Monodentate ligands, molybdenum complexes

In seven-coordinate molybdenum peroxo complexes of the type Mo(0)(02)2L2, there is the problem of dissociation of the complex in the case of monodentate ligands like pyridine, HMPA, DMF or H2O. Bidentate hgands like 2,2 -bipyridine, on the other hand, tend to give insoluble complexes. A solution to this problem was presented by Thiel in 1997 and 1998 . His group utilized the Mo-diperoxo complex 160 bearing a pyrazolylpyridine ligand. 

Molybdenum trioxide, intercalation into, 12, 823 Molybdocenes, as anticancer agents, 1, 892 MOMNs, see Metal-organometallic coordination networks Monisocyanides, with silver(I) complexes, 2, 223 Monitoring methods, kinetic studies, 1, 513 Mono(acetylacetonate) complexes, with Ru and Os halfsandwich rf-arenes, 6, 523 tj2-Monoalkene monodentate ligands, with platinum divalent derivatives, 8, 617 tetravalent derivatives, 8, 625 theoretical studies, 8, 625 zerovalent derivatives, 8, 612... 

Few monomeric d4 bisalkyne complexes with only monodentate ligands in the coordination sphere have been reported. The only molybdenum(II) complex in this category is Mo(PhC=CR)2(CO)(NCMe)I2 (R = Ph, Me), which was included in a reaction scheme illustrating products accessible from cleavage of the iodide bridges in dimeric [Mo(PhC=CR)(/r-I)-(I)(CO)(CNMe)]2 reagents (51). Efforts to convert Mo(RC=CR)(CO)-L2X2 complexes to bisalkyne derivatives were not successful (46). 

Mononuclear Mov complexes with sterically hindered monodentate thiolato ligands are of interest as models for special molybdenum enzymes (the Mo oxidases). Here dimer formation via thiolato bridges and sulfide formation by C—S bond cleavage do not occur. Such a ligand is TIPTH. The complex [Mo(CO)2(TIPT)3) (14), with essentially trigonal prismatic coordination about Mo and trans CO groups in the axial sites, can be obtained.91... 

---