In the title compound, [CoCl(C2H7N)(C3H10N2)2]Cl2, the Co(III) ion has a distorted octa-hedral coordination environment and is surrounded by four N atoms in the equatorial plane, with the other N and Cl atoms occupying the axial positions. The crystal packing is stabilized by N-H⋯Cl hydrogen bonds, forming a layered arrangement parallel to (1-10).

In the title mol-ecular salt, (C(11)H(10)N)[AuCl(4)], the Au(III) atom adopts an almost regular square-planar coordination geometry and the dihedral angle between the aromatic rings of the 3-phenyl-pyridinium cation is 23.1 (3)°. In the crystal, the ions inter-act by way of N-H⋯Cl and C-H⋯Cl hydrogen bonds.

The first anhydrous molecular complexes of uranium(III) chloride, soluble in polar aprotic solvents, are reported, including the structures of the dimeric [UCl3(py)4]2 and the trimetallic [UCl(py)4(μ-Cl)3U(py)2(μ-Cl)3UCl2(py)3].

Treatment of difluorobenzyldiphenylphosphine with the Ir(III) dimer [(dfppy)2Ir(mu-Cl)]2 gives (N,N)-trans-[Ir(dfppy)2(dfbdpH)Cl], followed by skeletal isomerization to form its (N,N)-cis analogue, and then the fully cyclometalated complex [Ir(dfppy)2(dfbdp)]; the last complex and its derivative are suitable for fabrication of true-blue phosphorescent OLEDs.

A cyclometalated iridium(III) complex containing a N∧C∧N-coordinating terdentate ligand [Ir(dpyx-N,C,N)Cl(μ-Cl)]2 was found to be a general and highly effective catalyst for the α-alkylation of ketones and N-alkylation of amines with alcohols. In the presence of catalyst (1 mol % Ir) and base (0.2-0.5 equiv), a variety of desirable products were obtained in good yields under an air atmosphere. ...

Four new complexes of the type [LCo ((DO)(DOH) pn) Cl] PF , where (DO) (DOH) pn = N , N '- propanediylbis (2, 3-butanedione2-imine3-oxirne)a nd L =morpholine (mrpln) (I), benzylamine (bzlan) (II), piperidine (pprdn)(III) and pyrrolidine (prldn) (IV) have been synthesized and characterized by elemental analyses and spectroscopic methods. Approximate values of the angular-overlap parameter, ?, ...

In the title salt, (C(20)H(26)N(2)O(2))[FeCl(4)]Cl·H(2)O, the Fe(III) atom exists in a tetra-hedral coordination environment. The cation, anions and water mol-ecules are linked by N-H⋯Cl, O-H⋯Cl and O-H⋯O hydrogen bonds into a layer network.

(Monooxooctaethylchlorinato)iron(III) chloride, (oxo-OEC)FeCl, 1, has been investigated by X-ray crystallography and by 1H NMR spectroscopy. Its bis(imidazole-d4) complex has been studied by multidimensional 1H NMR and EPR spectroscopies, and the results are compared to those for the bis(Im-d4) complex of (octaethylchlorinato)iron(III) chloride, (OEC)FeCl, 2. EPR and NMR results show that both ...

The title compound, [Co(C(18)H(18)N(2)O(4))Cl(H(2)O)]·H(2)O, contains a distorted octa-hedral cobalt(III) complex with a 6,6'-dimeth-oxy-2,2'-[ethane-1,2-diylbis(nitrilo-dimethyl-idyne)]diphenolate ligand, a chloride and an aqua ligand, and also a disordered water solvent mol-ecule (half-occupancy). The Co(III) ion is coordinated in an N(2)O(3)Cl manner. Weak O-H⋯O hydrogen bonds may help to st...

Dilute aqueous solutions of Rhodium (III) at the Cl~/Rh(III) ratios 4.86 and 10.7 have been X-ray examined. Octahedral R h ( H 2 0 ) ^ + and Rh(H 2 0) 3 Cl 3 complexes are the species which are consistent with the correlation functions and the structure functions. The average number of bonded chloride ions per Rhodium atom has been determined and the reliability of the structural information is...