antimony
trifluoroamine oxide
antimony pentafluoride
Conditions | Yield |
---|---|
In neat (no solvent) cylinder fiited with dry powdered element, NF3O condensed into cylinder at -196°C, mixt. heated at 210°C for 24h; not isolated, monitored by NMR, IR; | 90% |
((pentafluorosulfanyl)imino)difluorosulfane
antimonypentachloride
A
SF5N=SCl2
B
((pentafluorosulfanyl)imino)chlorofluorosulfane
C
antimony pentafluoride
Conditions | Yield |
---|---|
sulfane was condesed on SbCl5 at -196°C, heated at 100°C to initiate the reaction; fractionation through a series of traps at -6, -45, -78, -112 and -196°C in vac., a -45°C trap contained the product; | A 35% B n/a C n/a |
H2F(1+)*SbClF5(1-)=H2FSbClF5
antimony pentafluoride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: HCl, HF; decomposition above -50°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) powdered metal treated with XeF2 (air-tight autoclave, 200-300°C); |
Conditions | Yield |
---|---|
burning antimony filings in F2 atmosphere; without isolation of intermediates the end product liq. SbF5; | |
in a stream of HF-free F2; distn. in vac.; | |
In not given |
Conditions | Yield |
---|---|
HF free of water;; | |
HF free of water;; | |
at 100℃; for 3h; Autoclave; Inert atmosphere; |
Conditions | Yield |
---|---|
In hydrogen fluoride | |
In hydrogen fluoride HF (liquid); |
antimony pentafluoride
Conditions | Yield |
---|---|
With hydrogen fluoride by addn. antimonic acid into HF soln.; evapn. in vac.; cannot be crystallized; | |
With calcium fluoride; sulfuric acid by distn.; | 0% |
With hydrogen fluoride anhydrous antimonic acid with concd. HF soln.; | 0% |
Conditions | Yield |
---|---|
by glowing antimonic acid with dry HgF2; | 0% |
by glowing antimonic acid with dry HgF2; | 0% |
antimony pentafluoride
Conditions | Yield |
---|---|
With diethyl ether In dichloromethane Kinetics; byproducts: Et2O, CH3CH2F; vac. line; 298 - 343 K; | |
With 1,3-dioxolan In dichloromethane Kinetics; byproducts: Et2O, CH3CH2F; vac. line; 298 - 343 K; |
Conditions | Yield |
---|---|
With hydrogen fluoride | |
With hydrogen fluoride byproducts: HCl; with anhydrous HF excess; temp. programming is given; SbF5 in liq. form; | |
With HF byproducts: HCl; with anhydrous HF, at room temp., in dry conditions; HF excess; SbF5 in liq. form; | |
With HF byproducts: HCl; with anhydrous HF excess; temp. programming is given; SbF5 in liq. form; | |
With HF |
antimony pentafluoride
Conditions | Yield |
---|---|
byproducts: HF; at 80 °C; |
antimony pentafluoride
Conditions | Yield |
---|---|
at >240 °C; | |
at >240 °C; |
Dichlorodifluoromethane
A
antimony tetrachloride fluoride
B
antimony dichloride trifluoride
C
SbF4Cl
D
SbCl3F2
E
antimony pentafluoride
Conditions | Yield |
---|---|
In neat (no solvent) reaction at 600°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating of antimony powder and OF2; inflammation;; | |
In neat (no solvent) heating of antimony powder and OF2; inflammation;; |
perfluoro(2,4-dimethyl-3-oxa-2,4-diazapentane)
tris(trifluoromethyl)stibane
A
Perfluoro-2-azapropen
B
tris(trifluoromethyl)hydroxylamine
C
antimony pentafluoride
Conditions | Yield |
---|---|
warming from -60°C to room temp. within 10 h; | A >99 B >99 C >99 |
warming from -60°C to room temp. within 10 h; | A >99 B >99 C >99 |
Conditions | Yield |
---|---|
In neat (no solvent) dry air atmosphere; melting and thermal decompn. above 600-650°C; TGA; |
Conditions | Yield |
---|---|
In neat (no solvent) dry air atmosphere; melting and thermal decompn. above 600-650°C; TGA; |
Conditions | Yield |
---|---|
In neat (no solvent) dry air atmosphere; melting and thermal decompn. above 600-650°C; TGA; |
Conditions | Yield |
---|---|
In neat (no solvent) dry air atmosphere; melting and thermal decompn. above 600-650°C; TGA; |
antimony(V) chloride
hydrogen fluoride
A
hydrogenchloride
B
antimony pentafluoride
Conditions | Yield |
---|---|
In hydrogen fluoride solving of SbCl5 in liq. HF;; | |
In hydrogen fluoride solving of SbCl5 in liq. HF;; |
plutonium hexafluoride
