In homogeneous catalysis, the catalyst is in the same phase as the reactant. The number of collisions between reactants and catalyst is at a maximum.In a patent, 254-60-4, name is 1,8-Diazanaphthalene, introducing its new discovery. Recommanded Product: 1,8-Diazanaphthalene
A series of new iridium(III) complexes containing pentamethylcyclopentadienyl (Cp* = eta5-C5Me5) and 1,8-naphthyridine (napy) have been prepared. X-ray crystallography revealed that napy acted as a monodentate, a didentate chelating, and a bridging ligand in complexes of [Cp*IrCl2(napy)] (1), [Cp*IrCl(napy)]PF6 (2), and [(Cp*IrCl)2(H)(napy)]PF6 (4), respectively. The crystal structure of [Cp*Ir(napy)2](PF6)2 (3) has also been determined; the dicationic complex bore both monodentate and chelating napy ligands. Dinuclear Cp*IrIII complex bridged by napy was only isolable if two IrIII centers were supported by a hydride (H-) bridge. In complexes 2 and 3, the four-membered chelate rings formed by napy exhibited a large steric strain; in the rings the N{single bond}Ir{single bond}N bond angles were only 60.5(2)-61.0(4) and the Ir{single bond}N{single bond}C angles were 94.7(8)-96.7(8). The bridging coordination of napy in complex 4 also afforded a large strain, i.e., the IrIII centers were displaced by 0.84(3) A? from the napy plane, due to the steric interaction between two Cp*IrCl moieties. The monodentate napy complex 1 in CDCl3 or CD2Cl2 at ambient temperature showed a rapid coordination-site exchange reaction, which gave two N sites of napy equivalent; at temperatures below -40 C, the 1H NMR spectra corresponded to the molecular structure of [Cp*IrCl2(napy-kappaN)]. The analogous diazido complex of [Cp*Ir(N3)2(napy)] (5) has also been prepared, and the crystal structure has been determined. In contrast to the dichloro complex 1, the diazido complex 5 exhibited a dissociation equilibrium of coordinated napy in solution.
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Reference£º
1,263-Naphthyridine – Wikipedia,
1,8-Naphthyridine | C8H6N257 – PubChem