Five-membered heterocyclic 1,2,4-diazaphospholide ligands with lone pair electrons,? electronics,aromaticity,and low coordination of phosphorus played an important role in the preparation of organometallic complexes.With the 1,2,4-diazaphospholide anions,a few of vanadium and rhodium complexes with this type of the ligand were synthesize,including low-valent vanadium species.All of complexes have been fully characterized by X-ray single crystal diffraction,NMR,EPR,magnetic susceptibility,and IR:1.The reaction of potassium 3,5-disubstituted-1,2,4-diazaphospholide and vanadium trichloride tetrahydrofuran in a ratio of 3:1,2:1,and 1:1 gave complexes [?THF?V?3,5-tBu2dp?3],[Cl?THF?2V?3,5-tBu2dp?2],and [Cl2?THF?2V?3,5-tBu2dp?],respectively.2.The reaction of potassium 3,5-di-phenyl-1,2,4-diazaphospholide and vanadium trichloride tetrahydrofuran in a ratio of 3:1,2:1,and 1:1 gave complexes [?THF?V?3,5-Ph2dp?3],[Cl?THF?2V?3,5-Ph 2dp?2],and [Cl2?THF?2V?3,5-Ph2dp?],respectively.3.The reduction of [Cl2?THF?2V?3,5-tBu2dp?] and [Cl2?THF?2V?3,5-Ph2dp?] with C8 K gave two low-valent vanadium complexes [?THF?2V?3,5-t Bu2dp?2] and [Cl?THF?3V2?3,5-Ph2dp?3],respectively.4.The reaction of [Cp*RhCl2] and potassium 3,5-di-phenyl-1,2,4-diazaphospholide complex gave a trimeric complex [Cp*Rh?3,5-Ph2dp?]3. |