antimony(III) fluoride
A
PuF4
B
antimony pentafluoride
Conditions | Yield |
---|---|
below room temp.; powder XRD; |
iridium hexafluoride
antimony(III) fluoride
A
iridium pentafluoride
B
antimony pentafluoride
Conditions | Yield |
---|---|
In neat (no solvent) IrF6 condensed onto excess of SbF3 at -196°C, allowed to warm slowly to room temp.; volatiles species removed, fractionated; IR; |
chromium pentafluoride
KrF(1+)*SbF6(1-) = [KrF][SbF6]
A
hexafluoro-chromium(VI)
C
antimony pentafluoride
D
fluorine
Conditions | Yield |
---|---|
34°C; | A 0% B n/a C n/a D n/a |
Conditions | Yield |
---|---|
partial decompn. in wet air; | |
partial decompn. in wet air; |
fluoro(trifluoromethylsulfenyl)phosphonium SbF6
antimony pentafluoride
Conditions | Yield |
---|---|
In liquid sulphur dioxide byproducts: HF, (CF3SP)99; |
ruthenium(VI) fluoride
antimony(III) fluoride
A
ruthenium(V) fluoride
B
antimony pentafluoride
Conditions | Yield |
---|---|
RuF6 was condensed onto SbF3 at -196°C; was allowed to warm slowly to room temperature; volatiles were removed; IR; |
antimonypentachloride
B
antimony(III) chloride
C
antimony pentafluoride
Conditions | Yield |
---|---|
With HF byproducts: HCl, Cl2; with anhydrous HF; distn. (8h) at 90 °C (distn. of HCl and HF), and up to 125 °C (distn. of SbCl5, SbCl3 and SbF5); distn. at 390 °C; |
A
antimony pentafluoride
B
phosphorus pentafluoride
Conditions | Yield |
---|---|
in soln.; 194 K; 30 min; | A >99 B >99 |
NF2O(1+)*SbF6(1-) = (NF2O)(SbF6)
A
trifluoroamine oxide
B
antimony pentafluoride
antimony pentafluoride
Conditions | Yield |
---|---|
In liquid sulphur dioxide under Ar; recrystn. (SO2), elem. anal.; | 100% |
Ph3GeCo(CO)4
antimony pentafluoride
triphenylgermanium fluoride
Conditions | Yield |
---|---|
With pyrographite In diethyl ether under N2 a soln. of Co-complex in ether was added dropwise with stirring to a suspension of SbF5/C in ether at room temp., stood for 6 d; monitored by IR, filtered, pumped off, dissolved in pentane, filtered, cocnd., cooled to -20°C; | 100% |
indium(I) tetrafluoroborate
hydrogen fluoride
antimony pentafluoride
indium(I) hexafluoroantimonate
Conditions | Yield |
---|---|
In hydrogen fluoride HF (liquid); equimol., HF condenced onto reagent at 77 K, alowed to warm to room temp., left for 1 d; volatiles removed (vac.); elem. anal.; | 100% |
(2,3,7,8,12,13,17,18-octaethylporphyrinato)zinc(II)
antimony pentafluoride
Conditions | Yield |
---|---|
In dichloromethane at -78 - 20℃; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: hydrogen fluoride; antimony pentafluoride at -196 - 20℃; Sealed tube; Stage #2: acetonitrile at -196 - 20℃; for 0.5h; Sealed tube; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
Stage #1: hydrogen fluoride; antimony pentafluoride at -196 - 20℃; Sealed tube; Stage #2: acetonitrile at -196 - 20℃; for 0.5h; Sealed tube; Inert atmosphere; | 100% |
Conditions | Yield |
---|---|
at -196 - -64℃; for 0.166667h; Sealed tube; | 100% |
Conditions | Yield |
---|---|
at -196 - -64℃; for 0.166667h; Sealed tube; | 100% |
Conditions | Yield |
---|---|
at -196 - -64℃; for 0.166667h; Sealed tube; | 100% |
Conditions | Yield |
---|---|
In sulfur dioxide condensation of SbF5 in SO2 into a soln. of Ti-compd. in SO2 at -50°C, warming to room temp. with stirring, then stirring at room temp. for 30 min; cooling to 10-15°C and condensation of SO2, formation of a solid, elem. anal.; | 99.8% |
cis-difluorodiazene
antimony pentafluoride
N2F(1+)*SbF6(1-)=[N2F][SbF6]
Conditions | Yield |
---|---|
In hydrogen fluoride HF (liquid); (vac.); condensing HF onto SbF5 at -196°C, warming to room temp.,addn. of N2F2 at -196°C, warming to room temp., stirring for 10 min; pumping off at -64°C for 2 h; | 99.7% |
cis-osmium tetrafluoride dioxide
antimony pentafluoride
B
[OsO2F3](1+)*[SbF6](1-)=[OsO2F3][SbF6]
Conditions | Yield |
---|---|
In hydrogen fluoride HF (liquid); SbF5 added to OsO2F4, HF condensed at -196°C, warmed to room temp.; pptd. at -78°C, pumped for 5 h at 0°C; | A 99.4% B 0% |
