The syntheses of cationic ruthenium(II) complexes [Ru(Me₂-bpy)(PPh₃)₂RRʹ][PF₆]x {Me₂-bpy = 4,4ʹ-dimethyl-2,2ʹ-bipyridine, (3) R = Cl, Rʹ = N≡CMe, x = 1, (4) R = Cl, Rʹ = N≡CPh, x = 1, (5) R = Rʹ = N≡CMe, x = 2} and [Ru(Me₂-bpy)(κ²-dppf)RRʹ][PF₆]x {dppf = 1,1ʹ-bis(diphenylphosphino)ferrocene, (6) R = Cl, Rʹ = N≡CMe, x = 1, (7) R = Cl, Rʹ = N≡CPh, x = 1, (8) R = Rʹ = N≡CMe, x = 2} are reported, together with their structural confirmation by NMR (31P, 1H) and IR spectroscopy and elemental analysis, and, in the case of trans-[Ru(Me₂-bpy)(PPh₃)₂(N≡CCH₃)Cl][PF₆] (3), by X-ray crystallography. Electronic absorption and emission spectra of the complexes reveal that all complexes except 4 and 6 are emissive in the range 370–400 nm with 8 exhibiting an emission in the blue. Cyclic voltammetry studies of 3–8 show reversible or quasi-reversible redox processes at ca. 1 V, assigned to the Ru(II/III) couple.
In the title compound, C(20)H(13)N(3)S, the partially saturated ring adopts a twisted half-boat conformation with the methyl-ene C atom closest to the amino-benzene ring lying 0.690 (6) Å out of the plane defined by the five remaining atoms. The dihydro-phenanthrene residue has a folded conformation [dihedral angle between the outer benzene rings = 26.27 (18)°]. The thio-phen-2-yl ring forms a dihedral angle of 63.76 (19)° with the benzene ring to which it is attached. In the crystal, inversion dimers linked by pairs of N-H⋯N hydrogen bonds generate R(2) (2)(12) loops. The dimers are linked into layers in the bc plane by weak C-H⋯π inter-actions. The thio-phen-2-yl ring is disordered over two essentially coplanar but opposite orientations in a 0.918 (4):0.082 (4) ratio.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
In the title mol-ecule, C(10)H(8)N(2)O, the five- and six-membered rings form a dihedral angle of 10.14 (9)°. The aldehyde group is almost coplanar with the pyrazole ring to which it is connected [O-C-C-C torsion angle = -179.35 (17)°]. In the crystal, inversion dimers are linked by four C-H⋯O inter-actions as the carbonyl O atom accepts two such bonds. The dimeric aggregates are linked into supra-molecular layers in the ac plane by C-H⋯π and π-π [ring centroid(pyrrole)⋯ring centroid(phen-yl) = 3.8058 (10) Å] inter-actions.