CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER
CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Basic information
- Product Name:
- CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER
- Synonyms:
-
- Bis-(cyclopentadienyl)-molybdenum tricarbonyl
- (Cyclopentadienyl)tricarbonylmolybdenum dimer
- Bis[(eta5-cyclopentadienyl)tricarbonylmolybdenum]
- Bis[(pi-cyclopentadienyl)molybdenum tricarbonyl]
- Bis[tricarbonyl(eta5-cyclopentadienyl)molybdenum]
- Di(mu-carbonyltetracarbonyl)di(pi-cyclopentadienyl)dimolybdenum
- Di[(pi-cyclopentadienyl)tricarbonylmolybdenum]
- Hexacarbonylbis(eta5-cyclopentadienyl)dimolybdenum(i)
- CAS:
- 12091-64-4
- MF:
- C16H10Mo2O610*
- MW:
- 490.13
- EINECS:
- 235-156-0
- Product Categories:
-
- Catalysis and Inorganic Chemistry
- Chemical Synthesis
- metallocene
- Molybdenum
- MolybdenumVapor Deposition Precursors
- Precursors by Metal
- Mol File:
- 12091-64-4.mol
CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Chemical Properties
- Melting point:
- 222 °C (dec.)(lit.)
- form
- crystal
- color
- red to purple
- Water Solubility
- It is insoluble in water.
- Sensitive
- Air Sensitive
- Exposure limits
- ACGIH: TWA 10 mg/m3; TWA 3 mg/m3
NIOSH: IDLH 5000 mg/m3 - InChI
- 1S/2C5H5.6CO.2Mo/c2*1-2-4-5-3-1;6*1-2;;/h2*1-5H;;;;;;;;
- InChIKey
- XCUPBPUEWLTPMQ-UHFFFAOYSA-N
- SMILES
- [Mo][Mo].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[CH]1[CH][CH][CH][CH]1.[CH]2[CH][CH][CH][CH]2
MSDS
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
CYCLOPENTADIENYLMOLYBDENUM TRICARBONYL DIMER Usage And Synthesis
Chemical Properties
red to purple glistening crystals or powder
Uses
It is widely used as a chemical intermediate in the laboratories, manufacture purposes, chemical and pharmaceutical intemediate.
reaction suitability
core: molybdenum
reagent type: catalyst
Synthesis
Tricarbonyl(Η-cyclopentadienyl)manganese dimerization was prepared as follows: tetrahydrofuran (THF, 45 ml) was added to 18.8 mmol of cyclopentadiene, and after cooling to -78 ??C, 12.5 ml (18.8 mmol) of Bu-Li was added drop-wise, and pentamethylcyclopentadienyl lithium was coordinated. Then 5 g (18.8 mmol) of molybdenum hexacarbonyl was added to the substance and heated at reflux for 48 hours, and when the reaction was complete, the mother liquor was cooled to 0 ??C. Separately, 3.2 g (18.8 mmol) of ferrous sulfate (II) was added to a solution comprising a mixture of 100 ml of pure water and 20 ml of acetic acid, and the solution so obtained was added dropwise to the mother liquor. The resulting red solution was made to undergo suction filtration, washing and drying, and the manganese tricarbonyl (Η-cyclopentadienyl)-co-manganese dimer complex was obtained by recrystallization. The yield was 20%.
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