Abstract
Enantiomerically pure palladium complexes of different compositions, binuclear palladacycle containing the (sp 3)C–Pd bond (I) and mononuclear coordination palladium compound (II), are synthesized and studied by X-ray diffraction analysis. In complex I, the cyclopalladated ligands are in the cis position (CIF file CCDC no. 1049805 (I)). In compound II, the ligands coordinated through the monodentate mode occupy the trans position (CIF file CCDC no. 1049806 (II)).
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Original Russian Text © O.A. Zalevskaya, Ya.A. Gur’eva, P.A. Slepukhin, A.V. Kuchin, 2015, published in Koordinatsionnaya Khimiya, 2015, Vol. 41, No. 8, pp. 496–500.
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Zalevskaya, O.A., Gur’eva, Y.A., Slepukhin, P.A. et al. cis-Di-µ-chlorobis{(1S,4S)-2-[benzylimino]-7,7-dimethylbicyclo[2.2.1]heptylmethyl-C,N}dipalladium(II) and trans-dichlorobis{(1S,4S)-2-[benzylimino]-1,7,7-trimethylbicyclo[2.2.1]heptane-N}palladium(II): Syntheses and structural studies. Russ J Coord Chem 41, 532–536 (2015). https://doi.org/10.1134/S1070328415080114
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DOI: https://doi.org/10.1134/S1070328415080114