The electronic structures of dinuclear copper complexes of the general formula [GFA(CuX2)2], where X = Br or Cl and GFA denotes a redox-active bridging Guanidino-Functionalized Aromatic ligand, were analysed and compared. The diamagnetic complexes [GFA(CuBr2)2] can all be described as dinuclear CuI complexes with bridging GFA2+ dicationic ligand units exhibiting a [CuI-GFA2+-CuI] electronic str...

The luminescent complexes of triphenylphosphine and two interesting aminomethylphosphines: P(CH(2)N(CH(2)CH(2))(2)NCH(3))(3) and P(CH(2)N(CH(2)CH(2))(2)O)(3) with copper(I) iodide and 2,9-dimethyl-1,10-phenanthroline (dmp): [CuI(dmp)PPh(3)], [CuI(dmp)P(CH(2)N(CH(2)CH(2))(2)NCH(3))(3)] and [CuI(phen)P(CH(2)N(CH(2)CH(2))(2)O)(3)] are presented in this work. These complexes were characterized in s...

Reactions of scandium terminal imido complexes with CuI and [M(COD)Cl](2) (M = Rh, Ir) show two interesting reaction patterns, and the formed heterobimetallic complexes have intriguing structural features and show promising catalytic properties.

We have recently developed a series of arsenic ligands based on practical synthetic strategies. Herein, three kinds bidentate with rigid linkers were selected to construct dinuclear rhombic copper(I) iodide (CuI) complexes, whose structures analyzed by X-ray crystallography. They had sufficient solubility in organic solvents, and it was confirmed that their coordination forms kept the solutions...

The preparation of Pt(ii) complexes of the type trans-L2Pt(Ar)Cl, L2Pt(Ar)2, and L2Pt(Ar)(Ar') (L = PBu3, Ar = arylene) by CuI catalyzed reaction of cis-(PBu3)2PtCl2 with aryl-stannanes is reported. The reactions proceed at 25-60 °C in moderate to good yields. The reaction is demonstrated to occur with phenyl- and 2-thienyl-stannanes that include a variety of functionality, and all of the resul...

Bacteria possess cytosolic proteins (Csp3s) capable of binding large quantities of copper and preventing toxicity. Crystal structures of a Csp3 plus increasing amounts of CuI provide atomic-level information about how a storage protein loads with metal ions. Many more sites are occupied than CuI equiv added, with binding by twelve central sites dominating. These can form [Cu4 (S-Cys)4 ] interme...

Polynuclear copper(I) complexes with bridging bis(dicyclohexylphosphino)methane (dcpm) and iodide ligands, [Cu(2)(dcpm)(2)(CH(3)CN)(2)](BF(4))(2) (1), [Cu(2)(dcpm)(2)](BF(4))(2) (2), [(CuI)(3)(dcpm)(2)] (3), [(CuI)(4)(dcpm)(2)] (4), and [(CuI)(2)(dcpm)(2)] (5) were prepared and their structures determined by X-ray crystal analysis. The shortest Cu--Cu distance found in these complexes is 2.475(...

Two series of different Cu(I)-complexes of "click" derived mesoionic carbenes are reported. Halide complexes of the type (MIC)CuI (with MIC = 1,4-(2,6-diisopropyl)-phenyl-3-methyl-1,2,3-triazol-5-ylidene (for 1b), 1-benzyl-3-methyl-4-phenyl-1,2,3-triazol-5-ylidene (for 1c)) and cationic complexes of the general formula [Cu(MIC)2]X (with MIC =1,4-dimesityl-3-methyl-1,2,3-triazol-5-ylidene, X = C...

We report a combined experimental and theoretical investigation of MI(2)(-) (M = Cs, Cu, Ag, Au) to explore the chemical bonding in the group IA and IB diiodide complexes. Both photoelectron imaging and low-temperature photoelectron spectroscopy are applied to MI(2)(-) (M = Cs, Cu, Au), yielding vibrationally resolved spectra for CuI(2)(-) and AuI(2)(-) and accurate electron affinities, 4.52 ± ...

A new synthesis of 1,1,1-tris(pyrid-2-yl)ethane (L), and a survey of its coordination chemistry, are reported. The complexes [ML2](n+) (M(n+) = Fe(2+), Co(2+), Co(3+), Cu(2+) and Ag(+)), [PdCl2L] and [CuI(L)] have all been crystallographically characterised. Noteworthy results include an unusual square planar silver(i) complex [Ag(L)2]X (X(-) = NO3(-) and SbF6(-)); the oxidative fixation of aer...