115090-08-9Relevant articles and documents
Five-Co-ordinate Aryl- and Alkyl-Ruthenium(III) Porphyrin Complexes, and Ruthenium-Carbon Bond Strengths
Ke, Mingzhe,Rettig, Steven J.,James, Brian R.,Dolphin, David
, p. 1110 - 1112 (1987)
The ruthenium(III) complex Ru(OEP)Ph has been isolated and characterized crystallographically; its formation by the thermal decomposition of Ru(OEP)Ph2 allows an estimation of a Ru-C(sp2) bond strength.
Synthesis and characterization of dihalogenoruthenium(IV)-, diphenylruthenium(IV)-, and phenylruthenium(III)-tetraphenylporphyrin complexes, including the crystal structure of Ru(TPP)Br2
Ke, Mingzhe,Sishta, Chand,James, Brian R.,Dolphin, David,Sparapany, John W.,Ibers, James A.
, p. 4766 - 4771 (2008/10/08)
The paramagnetic (S = 1) Ru(TPP)X2 complexes (X = halide) are made by treatment of [Ru(TPP)]2 with HBr, HCl, or I2 (TPP = the dianion of 5,10,15,20-tetraphenylporphyrin). The dibromo species (2) crystallizes in the tetragonal system, space group C4h5-I4/m, with a = 13.686 (9) ?, c = 9.711 (7) ?, and Z = 2. The structure has been refined on F2 to final R and Rw values of 0.050 and 0.080, respectively, for 72 variables and 1639 observations; the value of R(F) for the 1354 reflections having Fo2 ≥ 3σ(Fo2) is 0.034. The molecule has imposed symmetry 4/m. As a consequence, the porphyrin plane is strictly planar; the phenyl rings are perpendicular to this plane, as is the Ru-Br bond. The Ru-Br distance is 2.425 (2) ?, the shortest recorded for any Ru-Br bond. 1H NMR isotropic shift data are consistent with π-donation from the halide. With PhLi, 2 yields diamagnetic Ru(TPP)Ph2 (5), which can be thermally decomposed to Ru(TPP)Ph (6); kinetic data imply a stronger Ru-C bond in 5 compared to the corresponding octaethylporphyrin complex (by 2.6 kcal/mol). A light-induced O2 oxidation of 6 gives diamagnetic [Ru(TPP)Ph]2O.
