The chiral configuration of the title ligand, δ-L1, has been established by the X-ray crystal structure determination of its cobalt complex [Co(δ-L1)][BF4]2·0.5H2O. The compound crystallises in the orthorhombic space group Fddd, with a= 31.424(6), b= 24.633(5), c= 22.223(5)Å, and Z= 16. Least-squares refinement gave R= 0.080 for 1 695 observed reflections. The cobalt atom is low-spin and octahedrally co-ordinated by the macrocycle which adopts meridional configurations for the P(CH2)3S(CH2)3P moieties. The stereochemistry of some cobalt(II) and nickel(II) complexes of δ-L1 with 1 : 1, 2 : 1, and 3 : 2 metal-to-ligand ratios is discussed.
Ciampolini, M., Nardi, N., Orioli, P.L., Mangani, S., Zanobini, F. (1985). Macrocyclic Polyphosphane Ligands - Cobalt(ii) and Nickel(ii) Complexes of 5rs,8rs,16rs,19rs-tetraphenyl-5,8,16,19-tetraphospha-1,12-dithiacyclodoc Osane (delta-l1) and the Crystal-structure of [co(delta-l1)][bf4]2.0.5h2o. JOURNAL OF THE CHEMICAL SOCIETY DALTON TRANSACTIONS, 6, 1179-1182 [10.1039/dt9850001179].
Macrocyclic Polyphosphane Ligands - Cobalt(ii) and Nickel(ii) Complexes of 5rs,8rs,16rs,19rs-tetraphenyl-5,8,16,19-tetraphospha-1,12-dithiacyclodoc Osane (delta-l1) and the Crystal-structure of [co(delta-l1)][bf4]2.0.5h2o
Mangani, Stefano;Zanobini, F.
1985-01-01
Abstract
The chiral configuration of the title ligand, δ-L1, has been established by the X-ray crystal structure determination of its cobalt complex [Co(δ-L1)][BF4]2·0.5H2O. The compound crystallises in the orthorhombic space group Fddd, with a= 31.424(6), b= 24.633(5), c= 22.223(5)Å, and Z= 16. Least-squares refinement gave R= 0.080 for 1 695 observed reflections. The cobalt atom is low-spin and octahedrally co-ordinated by the macrocycle which adopts meridional configurations for the P(CH2)3S(CH2)3P moieties. The stereochemistry of some cobalt(II) and nickel(II) complexes of δ-L1 with 1 : 1, 2 : 1, and 3 : 2 metal-to-ligand ratios is discussed.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
https://hdl.handle.net/11365/31707
Attenzione
Attenzione! I dati visualizzati non sono stati sottoposti a validazione da parte dell'ateneo