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67349089191
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note
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-1, single crystals] 1524mw, 1455m, 1391m, 1348m, 1283m, 1259ms, 1138ms, 1044w, 936vw, 671vw, 542w, 514m, 472m, 450w, 424w, 383mw, 363ms, 335s.
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Pintus, G.7
Serpe, A.8
Trogu, E.F.9
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16
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67349232126
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note
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2 = 0.1011. The data were collected on a Stoe Imaging Plate Diffraction System (IPDS) equipped with an Oxford Cryosystems cooler device. The crystal-to-detector distance was 70 mm, 161 exposures (3.5 min per exposure) were obtained with 0 < φ{symbol} < 225° and with the crystals rotated through 1.4° in φ{symbol}. Crystal decay was monitored by measuring a maximum of 200 reflections per image. Cell parameters were obtained from 8000 reflections taken from the data measurements between 2° and 26°. The structure was solved by using direct methods (Sir97 [21]) and later refined by full-matrix least squares methods on F2 (Shelxl97 [22]). The calculations were carried out with the WINGX [23] programs package running on a PC. An absorption correction based on the multiscan method [24] was applied to the data set. The hydrogen atoms were introduced at their ideal positions and all of their parameters were refined. The structural drawings were generated by using the programs ORTEP [25] and CAMERON [26]. The atomic scattering factors were taken from the International Tables for X-ray Crystallography [27].
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18
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36248929835
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Clark, S.J.8
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0033138216
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24
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0242560405
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28
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ORTEP-III, M.N. Burnett, C.K. Johnson, Report ORNL-6895, Oak Ridge National Laboratory, Oak Ridge, Tennessee, 1996.
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