Direct Ag−Pt2Interactions in Pentafluorophenyl A-Frame Complexes Containing Halide or OH-and Bis(diphenylphosphino)methane (dppm) as Bridging Ligands. Crystal Structures of [(C6F5)2Pt(μ-OH)(μ-dppm){Ag(PPh3)}Pt(C6F5)2]·C7H8and [(C6F5)2Pt(μ-SC4H8)(μ-dppm)Pt(C6F5)2]·1/2C6H14

1996 ◽  
Vol 35 (26) ◽  
pp. 7867-7872 ◽  
Author(s):  
José María Casas ◽  
Larry R. Falvello ◽  
Juan Forniés ◽  
Antonio Martín
2021 ◽  
Author(s):  
Jianwei Wang ◽  
Xinhua Li ◽  
Caixia Yuan ◽  
Feng Su ◽  
Yanbo Wu ◽  
...  

A series of new dinuclear platinum(II) complexes with general formula [Pt2(μ-HL)4] (1–4), where H2L is 4-[(5-chloro-2-hydroxy-benzylidene)-amino)]-3-R-1,2,4-triazole-5-thione: R = H (1), methyl (2), ethyl (3) and propyl (4), have been synthesized...


1995 ◽  
Vol 50 (5) ◽  
pp. 828-832 ◽  
Author(s):  
Joachim Pickardt ◽  
Isabella Hoffmeister

Abstract Crystals of both complexes were obtained by evaporation of the ethanol solvent. The crystals of [{CuCl(C10N4H24)}2][CdCl4] are tetragonal, space group I4̄2d, Z = 4, a = b = 1784.1(11), c = 1101.1(8) pm. Each copper atom is bonded to one cyclam ligand and two chlorine atoms which are acting as bridging ligands and connect the copper atoms to chains of distorted octahedra. Distorted tetrahedra of CdCl4 are situated in cavities between these chains. The crystals of [Cu(C10N4H24)][CdCl3(H2O)2]Cl are monoclinic (b), space group C2/c, Z = 4, a = 1581.9(8), b = 1323.3(7), c = 924.0(5) pm, β = 94.31(5)°. Cadmium is coordinated to four chlorine atoms and two water molecules, while all of the chlorine atoms act as bridging ligands connecting every cadmium atom to two adjacent cadmium atoms and to two copper atoms which lie in plane with the N atoms.


2020 ◽  
Vol 76 (8) ◽  
pp. 1213-1221
Author(s):  
Elizabeth C. Manickas ◽  
Matthias Zeller ◽  
Curtis M. Zaleski

The syntheses and crystal structures for the compounds tetra-μ-aqua-tetrakis{2-[azanidylene(oxido)methyl]phenolato}tetrakis(μ2-3-hydroxybenzoato)dysprosium(III)tetramanganese(III)sodium(I) N,N-dimethylacetamide decasolvate, [DyMn4Na(C7H5O3)4(C7H4NO2)4(H2O)4]·10C4H9NO or [DyIIINa(4-OHben)4{12-MCMn(III)N(shi)-4}(H2O)4]·10DMA, 1, and tetra-μ-aqua-tetrakis{2-[azanidylene(oxido)methyl]phenolato}tetrakis(μ2-3-hydroxybenzoato)dysprosium(III)tetramanganese(III)sodium(I) N,N-dimethylformamide tetrasolvate, [DyMn4Na(C7H5O3)4(C7H4NO2)4(H2O)4]·4C3H7NO or [DyIIINa(3-OHben)4{12-MCMn(III)N(shi)-4}(H2O)4]·4DMF, 2, and where MC is metallacrown, shi3− is salicylhydroximate, 3-OHben is 3-hydroxybenzoate, DMA is N,N-dimethylacetamide, 4-OHben is 4-hydroxybenzoate, and DMF is N,N-dimethylformamide, are reported. For both 1 and 2, the macrocyclic metallacrown consists of an [MnIII—N—O] ring repeat unit, and the domed metallacrown captures two ions in the central cavity: a DyIII ion on the convex side of the metallacrown and an Na+ ion the concave side. The MnIII ions are six-coordinate with an elongated tetragonally distorted octahedral geometry. Both the DyIII and Na+ ions are eight-coordinate. The DyIII ions possess a square-antiprismatic geometry, while the Na+ ions have a distorted biaugmented trigonal–prismatic geometry. Four 3-hydroxybenzoate or 4-hydroxybenzoate ligands bridge each MnIII ion to the central DyIII ion. For 1, whole-molecule disorder is observed for the main molecule, excluding only the DyIII and Na+ ions, and the occupancy ratio refined to 0.8018 (14):0.1982 (14). Three DMA molecules were refined as disordered with two in general positions by an approximate 180° rotation and the third disordered twice by general disorder as well as by an exact 180° rotation about a twofold axis that bisects it. The occupancy ratios refined to 0.496 (8):0.504 (8), 0.608 (9):0.392 (9), and 2×0.275 (7):2×0.225 (7), respectively. For 2, segments of the metallacrown are disordered including the DyIII ion, one of the Mn ions, two of the Mn-bound 4-hydroxybenzoate ligands, the Mn-bridging salicylhydroximate ligand, and portions of the remaining three shi3− ligands. The occupancy ratio for the metallacrown disorder refined to 0.849 (9):0.151 (9). Two DMF solvent molecules are also disordered, each over two orientations. The disorder ratios refined to 0.64 (3):0.36 (3) and to 0.51 (2):0.49 (2), respectively. For 2, the crystal under investigation was refined as a non-merohedric twin by a 90° rotation around the real a axis [twin ratio 0.9182 (8):0.0818 (8)].


