Abstract

Tantalum-alkyne complexes with the general formula TaCl3(R1C⋮CR2)(dme) (1a, R1 = R2 = Et; 1b, R1 = R2 = n-C5H11; 1c, R1 = Ph, R2 = Me; 1d, R1 = R2 = Ph; DME = 1,2-dimethoxyethane) were synthesized by treatment of the corresponding alkynes with a low-valent tantalum derived by reduction of tantalum pentachloride with zinc powder in a mixed solvent of toluene and DME. The DME ligand can be replaced by 2 equiv of pyridine to afford the corresponding dipyridine complexes TaCl3(R1C⋮CR2)(py)2 (2a, R1 = R2 = Et; 2b, R1 = R2 = n-C5H11; 2c, R1 = Ph, R2 = Me; 2d, R1 = R2 = Ph). Additionally, the reaction of 1a with the bidentate nitrogen ligands bipyridine and N,N,N‘,N‘-tetramethyethylenediamine (= TMEDA) gave TaCl3(EtC⋮CEt)(bipy) (3) and TaCl3(EtC⋮CEt)(tmeda) (4), respectively. The η2- and 4e-coordination mode of an alkyne with a large contribution of a metalacyclopropene canonical structure was revealed by spectroscopic methods (NMR and IR) and crystallographic analyses of 1a, 1c, 2a, and 4. The reactivies of the...

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call