X-ray structural analysis on single crystal of PdII complex was
carried out on a STOE IPDS-II diffractometer with graphite monochromated
Mo Ka radiation. The data were collected at a temperature
of 100(2) K to a maximum 2h value of 27.93 and in a
series of x scans in 1 oscillations with 150 s exposures. The crystal-
to-detector distance was 110 mm. The data were corrected for Lorentz and Polarizing effects. A numerical absorption correction
was applied [10,11]. The structure was solved by direct/heavyatom
Patterson [12] methods using SHELXL-97. All of the nonehydrogen
atoms were refined anisotropically. All of hydrogen
atoms were located in the difference Fourier map. The final cycle
of full-matrix least-squares refinement [13] on F2 was based on
2990 unique reflections