Isolation of the novel dirhodium(II/II) thiolate compound Rh(2)(eta(1)-C(6)H(5)S)(2)(mu-C(6)H(5)S)(2)(bpy)(2)

The reaction of the anticancer active compound [Rh(2)(mu-O(2)CCH(3))(2)(bpy)(2)(CH(3)CN)(2)][BF(4)](2) (1) (bpy = 2,2'-bipyridine) with NaC(6)H(5)S under anaerobic conditions yields Rh(2)(eta(1)-C(6)H(5)S)(2)(mu-C(6)H(5)S)(2)(bpy)(2).CH(3)OH (2), which was characterized by UV-visible, IR, and (1)H NMR spectroscopies as well as single-crystal X-ray crystallography. Compound 2 crystallizes as dark red platelets in the monoclinic space group C2/c with cell parameters a = 20.398(4) A, b = 11.861(2) A, c = 17.417(4) A, beta = 108.98 degrees, V = 3984.9(14) A(3), Z = 4. The main structural features are the presence of a [Rh(2)](4+) core with a Rh-Rh distance of 2.549(2) A bridged by two benzene thiolate ligands in a butterfly-type arrangement. The axial positions of the [Rh(2)](4+) core are occupied by two terminal benzene thiolates. Cyclic voltammetric studies of 2 reveal that the compound exhibits an irreversible oxidation at +0.046 V in CH(3)CN, which is in accord with the fact that the compound readily oxidizes in the presence of O(2). The fact that this unusual dirhodium(II/II) thiolate compound is formed under these conditions is an important first step in understanding the metabolism of dirhodium anticancer active compounds with thiol-containing peptides and proteins.     

Iodidomesityltellurium(II) iodidotrimesitylditellurium(II)(Te—Te)

In the title compound, C₉H₁₁ITe·C₂₇H₃₃ITe₂ or (Mes)TeI·(Mes₂Te)TeI(Mes) (Mes is mesityl or 2,4,6‐trimethylphenyl), a strong Te...I interaction of 3.3157 (9) Å links the Te atom of an iodidomesityltellurium(II) moiety, (Mes)TeI, and an I atom of the iodidotrimesitylditellurium(II) unit, (Mes₂Te)TeI(Mes). Further weak Te...I contacts of 4.0818 (9) Å give rise to one‐dimensional chains along the b axis in the crystal structure. An intramolecular C—H...π(arene) interaction is present in the (TeMes₂)TeI(Mes) moiety, with a C...Cg distance of 3.497 (9) Å and a C—H...Cg angle of 142° (where Cg is the centroid of a mesityl ring of the Mes₂Te moiety).     

Dinuclear [Co(II)(NCMe)5Co(II)(NCS)4] possessing octahedral and tetrahedral Co(II) sites

The structural and magnetic properties of dinuclear [Co(II)(NCMe)(5)Co(II)(NCS)(4)]·MeCN have been investigated. The structure consists of an octahedral Co(II)(NCMe)(5) center connected to a tetrahedral Co(II)(NCS)(4) center bridged by a μ(1,3)-NCS(-) ligand. The bridging NCS(-) weakly couples the pair of S = (3)/(2) Co(II) spin sites, as evidenced by the magnetic data being best fit by the Curie-Weiss expression with θ = -15.5 K.     

New heterometallic coordination polymers self-assembled from copper(II) nitrate and (diamine)Pt(II)(pyridinecarboxylates)(2)

One-dimensional (1-D), two-dimensional (2-D), and three-dimensional (3-D) coordination polymers were prepared by self-assembly of binary metal complex systems, copper(II) nitrate and (en)Pt(II)(nic)(2) or (dmpda)Pt(II)(isonic)(2) (en = ethylenediamine, dmpda = 2,2'-dimethyl-1,3-propanediamine, nic = nicotinate, and isonic = isonicotinate), in aqueous solutions. Equimolar reactions of copper(II) nitrate with (dmpda)Pt(II)(isonic)(2) and (en)Pt(II)(nic)(2) resulted in 1-D ([(dmpda)Pt(isonic)(2)Cu(OH(2))(3)](NO(3))(2))(n)() (1) and 2-D ([(en)Pt(nic)(2)Cu(OH(2))](NO(3))(2))(n) (2), respectively, but the reaction of (en)Pt(II)(nic)(2) with excess copper(II) nitrate gave 3-D ([((en)Pt(nic)(2))(3)Cu(5)(OH)(2)(OH(2))(6)](NO(3))(8))(n) (3). The local structure of crystal 1 has a mononuclear copper unit, 2 has a dinuclear copper unit with a Cu-Cu distance of 2.659(5) A, and 3 has a pentanuclear copper unit. The methyl groups of the dmpda ligand are located in the space between two isonicotinate ligands of 1, which is presumed to be an important factor to determine the final structure of the crystal formed by self-assembly. Magnetic behaviors of crystals 1-3 examined in the temperature range of 4-300 K appear to be governed by the local structures around the copper(II) ions and do not indicate any significant long-range magnetic exchange interactions along the polymeric chain.