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max = 0.8970/0.7685). X-ray data collection was carried out using a Bruker APEX II diffractometer with a CCD area detector. There was no evidence of crystal decay during data collection. Semiempirical multi-scan absorption corrections were applied (SADABS), and the program SAINT was used for integration of the diffraction profiles. The structure was solved by direct methods and refined with the full-matrix least-squares technique using the SHELXS-97 and SHELXL-97 progranms. All nonhydrogen atoms were treated anisotropically. C-bound H atoms of the ligands were placed geometrically refined as riding atoms. The staring position of H attached to oxygen atom were located in differences Fourier synthesis and then fixed geometrically as riding atoms. CCDC-764132 contains the supplementary crystallographic data for this paper.
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