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- May 2012 (1)
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Single-crystal X-ray diffraction analyses were performed using a Bruker APEXII CCD
diffractometer mounted at the window of a Bruker FR591 rotating anode (MoKα = 0.71073 Å) and equipped with an
Oxford Cryosystems cryostream device. Data were processed using the Collect package and unit cell parameters
were refined against all data. An empirical absorption correction was carried out using SADABS . The structures
were solved by direct methods using SHELXS-97 and refined on Fo2 by full-matrix
least-squares refinements using SHELXL-97. All non-hydrogen atoms were refined with anisotropic displacement
parameters. All hydrogen atoms were added at calculated positions and refined using a riding model with
isotropic displacement parameters based on the equivalent isotropic displacement parameter (Ueq) of the parent
atom. Figures were produced using OLEX2