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Transition metal complexes with thiosemicarbazide-based ligands. LIII. [4-(2-Diphenylphosphino-α-ethoxybenzyl-κ<i>P</i>)-<i>S</i>-methyl-1-(4-oxidopent-3-en-4-ylidene-κ<i>O</i>)thiosemicarbazido-κ<sup>2</sup><i>N</i><sup>1</sup>,<i>N</i><sup>4</sup>]nickel(II)

Bojana M. DraškovićVinca Institute of Nuclear Sciences, Laboratory of Theoretical Physics and Condensed Matter Physics, PO Box 522, 11001 Belgrade, Serbia and MontenegroGoran A. BogdanovićVinča Institute of Nuclear Sciences, Laboratory of Theoretical Physics and Condensed Matter Physics, PO Box 522, 11001 Belgrade, Serbia and MontenegroVukadin M. LeovacDepartment of Chemistry, Faculty of Sciences, University of Novi Sad, Trg Dositeja Obradovića 3, 21000 Novi Sad, Serbia and MontenegroIlija BrčeskiFaculty of Chemistry, University of Belgrade, Studentski trg 16, 11000 Belgrade, Serbia and MontenegroDejan PoletiDepartment of General and Inorganic Chemistry, Faculty of Technology and Metallurgy, University of Belgrade, Karnegijeva 4, 11000 Belgrade, Serbia and Montenegro
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Abstract

The title compound, [Ni(C(28)H(30)N(3)O(2)PS)], crystallizes with two independent molecules in the asymmetric unit. The Ni(II) atoms are in significantly deformed square-planar environments formed by an ONNP donor set from a thiosemicarbazide-based tetradentate ligand. The Ni(II) atom and the ONN donor atoms are nearly coplanar, while the P atom deviates from their mean planes by 0.278 (4) and 0.202 (4) Angstrom for the two independent molecules. The P-containing chelate rings are remarkably non-planar, adopting a boat conformation, which is unusual for chelate rings in transition metal complexes with thiosemicarbazide-based tetradentate ligands. The orientation of the ethoxy group bonded to this chelate ring is caused by an intramolecular C-H...pi interaction with the opposing phenyl ring. There are no hydrogen bonds; instead, numerous intermolecular C-H...pi interactions dominate in the crystal packing.

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