Hexa(tert-butoxy)ditungsten(III) is a coordination complex of tungsten(III). It is one of the homoleptic alkoxides of tungsten. A red, air-sensitive solid, the complex has attracted academic attention as the precursor to many organotungsten derivatives. It an example of a charge-neutral complex featuring a W≡W bond, arising from the coupling of a pair of d3 metal centers.
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3D model (JSmol) | |
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Properties | |
C24H54O6W2 | |
Molar mass | 806.37 g·mol−1 |
Appearance | red solid |
Density | 1.651 g/cm3 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). |
Hexa(tert-butoxy)ditungsten(III) was first discovered by M. H. Chisholm and M. Extine in 1975. [1] They synthesized hexa(tert-butoxy)ditungsten(III) by reacting tungsten(III) dialkylamides with t-BuOH in organic solvents. They also found that W2(O-t-Bu)6 reacts with carbon dioxide in toluene to form green W2(O-t-Bu)4(O2CO-t-Bu)2 under room temperature. In CO2, these compounds can be separated from cooled toluene purely. Without the presence of CO2, W2(O-t-Bu)4(O2CO-t-Bu)2 is regenerated into W2(O-t-Bu)6 reversibly.
W2(O-t-Bu)6 can also be synthesized by using NaW2Cl7(THF)5 as reactant in THF with addition of NaO-t-Bu under ambient temperature for 18 hours. [2] [3] After the reaction, the solvent is removed, and it becomes a red slurry. Further cooling (-35oC) and decantation or vacuum filtration separate red crystalline W2(O-t-Bu)6. The salt metathesis reaction from the THF complex of ditungsten heptachloride is as follows:
NaW2Cl7(THF)5 + 6 NaO-t-Bu → W2(O-t-Bu)6 + 7 NaCl + 5 THF
These needle-like red crystals are highly unstable under oxygen and water and can be dissolved in most organic solvents such as diethyl ether and pentane. They are found in dimers with two tungsten(III) bond with each other to form triple bonds. These two W(III) form pseudotetrahedral center and adopt a staggered, ethane-like conformation, similar to its dimolybdenum analogue. The structure of the compound was investigated by Chisholm and his team using single crystal X-ray diffraction. The investigation was performed in a C-centered monoclinic crystal. In C2/c space group, there is one half inversion center molecule and one whole molecule in general position. There are several orientations for each position which leads to the length of WW ranging from 1.74 to 2.53 Å. The orientation of t-butyl groups in each W are one direct away from WW (distal) and two over WW (proximal). This arrangement had been calculated as the best to minimize the steric repulsing effect.
This compound can be decomposed into WO2, t-BuOH, and isobutylene, with trace amount of water under 200oC. This compound can react easily with alkynes or nitriles to generate RC≡W(O-t-Bu)3 or both RC≡W(O-t-Bu)3 and N≡W(O-t-Bu)3. With excess amount of nitrile, only N≡W(O-t-Bu)3 are formed along with RC≡CR. RC≡W(O-t-Bu)3 is important catalyst for alkyne metathesis while N≡W(O-t-Bu)3 is a catalyst for nitrogen exchange of nitriles. The C≡W bond in RC≡W(O-t-Bu)3 was concluded to behave as polarized C(-)≡W(+). Thus, the metathesis catalytic reaction starts with tungsten as electrophilic attacker to attack acetylene and followed by alkylidyne carbon as nucleophilic attacker to attack acetylenic carbon atom.
Carbon monoxide can react with W2(O-t-Bu)6 to form W2(O-t-Bu)6(CO). This compound has a carbonyl group that acts as a bridge between two W(III) atoms and has a similar structure to cyclopropenone. This compound can further react with i-PrOH to generate W4(μ-CO)2(O-i-Pr)12.
Schrock first reported the “Chop Chop Reaction”, which is the cleavage of C≡C and W≡W bonds into the formation of C≡W bonds: [5]
W2(O-t-Bu)6 + RC≡CR → 2[RC≡W(O-t-Bu)3]
Where R can be Me, Et, Pr. The reaction happens at around 25 oC in less than an hour. The reaction rate increases in the following order: 4-octyne, 3-hexyne, 2-butyne. The resulting compounds are all colorless and sublime at room temperature. However, W2(O-t-Bu)6 doesn’t react with PhC≡CPh or Me3SiC≡CSiMe3. It is because of unfavorable electronics and steric effects respectively. Instead, it can react with two equivalents of EtC≡CPh, EtC≡CSiMe3, or EtC≡C–CH=CH2 to form corresponding RC≡W(O-t-Bu)3 compounds (R = Ph, SiMe3, HC=CH2). W2(O-t-Bu)6 reacts more easily with asymmetric substitute acetylenes than symmetric ones:
W2(O-t-Bu)6 + 2EtC≡CR → 2[RC≡W(O-t-Bu)3] + EtC≡CEt
This reaction includes an alkyne adduct on the μ-perpendicular site to increase both the length of WW bonds and CC (alkyne) bonds. This intermediate can be analogue as a dimetallatetrahedranes and further react into RC≡W(O-t-Bu)3 with internal redox reaction. The resulting RC≡W(O-t-Bu)3 is a catalyst for metathesis reactions. RC≡W(O-t-Bu)3 can react with normal alkynes for metathesis reactions and also with terminal alkynes for both metathesis reactions and polymerizations. [6]
Besides simple metathesis reactions, W2(O-t-Bu)6 also reacts with 3-hexyne in a 1:1 molar ratio to form a triangular tritungsten complex compound [W3(O-t-Bu)5(μ-O)(μ-CEt)O]2. [7] This reaction takes about 3 days under 75-80 oC in toluene. This reaction has a two steps mechanism; first is the C≡C and W≡W metathesis reaction and follow by formal addition of carbyne (W≡C) to alkoxide (W2):
W2(O-t-Bu)6 + RC≡CR → 2[RC≡W(O-t-Bu)3]
W2(O-t-Bu)6 + RC≡W(O-t-Bu)3 → W3(O-t-Bu)5(μ-O)(μ-CEt)O → [W3(O-t-Bu)5(μ-O)(μ-CEt)O]2
W2(O-t-Bu)6 also reacts with EtC≡CC≡CEt to form (t-Bu-O)3W≡CC≡W(O-t-Bu)3:
W2(O-t-Bu)6 + EtC≡CC≡CEt → (t-Bu-O)3W≡CC≡W(O-t-Bu)3 + EtC≡CEt
This compound, however, does not act as a metathesis catalyst.
