ࡱ> )+( m bjbj,(,( *NBNBWVV<<<<<PPP8  PNx{{{,x~<{{{{{<<{<<{8u9X0N< {{{{{{N{{{{{{{{{l :   X-ray crystal structure analysis for klat810c. A data crystal was selected, mounted on plastic mesh with viscous oil, cooled to 200 K, and diffraction data were collected on a Bruker-AXS Smart Apex using Mo k-alpha radiation monochromated by graphite. Data were corrected for absorption using multiscan methods [APEX2. Bruker AXS Inc., Madison, Wisconsin, USA, 2007] The structure was solved using direct methods and refined using full matrix least squares based on F2 with atomic scattering factors contained in the SHELXTL program suite (Sheldrick, G. M. (2008). Acta Cryst. A64, 112-122.). Systematic absences, equivalent reflections, and unit cell parameters are consistent for R-3c and R3c. Solution in the centrosymmetric space group yielded chemically reasonable and computational results of refinement. The molecule is located on a three-fold axis of symmetry. All nonhydrogen atoms were refined with anisotropic displacement parameters. All hydrogen atoms were placed in calculated positions as idealized contributions. 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