benzyl fluoride
ytterbium(III) fluoride
Conditions | Yield |
---|---|
In toluene under N2, ambient temp., 1 h; filtered, washed with toluene, dried in vacuo; elem. anal.; |
Conditions | Yield |
---|---|
In hydrogenchloride dissolving oxide in aq. HCl, pptn. with excess aq. NH4F, filtration, drying, dehydration on heating ppt. with excess powdered NH4F to 360°C in a dry stream of He or Ne (O2-free) for 5h;; | |
In neat (no solvent) excess fluoride, 200°C, Pt-vessel; removal of excess fluoride on heating in a stream of dry inert gas to 450°C;; | |
In hydrogenchloride dissolving oxide in aq. HCl, pptn. with excess aq. NH4F, filtration, drying, dehydration on heating ppt. with excess powdered NH4F to 360°C in a dry stream of He or Ne (O2-free) for 5h;; | |
With HF In hydrogen fluoride aq. HF; lanthanide trifluoride is treated with 40% hydrofluoric acid with stirring, decanting the HF, drying under an infrared heater at 50°C, mixing with NH4F, heating at 500°C; XRD, DTA; | |
With HNO3 In nitric acid prepn. by dissolving metal oxide in nitric acid followed by pptn. by ammonium fluoride and annealing of ppt. at 600°C; |
Conditions | Yield |
---|---|
In melt from nitrate and NaF dissolved in molten NaNO3;; | |
In melt from nitrate and NaF dissolved in molten NaNO3;; |
Conditions | Yield |
---|---|
With sodium linoleate; linoleic acid In ethanol; water High Pressure; Na linoleate, linoleic acid and EtOH mixed under agitation; aq. soln. ofYb(NO3)3 and NaF added; agitated for ca. 5 min; transefrred to autoclav e; sealed; hydrothermally treated at 100-200°C for 8-10 h; cooledto room temp.; deposit dispersed in cyclohexane; EtOH added; centrifuged; powder purified with EtOH several times; detd. by X-ray powder diffraction and electron microscopy; YbF3 and NaYb2F7 nanocrystals obtained; |
Conditions | Yield |
---|---|
In neat (no solvent) determination of react.-enthalpy at 298K;; |
sulfuric acid
A
ytterbium(III) fluoride
Conditions | Yield |
---|---|
In sulfuric acid aq. H2SO4; decompn. after treatment with 30% H2SO4 after several h; |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: oxygen; explosive convertion at 330-380°C, starting of fluorination at 330°C; |
Conditions | Yield |
---|---|
In neat (no solvent) at room temp. in presence of moisture;; | 0% |
Conditions | Yield |
---|---|
With sodium linoleate; linoleic acid In ethanol; water High Pressure; Na linoleate, linoleic acid and EtOH mixed under agitation; aq. soln. ofYb(NO3)3 and NH4HF2 added; agitated for ca. 5 min; transefrred to autoc lave; sealed; hydrothermally treated at 100-200°C for 8-10 h; cooled to room temp.; deposit dispersed in cyclohexane; EtOH added; centrifuged; powder purified with EtOH several times; detd. by X-ray powder diffraction and electron microscopy; YbF3 nanocrystals obtained; |
ytterbium(III) fluoride
Conditions | Yield |
---|---|
With HF byproducts: H2O; dehydration in HF flow at increasing temp. up to calcination at 800°C; | |
byproducts: H2O; vac. dehydration; sublimation twice (tantalum tube under dynamic high vac.); | |
In neat (no solvent) annealing under N2/HF stream (800°C, Pt crucible, vitreous carbontube furnace); X-ray powder diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent) fluorine passing into reaction vessel with rare earth metal (const. temp. 510°); gravimetric monitoring; |
A
ytterbium(III) fluoride
B
Carbonyl fluoride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: SO2; heated under nitrogen (rate: 10°C/min); |
Conditions | Yield |
---|---|
In hydrogenchloride byproducts: CO2; pH 1 to <4, heating to 60-100°C for 4h while stirring, washing with H2O until neutral react.;; | >95 |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: H2O; at elevated temp.;; | |
In neat (no solvent) byproducts: H2O; formation of hydrated compound with moist HF at 150-250°C, dehydration at 350-550.degreee.C with dry HF containing 10% H2;; | |
