Stereochemie der Metall-Metall-Bindung: Darstellung und Struktur von Co2(CO)4C5H5P(CH3)2 / Stereochemistry of the Metal-Metal Bond: Preparation and Structure of Co2(CO)4C5H5P(CH3)2

1978 ◽  
Vol 33 (5) ◽  
pp. 537-541 ◽  
Author(s):  
Egbert Keller ◽  
Heinrich Vahrenkamp

Abstract The title complex 4 was prepared from η-C3H5Co(CO)3 and η-C5H5(CO)Co-P(CH3)2H. It completes the series of PR2-and AsR2-bridged homodinuclear complexes C2(CO)7C5H5-As(CH3)2, Mn2(CO)6C5H5As(CH3)2, and Fe2(CO)5C5H5P(CH3)2. Its crystal structure analysis reveals the systematic variation of the ligand distribution along the series which depends only on the number of ligands present and not on given coordination geometries. The metal-metal bond length in 4 is mainly determined by the stereochemical require-ments of the bridging phosphido ligand.

1975 ◽  
Vol 30 (9-10) ◽  
pp. 814-815 ◽  
Author(s):  
Heinrich Vahrenkamp

The crystal structure of the title complex 1 shows that its metal-metal bond length is not determined by the radii of the metal or phosphorus atoms but by steric hindrance between vicinal carbonyl groups.


1992 ◽  
Vol 47 (6) ◽  
pp. 814-818 ◽  
Author(s):  
Karin Ruhlandt-Senge ◽  
Alfred Dirk Bacher ◽  
Gertraude Koellner ◽  
Birgit Siewert ◽  
Ulrich Müller

Reaction of VC14 with (Me3Si)2S in CH2C12 yields an insoluble product with the approximate composition VSC12. Its reaction with PPh4Cl in CH2Cl2 affords (PPh4)3[V2Cl9] · 7 CH2Cl2, whereas PPh4[VOCl4] is formed in the presence of oxygen. According to an X-ray crystal structure analysis, (PPh4)3[V2Cl9] · 7 CH2Cl2 contains [V2C19]3- ions having two face-sharing coordination octahedra but no significant metal-metal bonding (V-V distance 327.5 pm). Crystal data: a = 1386.4(7), b = 1405.6(7), c = 2710(2) pm, α = 95.800(5), β = 95.370(5), γ = 118.11(3)°, triclinic, Ρ 1̄, Ζ = 2; R = 0.066 for 8779 observed reflexions. PPh4[VOCl4] is isotypic with AsPh4[VOCl4] and contains tetragonal-pyramidal [VOCl4]- ions; tetragonal, P4/n, Z = 2, a = 1264.5(2), c = 772.0(2) pm; R = 0.050 for 654 observed reflexions.


1996 ◽  
Vol 51 (12) ◽  
pp. 1675-1678 ◽  
Author(s):  
Klaus Kopka ◽  
Rainer Mattes

The title complex was obtained by reaction of guanidinium dioxodipicolinatovanadate(V) and N-methyl-N-phenylhydrazine. According to the single crystal structure analysis the dinuclear anion [(μ-PhNNH)(μ-OCH3){(MePhNN(dipic)V)}2]- with sevenfold coordinated metal centers contains two types of hydrazido ligands. The ligand [MePhNN]2- is terminally bonded, and the VNN unit is linear with extensive electron delocalisation. The V-N and N-N bond lengths are 167.9(5) and 131.9(6) pm, respectively. The bonding of the bridging ligand is of the hitherto unknown μ-μ2:μ2 type, with V-N and N-N bond lengths of 202.5(5) and 136.5(5) pm, respectively. The V(N2)V moiety is not planar. The compound was also characterized by 1H and 51V NMR spectroscopy.


1986 ◽  
Vol 41 (11) ◽  
pp. 1431-1436 ◽  
Author(s):  
Max Herberhold ◽  
Heidemarie Kniesel ◽  
Ludwig Haumaier ◽  
Alfred Gieren ◽  
Catalina Ruiz-Péreza

Abstract The σ-ferrocenyl complex CpW (NO)2Fc (1) was prepared from CpW (NO)2Cl and ferrocenyl lithium, and oxidized by air in CH2Cl2 solution to give CpWO2Fc (2). An X-ray crystal structure analysis of 1 indicated the presence of two almost linear nitrosyl groups (with W -N -O angles of 173.0(9) and 175.4(7)°). The W -C (ferrocenyl) bond length is 2.164(10) Å.


Author(s):  
M. Bidya Sagar ◽  
K. Ravikumar ◽  
Y. S. Sadanandam

AbstractThe crystallographic characterization of the following three calcium channel antagonists is reported here: 2,6-dimethyl-3,5-dicarbamoyl-4-[2-nitro]-1,4-dihydropyridine (


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