7.8208(16) Å, b = 24.616(5) Å, c = 10.961(2) Å, monoclinic, β = 104.91(3)° V = 2039.1(8) Å3, Z = 4, F(000) = 1208, GOF = 1.057, R1 = 0.0477, wR2 = 0.1146. Crystal data for 2: Mr = 606.32, a = 7.4341(4) Å, b = 13.3890(6) Å, c = 19.1036(9) Å, monoclinic, β = 98.813(1)° V = 1879.03(16) Å3, Z = 4, F(000) = 1136, GOF = 1.056, R1 = 0.0275, wR2 = 0.0685. Structural data for 1 and 2 were collected on a Bruker Smart APEX CCD diffractometer with graphite monochromatic Mo Kα radiation (λ = 0.71073 Å) at 298 K. The structures were solved by direct methods and refined using full-matrix least-squares technique with the SHELXTL version 6.1. Selected bond lengths and angles for 1 and 2 are presented in the Supplementary material (Table S1).
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