In neat (no solvent) warmed to room temp.; pumped at 0°C for 6 d; | A 107 % B 0% |
bis(pentafluoroethyl)selenium difluoride
antimony pentafluoride
Conditions | Yield |
---|---|
20°C, 1.5 h; | 99% |
carbon monoxide
antimony pentafluoride
Conditions | Yield |
---|---|
mild conditions, low CO pressure; | 99% |
krypton difluoride
antimony pentafluoride
KrF(1+)*SbF6(1-) = [KrF][SbF6]
Conditions | Yield |
---|---|
In hydrogen fluoride dry HF was distd. in 1 equiv of SbF5, homogenized at ambient temp., 1.06 equiv of KrF2 was transferred under vac. at -196°C, warmed to room temp., cooled, warmup was repeated three cycles; volatiles pumped off at -22°C; | 99% |
Conditions | Yield |
---|---|
In further solvent(s) byproducts: COF2; absence of air and moisture; stirring AuCl3 in SbF5 under 0.6 atm CO (60-70°C, 5 d); evapn. (vac., 55°C); | 99% |
carbon monoxide
antimony pentafluoride
Conditions | Yield |
---|---|
mild conditions, low CO pressure; | 99% |
carbon monoxide
antimony pentafluoride
Conditions | Yield |
---|---|
mild conditions, low CO pressure; | 99% |
fluoroformyl chloride
antimony pentafluoride
(COClF)SbF5
Conditions | Yield |
---|---|
In neat (no solvent) Teflon ampoule inside stainless-steel vac. line; excess COClF, mixing at-196°C, stirring at -78°C for 1 h; pumping at -110°C; | 99% |
Conditions | Yield |
---|---|
In neat (no solvent) Teflon ampoule inside stainless-steel vac. line; excess COF2, mixing at -196°C, stirring at -78°C for 1 h; pumping at -126°C; | 99% |
carbon monoxide
antimony pentafluoride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: CO2, S2O5F2, Sb2F9(SO3F); liquid SbF5, ca. 1 atm CO, 60-90°C, 2-4 d; | 99% |
With HF byproducts: CO2, S2O5F2, Sb2F9(SO3F); to the reactor charged with Os(SO3F)3 were added SbF5 and HF using a stainless steel vac. line, at -195°C CO was admitted to the reactor,heated to 50-60°C for 1-2 days without stirring; volatiles were removed in vac., crystals were washed with an SbF5/HF (2:1) mixt., volatiles were removed in vac.; | 87% |
heating at 60-90°C in 1 atm CO; |
Reported in EPA TSCA Inventory. Antimony and its compounds are on the Community Right-To-Know List. EPA Extremely Hazardous Substances List.
OSHA PEL: TWA 0.5 mg(Sb)/m3
ACGIH TLV: TWA 0.5 mg(Sb)/m3
NIOSH REL: (Antimony) TWA 0.5 mg(Sb)/m3
DOT Classification: 8; Label: Corrosive, Poison
The Antimony(V) pentafluoride with the cas number7783-70-2, is also called (1) Antimony (V) fluoride ; (2) Antimony fluoride ; (3) Antimony fluoride (SbF5) ; (4) Antimony pentafluoride ; (5) Antimony(V) fluoride ; (6) Antimony(V) pentafluoride ; (7) Pentafluoroantimony . It belongs to the following Product Categories: (1)Inorganics; (2)Inorganic Fluorides; (3)Antimony Salts; (4)Metal and Ceramic Science; (5)Salts
The Antimony(V) pentafluoride is a colorless, oily liquid. It is quite toxic by inhalation, in contact with skin and if swallowed. Hence,when you are using this chmical, please wear suitable protective clothing, gloves and eye/face protection. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. After contact with skin, wash immediately with plenty of soap-suds and take off immediately all contaminated clothing. If you feel unwell, seek medical advice immediately (show the label whenever possible.) Besides, It is toxic to aquatic organisms, may cause long-term adverse effects in the aquatic environment, so avoid release to the environment refering to special instructions / safety data sheets.
You can still convert the following datas into molecular structure :
1. [F-].[F-].[F-].[F-].[F-].[SbH3+3]
2. InChI=1/5FH.Sb.3H/h5*1H;;;;/q;;;;;+3;;;/p-5/r5FH.H3Sb/h5*1H;1H3/q;;;;;+3/p-5
The Antimony(V) pentafluoride toxic data can be showed in the following sheet.|
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mouse | LC50 | inhalation | 270mg/m3 (270mg/m3) | LUNGS, THORAX, OR RESPIRATION: OTHER CHANGES LIVER: OTHER CHANGES KIDNEY, URETER, AND BLADDER: OTHER CHANGES | Gigiena i Sanitariya. For English translation, see HYSAAV. Vol. 35(7), Pg. 25, 1970. |
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