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CAS No.: | 1282-37-7 | ||||||||||
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Name: | FERROCENIUM TETRAFLUOROBORATE | ||||||||||
Article Data: | 15 | ||||||||||
Molecular Structure: | |||||||||||
Formula: | C10H10BF4Fe10* | ||||||||||
Molecular Weight: | 272.841 | ||||||||||
Synonyms: | FERROCENIUM TETRAFLUOROBORATE;FERROCENIUM TETRAFLUOROBORATE, TECH. | ||||||||||
Melting Point: |
178 °C (dec.)(lit.) |
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Boiling Point: |
Vapour density: |
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Solubility: | Toxicity data (The meaning of any toxi">
Stability
Toxicology
Toxicity data |
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Appearance: | solid | ||||||||||
Hazard Symbols: | |||||||||||
Risk Codes: | 34 | ||||||||||
Safety: |
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PSA: | 0.00000 | ||||||||||
LogP: | 2.35650 |
tetrafluoroboric acid diethyl ether
ferrocene
ferrocenium(III) tetrafluoroborate
Conditions | Yield |
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In nitromethane; dichloromethane addn. of nitromethane to Fe complex soln. (CH2Cl2) under Ar; addn. of HBF4*Et2O in two portions; stirring, 1h; evapn.; extn. (pentane); stirring with ether; dissoln. in heated CH3CN; filtration through Na2SO4 (free from water) in ether; pptn.; drying (high vac.); elem. anal.; | 95% |
Conditions | Yield |
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In tetrahydrofuran byproducts: Ag; (Ar or N2), ferrocene in THF treated with 0.8 equiv. of AgBF4 in THF at -78°C; filtered, evapd.(vac.), extd.(CH2Cl2), crystd. at room temp.; | 87% |
Conditions | Yield |
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In diethyl ether; nitromethane; dichloromethane 12 h;; removing solvent; extn. with petroleum ether 4 times (40-60°C); stirring with ether; filtn.; drying; elem.anal.;; | 78% |
With p-benzoquinone In diethyl ether; water |
Conditions | Yield |
---|---|
With boron trifluoride diethyl etherate; oxygen In not given passing O2 trough soln. of ferrocene and boron trifluoride etherate;; | 45% |
With O2; boron trifluoride etherate In not given passing O2 trough soln. of ferrocene and boron trifluoride etherate;; | 45% |
With p-benzoquinone In benzene addn. of BF3 or boron trifluoride etherate soln. of ferrocene and p-benzoquinone in benzene;; | |
With BF3 or boron trifluoride etherate; p-benzoquinone In benzene addn. of BF3 or boron trifluoride etherate soln. of ferrocene and p-benzoquinone in benzene;; |
Conditions | Yield |
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With oxygen In diethyl ether byproducts: O2(2-); presence of BF3;; | |
With O2 In diethyl ether byproducts: O2(2-); presence of BF3;; |
ferrocene
tetrabutylammonium tetrafluoroborate
ferrocenium(III) tetrafluoroborate
Conditions | Yield |
---|---|
In acetonitrile Electrochem. Process; Ar atmosphere; oxidn. (Pt mesh, 48.0 C); removal of MeCN (vac., room temp.), no further purification; |
sodium tetrafluoroborate
ferrocenium(III) tetrafluoroborate
Conditions | Yield |
---|---|
In water cooling to -5°C, filtration, washing with water, then with THF, drying in vac.; |
Conditions | Yield |
---|---|
In dichloromethane prepn. by oxidn. of Cp2Fe with nitrosonium tetrafluoroborate; | |
In dichloromethane |
cyclopentadienyl iron(II) dicarbonyl dimer
ferrocenium(III) tetrafluoroborate
dimethylsulfide
Conditions | Yield |
---|---|
In dichloromethane byproducts: (C5H5)2Fe; addn. of ferricinium compd. to Fe complex soln. in the presence of SMe2under Ar; filtration; evapn. to 1/3 the volume; addn. of ether/pentane 3/1); pptn.; thoroughly washing (ether, pentane); drying (high vac.); | 99% |
ferrocenium(III) tetrafluoroborate
dicarbonyl(η5-cyclopentadienyl)(η1-7-methoxy-1-cycloheptenyl)iron
A
ferrocene
B
dicarbonyl(η5-cyclopentadienyl)(η1-7-methoxycycloheptene-1-carbonyl)iron
Conditions | Yield |
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With `CO In dichloromethane Addn. of Cp2FeBF4 to iron-compd. (methylene chloride, 55 psiCO, 1h).; Removal of solvent (vacuo), elution with hexane (alumina column) gives yellow band of ferrocene, elution with CH2Cl2 gives yellow band of dicarbonyl complex, elem. anal.; | A n/a B 99% |