In neat (no solvent) byproducts: H2O; on passing dry HF-gas over oxide at 700°C, 200% excess HF, cooling to room temp. under diminished pressure, removal of HF by passing through He;; | 99.90-99.98 |
Conditions | Yield |
---|---|
In hydrogenchloride byproducts: CO2, CaCl2; pH 1 to <4, heating to 60-100°C for 4h while stirring, washing with H2O until neutral react.;; | >95 |
Conditions | Yield |
---|---|
In melt byproducts: CdO; with molten CdO;; | 0% |
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: carbon; violent react.;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating oxide and excess SF4 in vac. until start of react., exclusion of moisture;; | |
In neat (no solvent) heating oxide and excess SF4 in vac. until start of react., exclusion of moisture;; |
Conditions | Yield |
---|---|
In neat (no solvent) at 750°C, exothermic react.;; |
Conditions | Yield |
---|---|
In neat (no solvent) excess fluoride, 200°C, Pt-vessel; removal of excess fluoride on heating in a stream of dry inert gas to 450°C;; |
ytterbium(III) fluoride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: COF2, SO2; thermal decompn. in inert atmosphere (exclusion of moisture);; | |
In neat (no solvent, solid phase) byproducts: SO2, CO2, CF3OCF3; 600°C; elem. anal.; | |
In neat (no solvent) byproducts: COF2, SO2; thermal decompn. in inert atmosphere (exclusion of moisture);; |
Conditions | Yield |
---|---|
React. of starting materials (N2, 450°C, 3 d).; |
Conditions | Yield |
---|---|
In neat (no solvent) 200°C, excess NH4HF2; excess NH4HF2 removal on evac. at higher temp.; |
Conditions | Yield |
---|---|
In benzene-d6 under N2; |
Conditions | Yield |
---|---|
In neat (no solvent) complete dehydration without formation of oxide fluoride, heating with HF-gas at 600°C (normal pressure);; | A >99 B >99 |
In neat (no solvent) complete dehydration without formation of oxide fluoride, heating with HCl-gas at 250°C and about 40Torr;; | A >99 B >99 |
In neat (no solvent) complete dehydration without formation of oxide fluoride, heating with NH4F or NH4F*HF to 650-700°C;; | A >99 B >99 |
B
ytterbium(III) fluoride
Conditions | Yield |
---|---|
In neat (no solvent) equilibrium-react., determination of thermodynamic data of vaporization-react.;; investigation of react. by gravimetric, analytical, X-ray- and MS-measurements;; |
A
ytterbium(III) fluoride
C
water
Conditions | Yield |
---|---|
In neat (no solvent) decompn. on heating to 480°C;; |
A
ytterbium(III) fluoride
B
water
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Yb-fluoride hydroxide; on heating to 300°C;; |
Conditions | Yield |
---|---|
In neat (no solvent) decompn. on cooling slowly;; |
Conditions | Yield |
---|---|
In melt metal:metal fluoride:S molar ratio was 2:1:3, quartz crucible, Pt-capsula, several days, 850 °C; equimolar amt. of NaCl was used as flux; NaCl was washed out with water; | 99% |
strontium(II) carbonate
ytterbium(III) fluoride
silica gel
Conditions | Yield |
---|---|
With ammonium fluoride mixt. (1 mol-% Yb) firing (NH4F as flux), final firing in N2/H2 (3:1); |
Conditions | Yield |
---|---|
In neat (no solvent) mixt. annealing (sealed platinum tube, 1000-1100°C, 3 d), quenching or slow cooling to room temp.; X-ray diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent) mixt. annealing (sealed platinum tube, 1000-1100°C, 3 d), quenching or slow cooling to room temp.; X-ray diffraction, thermal anal.; |
Conditions | Yield |
---|---|
In neat (no solvent) mixt. annealing (sealed platinum tube, 1000-1100°C, 3 d), quenching or slow cooling to room temp.; X-ray diffraction; |
Conditions | Yield |
---|---|
In melt melting under CF4; |
Conditions | Yield |
---|---|
In melt melting under CF4; | |
In melt melting under CF4 according to M. Ito, G. Goutaudier, Y. Guyot, K. Lebbou, T. Fukuda, G. Boulon, J. Phys.: Condens. Matter 16 (2004) 1501-1521; |
Conditions | Yield |
---|---|
In melt melting under CF4; |
Conditions | Yield |
---|---|
