Weight | 343.962 g/mol |
---|---|
Formula | C8H2Co2O8 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
Dicobalt carbonyl (10210-68-1)
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- Infrared spectroscopic studies on metal carbonyl compounds-III1: Assignment of the totally symmetric C-O stretching bands of the metal carbonyls, with special respect to the spectra of tetracobalt-dodekacarbonyl and dicobalt-octacarbonyl (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1963)
- Infrared spectroscopic studies on metal carbonyl compoundsVI: Infrared spectroscopic studies on two isomeric forms of dicobalt octacarbonyl in solutinos (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1963)
- Bis(diphenylphosphino)acetylene as Bifunctional Ligand in Dicobalt Carbonyl Complexes (Organometallics, 2002)
- Direct evidence for bridge-terminal carbonyl exchange in solid dicobalt octacarbonyl by variable-temperature magic angle spinning carbon-13 NMR spectroscopy (Journal of the American Chemical Society, 1984)
- Reactions of P2Ph4 with alkyne-bridged dicobalt carbonyl complexes; crystal structures of [Co2{-C2(CO2Me)2}(-P2Ph4)(CO)4], [Co2{-PPh2CHCPhC(O)}(-PPh2)(CO)4] and [Co2{-PPh2C(O)CHCH}(-PPh2)(CO)3(PPh3)] (Journal of The Chemical Society-dalton Transactions, 1991)
- Fundamental metal carbonyl equilibria: a quantitative infrared spectroscopic study of the equilibrium between dicobalt octacarbonyl and tetracobalt dodecacarbonyl under carbon monoxide pressure in hexane solution. (Journal of Organometallic Chemistry, 1980)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILES[CH-]=O.[CH-]=O.[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[C-]#[O+].[Co].[Co+2]
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InChIKeyBXCQGSQPWPGFIV-UHFFFAOYSA-N
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