1990 ◽  
Vol 389 (3) ◽  
pp. 361-374 ◽  
Author(s):  
Kenneth I. Hardcastle ◽  
Tim McPhillips ◽  
Alejandro J. Arce ◽  
Ysaura De Sanctis ◽  
Antony J. Deeming ◽  
...  

1990 ◽  
Vol 43 (4) ◽  
pp. 643 ◽  
Author(s):  
NW Alcock ◽  
II Creaser ◽  
NJ Curtis ◽  
L Roecker ◽  
AM Sargeson ◽  
...  

A synthesis of [( tren )Co(μ-NH2,μ-OH)Co( tren )]4+(3)( tren = tris (2- aminoethyl )amine) is reported along with a series of derivatives: [( tren ) XCo (μ-NH2) CoX ( tren )]n+, where X = CF3SO3- (n = 3)(4), X = CH3CN (n = 5)(5), and [( tren )Co(μ-NH2,μ-CH3C(O)NH)Co( tren )]4+ (6). The substitution of (4) by CH3CN to yield (5) was studied in CH3CN at 20°C, k = 9.0×10-3 s-1, and the intramolecular hydrolysis of (5) to yield the bridging acetamide complex (6) was studied at various acid concentrations. The X-ray crystal structures were determined for (3b) (exafluorophosphate, dihydrate) and (6b) (dithionate, tetrahydrate ). Both crystals are monoclinic, respectively P21/n with a 11.082(2), b 10.402(2), c 15.611(2)Ǻ, β 99.13(2)°, Z 2, and C2/c with a 14.328(2), b 14.046(1), c 16.497(2)Ǻ, β 101.90(1)°, Z 4. For the salt of (3), 2389 data with 1 ≥ 2σ(I) were refined to R 0.070 ( Rw 0.066), and, for the salt of (6), 3087 data with I ≥ 3σ(I) were refined to R 0.041 ( Rw 0.056). Both ions lie on pseudo-symmetric sites involving disorder of the bridging ligands . The structures establish the binding mode of the acetamido ion and the orientation of the tren groups in the isolated complexes.


2003 ◽  
Vol 42 (8) ◽  
pp. 2545-2552 ◽  
Author(s):  
Sanjit Konar ◽  
Partha Sarathi Mukherjee ◽  
Michael G. B. Drew ◽  
Joan Ribas ◽  
Nirmalendu Ray Chaudhuri

2011 ◽  
Vol 17 (7) ◽  
pp. 2176-2188 ◽  
Author(s):  
Jesús Ferrando-Soria ◽  
Emilio Pardo ◽  
Rafael Ruiz-García ◽  
Joan Cano ◽  
Francisco Lloret ◽  
...  

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