R. V. Belzen, R. Klein, W. Smeets
1996
Citations
0
Influential Citations
22
Citations
Journal
Recueil des Travaux Chimiques des Pays-Bas
Abstract
The synthesis and characterization of substituted phenanthrene-9,10-quinone diimines of the type 9,10-bis(arylimino)-9,10-dihydrophenanthrene (aryl-BIP) is described. These rigid bisnitrogen ligands have been synthesized by a metal-mediated cyclodehydrogenation reaction from the aromatic open-chain diimine analogues derived from benzil. All aryl-BIP compounds adopt a Z,Z configuration in solution except for (o-iPr-phenyl)-BIP, which mainly exists in the E,Z form. All non-cyclic BIP compounds undergo a configurational change into the E,E isomer upon coordination to palladium. NDDO calculations on phenyl-BIP and its palladium dichloride complex have revealed that the energy of the LUMO is very much dependent on the puckering of the phenanthrene backbone and is in all cases lower than, for instance, that of the aromatic diimine of acenaphthene-1,2-quinone or open-chain diimines. The structures of phenyl-BIP and PdCl2-(phenyl-BIP) in the solid state have been determined by X-ray diffraction. Phenyl-BIP is triclinic, space group P, a = 12.392(1), b = 12.478(1), c = 14.633(2) A, α = 109.36(1), β = 91.57(1), γ = 115.82(1)°, Z = 4, final R = 0.0556 for 4494 reflections with I > 2.5σ(I). PdCl2-(phenyl-BIP) is monoclinic, space group P21/c, a = 20.5148(9), b = 10.6756(9), c = 23.2007(16) A, β = 105.13(1)°, Z = 4, final R = 0.0701 for 2569 reflections with I > 2.5σ(I).