In melt melting under CF4; |
Conditions | Yield |
---|---|
In melt melting under CF4; |
ytterbium(III) fluoride
Conditions | Yield |
---|---|
With lithium In neat (no solvent) byproducts: LiF; reduction in a Ta-vessel under Ar, start of react. at 700°C, cooling within 2-3h, removal of excess Li with H2O, mechanical separation of LiF;; |
Conditions | Yield |
---|---|
In neat (no solvent) annealing mixture of fluorides in sealed platinum tube at 1500 K for 2 d; quenching from 1300 K; X-ray powder diffraction (comparison with reported data);; |
Conditions | Yield |
---|---|
In neat (no solvent) 975.-+.25°C, streaming H2O-vapor, 4-30min; increase of react.-rate in presence of U3O8 and/or Cr2O3;; | >99 |
In neat (no solvent) 975.-+.25°C, streaming H2O-vapor, 4-30min; increase of react.-rate in presence of U3O8 and/or Cr2O3;; | >99 |
Conditions | Yield |
---|---|
In neat (no solvent) annealing calcd. amounts at 1000°C in a closed vessel, cooling slowly to 650°C;; |
xenon difluoride
ytterbium(III) fluoride
terbium(III) fluoride
terbium tetrafluoride
Conditions | Yield |
---|---|
In neat (no solvent) byproducts: Xe; heating (430-470°C, 0.5-1 h); DTA; |
Conditions | Yield |
---|---|
In diethyl ether pptn., exothermic react.;; | |
In diethyl ether pptn., exothermic react.;; |
Conditions | Yield |
---|---|
In sulfuric acid aq. H2SO4; on dissolving in satd. aq. K2SO4*Al2(SO4)3*24H2O (in presence of 1n H2SO4);; |
ytterbium(III) fluoride
potassium
Conditions | Yield |
---|---|
In neat (no solvent) |
ytterbium(III) fluoride
molybdenum(V) fluoride
molybdenum
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) byproducts: MoF3; at 260°C; impurities of MoF3 and YbF3; |
Conditions | Yield |
---|---|
In gas at high temp. at 1E-4 atm in a Ta-or graphite-Knudsen-cell;; | |
In neat (no solvent) reduction with metal-vapor at 1E-4 to 1E-5Torr, 700-950°C, Mo-apparatus;; | |
In neat (no solvent) reduction with metal-vapor at 1E-4 to 1E-5Torr, 700-950°C, Mo-apparatus;; | |
In neat (no solvent) reduction of YbF3 with Yb (molar ratio=2:1);; | |
With H2SO4 mixt. (multiple metal excess) subjecting to shock loading (cast TG charges (1:1), cylindrical container, pressure of ca. 200 kbar, residual temp. ca. 1000°C), excess metal removal (dil. sulphuric acid); |
The Ytterbium fluoride is an organic compound with the formula F3Yb. The systematic name of this chemical is ytterbium(3+) trifluoride . With the CAS registry number 13760-80-0, it is also named as ytterbium trifluoride. The product's categories are Catalysis and Inorganic Chemistry; Chemical Synthesis; Crystal Grade Inorganics; Salts; Ytterbium Salts; YtterbiumMetal and Ceramic Science. Besides, it is a white to off-white powder, which should be stored in a closed cool and well-ventilated place.
Preparation: this chemical can be prepared by HF.
When you are using this chemical, please be cautious about it as the following:
It is toxic by inhalation, in contact with skin and if swallowed. In case of contact with eyes, rinse immediately with plenty of water and seek medical advice. Besides, this chemical contacts with acids liberates very toxic gas. When you are using it, wear suitable gloves and eye/face protection. In case of accident or if you feel unwell seek medical advice immediately (show the label where possible).
You can still convert the following datas into molecular structure:
(1)SMILES: F[Yb](F)F
(2)InChI: InChI=1/3FH.Yb/h3*1H;/q;;;+3/p-3
(3)InChIKey: XASAPYQVQBKMIN-DFZHHIFOAQ
(4)Std. InChI: InChI=1S/3FH.Yb/h3*1H;/q;;;+3/p-3
(5)Std. InChIKey: XASAPYQVQBKMIN-UHFFFAOYSA-K
The toxicity data is as follows:
Organism | Test Type | Route | Reported Dose (Normalized Dose) | Effect | Source |
---|---|---|---|---|---|
mammal (species unspecified) | LDLo | intraperitoneal | 10mg/kg (10mg/kg) | Meditsina Truda i Promyshlennaya Ekologiya. Industrial Medicine and Ecology. Vol. (7), Pg. 32, 1994. |
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