Molybdenum complexes mono

Mono 0x0 molybdenum(V) complexes such as (NH 2 oOCl3 are quite common (see also Fig. 3b). 

The catalytic use of the mono-alkene molybdenum complex in converting H2C = CHSnR3 to H2C = CHCH2SnR3 has also been investigated.43 In this... 

Another procedure to access mono-oxo molybdenum(vi) complexes was established as shown in Figure 6.10. By reacting a five-coordinate bis(dithi-olene)mono-oxo molybdenum(vi) complex with carboxylate anions at low... 

Direct comparisons of the stability constants for formation of the dmpp complexes of molybdenum(VI) with those for uranium(VI) are not possible. The mono-ligand complexes have different stoichiometries, MoOaldmpp) versus U02(dmpp), while although log P2 is available for Mo02(dmpp)2 (175) the value of 40.2 refers to formation from Mo04 rather than from MoOg laq), and U02(dmpp)2 is too sparingly soluble for its formation constant to be determined (231). 

A large number of studies devoted to metal-sulfur centers are motivated by the occurrence of such arrangements at the active site of various metalloenzymes [1-13]. Mononuclear complexes with Mo=0 func-tion(s) and possessing sulfur ligands in their coordination sphere have been extensively investigated since they can be seen as models of the active site of enzymes such as nitrate- and DM SO reductases or sulfite- and xanthine oxidases [1-4]. On the other hand, a large variety of mono-, di-, and polynuclear Mo—S centers have been synthesized in order to produce functional models of the Mo-nitrogenase since the exact nature (mono-, di- or polynuclear) of the metal center, where N2 interacts within the iron-molybdenum cofactor (FeMo—co) of the enzyme is still unknown [4-8]. 

HIGH-VALENT MONO- -PENTAMETHYLCYCLO-PENTADIENYL)VANADIUM AND MOLYBDENUM COMPLEXES... 

A catalytic asymmetric oxidation of mono-, di-, and tri-substituted alkenes using a chiral bishydroxamic acid (BHA) complex of molybdenum catalyst in air at room temperature leads to good to excellent selectivity. It has been suggested that the Mo-BHA complex combines with the achiral oxidant to oxidize the alkene in a concerted fashion by transfer of oxygen from the metal peroxide to the alkene.78 The chiral BHA-molybdenum complex has been used for the catalytic asymmetric oxidation of sulfides and disulfides, utilizing 1 equiv. of alkyl peroxide, with yields up to 83% and ees up to 86%. An extension of the methodology combines the asymmetric oxidation with kinetic resolution providing excellent enantioselectivity (ee = 92-99%).79... 

Amidocarbonylation aldehydes, 11, 512 enamides, 11, 514 overview, 11, 511-555 Amido complexes with bis-Cp titanium, 4, 579 Group 4, surface chemistry on oxides, 12, 515 Group 5, surface chemistry on oxides, 12, 524 with molybdenum mono-Cp, 5, 556 with mono-Cp titanium(IV) alkane elimination, 4, 446 amine elimination, 4, 442 characteristics, 4, 413 via dehalosilylation reactions, 4, 448 HCL elimination, 4, 446 metathesis reactions, 4, 438 miscellaneous reactions, 4, 448 properties, 4, 437... 

Imido-nitrido complexes, with mono-Cp Ti(IV), 4, 425-426 Imido-supporting ligands, in molybdenum complexes alkenes, 5, 535 alkynes, 5, 548... 

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... 

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