Synthesis and characterization of a N-salicylaldimine ligand and its vanadium(V) complex

The reduction of 2-nitro-1,3-di(pyridin-2-yl)-1,3-di(tert -butyldimethylsilyloxy)propane 1 with sodium borohydride affords 2-amino-1,3-di(pyridin-2-yl)-1,3-di(tert-butyldimethylsilyloxy)propane 2 which was subsequently reacted with salicyl aldehyde yielding rac-((2,2,3,3,9,9,10,10-octamethyl-5,7-di(pyridin-2-yl)-4,8-dioxa-3,9-disilaundecan-6-ylimino)methyl)phenol (Proligand 3 = HL(SiMe2tBu)2), with excellent yield. Reaction of 3 with vanadyl acetylacetonate followed by aerial oxidation diastereoselectively led to the octahedral coordinated vanadium(V) complex 4([VO(OMe)L(SiMe2t Bu)]). Compound 3 together with vanadyl acetylacetonate as well as with molybdenyl acetylacetonate shows catalytic activity in the sulfoxidation of (methylsulfanyl)benzene I, which was followed by NMR spectroscopy. The vanadium complex 4 was also able to catalyze the sulfoxidation but was considerably slower. All three tested catalytic systems lead to almost quantitative formation of the sulfoxide with only minor formation of the respective sulfone.

A tetradentate Schiff-base ligand HL(SiMe2tBu)2) was prepared, which formed the vanadium(V) complex [VO(OMe)L(SiMe2tBu)] upon reaction with vanadyl acetylacetonate. NMR investigations together with X-ray diffraction results show that the complex is formed diastereospecifically. The complex is able to act as a catalyst in the sulfoxidation of (methylsulfanyl)benzene.Figure optionsDownload as PowerPoint slide