Organomolybdenum chemistry


Organomolybdenum chemistry is the chemistry of chemical compounds with Mo-C bonds. The heavier group 6 elements molybdenum and tungsten form organometallic compounds similar to those in organochromium chemistry but higher oxidation states tend to be more common.

Mo(0) and more reduced states

is the precursor to many substituted derivatives. It reacts with organolithium reagents to give anionic acyls which can be O-alkylated to give Fischer carbenes.
Mo6 reacts with arenes to give piano-stool complexes such as molybdenum tricarbonyl. Cycloheptatrienemolybdenum tricarbonyl, which is related to Mo3, reacts with trityl salts to give the cycloheptatrienyl complex:
.
Reduction of Mo6 gives 2− which is formally Mo.
CO-free Mo compounds tend to be more reducing and kinetically labile than the carbonyl complexes. Examples include bismolybdenum and trismolybdenum. Such compounds can be prepared by metal vapor synthesis and reductive routes from molybdenum chloride.

Mo(II)

Halogenation of Mo6 gives Mo carbonyl halides, which are also versatile precursors. One large collection of compounds have the formula Mo3X, derived from cyclopentadienylmolybdenum tricarbonyl dimer.
Treating molybdenum acetate with methyllithium gives Li4.

Mo(IV)

With the formula of the type Cp2MoX2 molybdocene dichloride and molybdocene dihydride are both known as are ansa metallocene analogues.
.

Mo(V) and Mo(VI)

Mo5, Mo6, and salts of - are known.
Oxo and imide ligands are found in several high oxidation state organomolybdenum compounds. The complexes MoO2X are illustrative. Schrock's Mo-based olefin metathesis catalysts feature molybdenum centers supported by alkoxide, alkylidene, and imido ligands.

Organotungsten compounds

Tungsten analogues of almost all organoMo compounds are known. Some notable examples include hexamethyltungsten and analogues of Schrock olefin metathesis catalysts.

Applications

Mo-based catalysts are useful for olefin metathesis.
Trisamidomolybdenum alkylidyne complexes catalyze alkyne metathesis.
In the Kauffmann olefination, molybdenum chloride and methyllithium form an organometallic complex capable of carbonyl olefination.