Similar to the reaction with alkynes, W2(O-t-Bu)6 react with RC≡N by “Chop Chop reaction” in a ratio of 1:1 to form equivalent amount of RC≡W(O-t-Bu)3 and N≡W(O-t-Bu)3: [8]
W2(O-t-Bu)6 + RC≡N → RC≡W(O-t-Bu)3 + N≡W(O-t-Bu)3
Although W2(O-t-Bu)6 reacts with nitriles, it doesn’t react with nitrogen (N≡N).
When C≡C and C≡N bond both exist, W2(O-t-Bu)6 reacts more rapidly with C≡N than C≡C bond. Here’s an example of W2(O-t-Bu)6 reacting with EtC≡CCN in the presence of quinuclidine:
W2(O-t-Bu)6 + EtC≡CCN + 12quin → EtC≡CC≡W(O-t-Bu)3(quin) + N≡W(O-t-Bu)3
On the other hand, the metathesis catalyst MeC≡W(O-t-Bu)3 reacts more rapidly with C≡C than C≡N bond. Similar reaction with EtC≡CCN and quinuclidine produce different product:
MeC≡W(O-t-Bu)3 + EtC≡CCN + 12quin → NCC≡W(O-t-Bu)3(quin) + EtC≡CMe
Cotton successfully reacted W2(O-t-Bu)6 with nitrosobenzene to synthesize a three-bridge compound [W(O-t-Bu)2(NPh)]2(μ-O)(μ-O-t-Bu)2. This reaction undergoes two oxidative additions to form W=N bonds. However, they couldn’t figure out where the one missing oxygen went. This reaction is the first discovered reaction of a nitroso with metal multiple bonds.
W2(O-t-Bu)6 can also react with allene (H2C=C=CH2) for adduction. In a ratio of 1:1, allene adduct on W2 to form a v-shape bridge structure:
W2(O-t-Bu)6 + H2C=C=CH2 → W2(O-t-Bu)6(C3H4)
This compound is synthesized under 0oC in hexane and crystallized under -72oC. It decomposes easily in solution at 0oC and in crystalline state at ~25oC but very stable at ~20oC. The bridging allene is parallel to the W2 bond. In a ratio of 1:2, the additional allene will bind to single metal center as typical bonding:
W2(O-t-Bu)6(C3H4) + 2H2C=C=CH2 → W2(O-t-Bu)6(C3H4)2
The product of 1:1 adduction can further react with carbon monoxide to form a similar structure to 1:2 adduction but adducted with carbon monoxide instead of allene:
W2(O-t-Bu)6(C3H4) + 2CO → W2(O-t-Bu)6(C3H4)(CO)2
Reaction using methylallene (MeHC=C=CH2) instead of allene is also feasible forming similar structures.
W2(O-t-Bu)6 can react with trans-Pt(C≡CH)2(PMe2Ph)2 to form (t-Bu-O)3W≡C–C≡W(O-t-Bu)3 and trans-(PMe2Ph)2Pt[C2W2(O-t-Bu)5]2.
In organic chemistry, an alkene, or olefin, is a hydrocarbon containing a carbon–carbon double bond. The double bond may be internal or in the terminal position. Terminal alkenes are also known as α-olefins.
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A triple bond in chemistry is a chemical bond between two atoms involving six bonding electrons instead of the usual two in a covalent single bond. Triple bonds are stronger than the equivalent single bonds or double bonds, with a bond order of three. The most common triple bond is in a nitrogen N2 molecule; the second most common is that between two carbon atoms, which can be found in alkynes. Other functional groups containing a triple bond are cyanides and isocyanides. Some diatomic molecules, such as diphosphorus and carbon monoxide, are also triple bonded. In skeletal formulae the triple bond is drawn as three parallel lines (≡) between the two connected atoms.
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Molybdenum(III) chloride is the inorganic compound with the formula MoCl3. It forms purple crystals.
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Hexa(tert-butoxy)dimolybdenum(III) is a coordination complex of molybdenum(III). It is one of the homoleptic alkoxides of molybdenum. An orange, air-sensitive solid, the complex has attracted academic attention as the precursor to many organomolybdenum derivatives. It an example of a charge-neutral complex featuring a molybdenum to molybdenum triple bond (Mo≡Mo), arising from the coupling of a pair of d3 metal centers. It can be prepared by a salt metathesis reaction from the THF complex of molybdenum trichloride and lithium tert-butoxide:
Lithium tert-butoxide is the metalorganic compound with the formula LiOC(CH3)3. A white solid, it is used as a strong base in organic synthesis. The compound is often depicted as a salt, and it often behaves as such, but it is not ionized in solution. Both octameric and hexameric forms have been characterized by X-ray crystallography
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