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The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
Published on: April 10, 2015
Ruthenium(II) carbonyl compounds with the 4'-chloro-2,2':6',2''-terpyridine ligand
Rajendhraprasad Tatikonda1, Matti Haukka1
1University of Jyväskylä, Department of Chemistry, PO Box 35, FI-40014 University of Jyväskylä, Finland.
Abstract:
Two ruthenium carbonyl complexes with the 4'-chloro-2,2':6',2''-terpyridine ligand (tpy-Cl, C15H10ClN3), i.e. [RuCl(tpy-Cl)(CO)2][RuCl3(CO)3] (I) [systematic name: cis-di-carbonyl-chlorido(4'-chloro-2,2':6',2''-terpyridine-κ3N)ruthenium(II) fac-tricarbonyltri-chlorido-ruthenate(II)], and [RuCl2(tpy-Cl)(CO)2] (II) [cis-dicarbonyl-trans-di-chlorido(4'-chloro-2,2':6',2''-terpyridine-κ2N1,N1')ruthenium(II)], were synthesized and characterized by single-crystal X-ray diffraction. The RuII atoms in both centrosymmetric structures (I) and (II) display similar, slightly distorted octa-hedral coordination spheres. The coordination sphere in the complex cation in compound (I) is defined by three N atoms of the tridentate tpy-Cl ligand, two carbonyl carbon atoms and one chlorido ligand; the charge is balanced by an octa-hedral [Ru(CO)3Cl3]- counter-anion. In the neutral compound (II), the tpy-Cl ligand coordinates to the metal only through two of its N atoms. The coordination sphere of the RuII atom is completed by two carbonyl and two chlorido ligands. In the crystal structures of both (I) and (II), weak C-H⋯Cl inter-actions are observed.
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