tellurium(IV) oxide
tellurium oxide
Conditions | Yield |
---|---|
annealing at 250°C for 30 min; |
Conditions | Yield |
---|---|
In neat (no solvent) in presence of air;; | 0% |
In neat (no solvent) in presence of air;; | |
In neat (no solvent) in presence of air;; | |
In neat (no solvent) in presence of air;; | 0% |
oxygen
A
tellurium(IV) oxide
B
tellurium monoxide
D
(TeO2)2
E
tellurium oxide
Conditions | Yield |
---|---|
In solid matrix other Radiation; laser ablation of Te using Nd:YAG laser in the presence of O2 in Ar matrix - other products TeOTe, cyclic-TeTeO and O3; identified by IR; |
Conditions | Yield |
---|---|
In water on storage TeF6 over water, evaporation of the soln. and heating residue;; |
water
tellurium tetrachloride
A
tellurium(IV) oxide
B
tellurium oxide
Conditions | Yield |
---|---|
In water hydrolysis of TeCl4;; small amounts of TeO3;; | |
In water hydrolysis of TeCl4;; small amounts of TeO3;; |
Conditions | Yield |
---|---|
In not given anodic oxidation in borate- and (NH4)2HPO4-soln.;; as film on the electrode obtained;; |
boron tris{pentafluoro-oxotellurate(VI)}
B
boron trifluoride
C
tellurium oxide
D
tellurium hexafluoride
Conditions | Yield |
---|---|
decompn. above 140°C; | |
decompn. above 140°C; |
boron tris{pentafluoro-oxotellurate(VI)}
A
boron trifluoride
B
tellurium oxide
C
tellurium hexafluoride
Conditions | Yield |
---|---|
decompn. above 350°C; | |
decompn. above 350°C; |
telluric acid
tellurium oxide
Conditions | Yield |
---|---|
In neat (no solvent) heating at 330 °C for several weeks;; | |
In neat (no solvent) heating at 330 °C for several weeks;; | |
With air at 399.84℃; for 12h; |
tellurium oxide
Conditions | Yield |
---|---|
With air In neat (no solvent) on heating to 220-395°C in air;; |
C
tellurium oxide
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Cu-complex heated at 30-500°C under N2 at 5°C/min; |
B
tellurium oxide
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) Cu-complex heated at 30-500°C under N2 at 5°C/min; |
tellurium oxide
Conditions | Yield |
---|---|
at 400℃; for 12h; |
Conditions | Yield |
---|---|
In not given slow formn. of Te on boiling; |
tellurium oxide
tellurium(IV) oxide
Conditions | Yield |
---|---|
With sulfur reduction with S;; | |
In neat (no solvent) heating at 420°C;; | |
375°C; | |
In neat (no solvent) decomposition of TeO3 started at 350 °C, at 600 °C (in presence of Na2CO3 at 700 °C) total conversion;; | >99 |
tellurium oxide
Conditions | Yield |
---|---|
With sodium dithionite In water quantitative reduction of TeO3 with aq. Na2S2O4;; | >99 |
With sodium dithionite In water quantitative reduction of TeO3 with an excess of Na2S2O4 in alkaline soln.;; | >99 |
With Na2S2O4 In water quantitative reduction of TeO3 with an excess of Na2S2O4 in alkaline soln.;; | >99 |
With Na2S2O4 In water quantitative reduction of TeO3 with aq. Na2S2O4;; | >99 |
With Na2S2O4 In water |
Conditions | Yield |
---|---|
In neat (no solvent) stoichiometric amounts of LiCO3 and TeO3 were heated in O2 or air at 400 and 550 °C for 24h each;; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) temp. gradually raising (20°C to 700°C, 100 K every 4 h, ratio 1:1:1); X-ray diffraction; |
Conditions | Yield |
---|---|
In water satn. of an aq. soln. of TeO3 and MoO3 (1:4) with NH3;; crystn.; washing with alc. and ether;; | |
In water satn. of an aq. soln. of TeO3 and MoO3 (1:4) with NH3;; crystn.; washing with alc. and ether;; |
Conditions | Yield |
---|---|
In neat (no solvent) heating (700-800°C, closed Au- or Ag-tubes); |
tellurium(IV) oxide
tellurium oxide
Conditions | Yield |
---|---|
With CsCl In neat (no solvent, solid phase) mixt. of lanthanide oxide, TeO2 and TeO3 in molar ratio 1:7:1 and fiveteenfold excess of CsCl (flux) heated in evacuated quartz ampoule at 750°C for 5 h; cooled to 500°C and held at this temp. for 4 d then tempered at 750°C for 4 d; |
tellurium oxide
Conditions | Yield |
---|---|
In water cooling or evapn. of aq. K2Cr2O7/TeO3/CrO3 soln. (mole ratio 1:1:2); crystn.;; | |
In water cooling or evapn. of aq. K2Cr2O7/TeO3/CrO3 soln. (mole ratio 1:1:2); crystn.;; |
Conditions | Yield |
---|---|
With hydrogen fluoride In water molar ratio TeO2:KOH=1:2 ; evaporating, mixed with 40% HF, cooling; | |
With HF In water molar ratio TeO2:KOH=1:2 ; evaporating, mixed with 40% HF, cooling; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) temp. gradually raising (20°C to 700°C, 100 K every 4 h, ratio 1:1:1); X-ray diffraction; |
Conditions | Yield |
---|---|
With KNO3 In neat (no solvent, solid phase) temp. gradually raising (20°C to 700°C, 100 K every 4 h, ratio 1:1:1); X-ray diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent, solid phase) temp. gradually raising (20°C to 700°C, 100 K every 4 h, ratio 1:1:1); X-ray diffraction; |
Conditions | Yield |
---|---|
In neat (no solvent) heating (700-800°C, closed Au- or Ag-tubes); |
Conditions | Yield |
---|---|
In neat (no solvent) tempering (ratio K:Li:Te 1:6:1, 740°C, 30 d, Ag-tube); |
The Tellurium oxide, with CAS registry number 13451-18-8, has the systematic name of oxotellane dioxide. This chemical is an inorganic chemical compound of tellurium and oxygen. And the Tellurium oxide has two forms: α-TeO3 and β-TeO3. The α-TeO3 is yellow-red and the other one is grey, rhombohedral. What's more, its EINECS is 231-193-1.
Physical properties of Tellurium oxide: (1)#H bond acceptors: 3; (2)#H bond donors: 0; (3)#Freely Rotating Bonds: 0; (4)Polar Surface Area: 51.21 Å2.
There are two differents ways of preparation about the two forms: α-TeO3 and β-TeO3. The α-TeO3 can be prepared by heating orthotelluric acid, Te(OH)6 at over 300°C . The β-TeO3 form can be prepared by heating α-TeO3 in a sealed tube with O2 and H2SO4.
You can still convert the following datas into molecular structure:
(1)SMILES: O=[Te](=O)=O
(2)InChI: InChI=1/O3Te/c1-4(2)3
(3)InChIKey: IIXQANVWKBCLEB-UHFFFAOYAH
(4)Std. InChI: InChI=1S/O3Te/c1-4(2)3
(5)Std. InChIKey: IIXQANVWKBCLEB-UHFFFAOYSA-N
About|Contact|Cas|Product Name|Molecular|Country|Encyclopedia
Message|New Cas|MSDS|Service|Advertisement|CAS DataBase|Article Data|Manufacturers | Chemical Catalog
©2008 LookChem.com,License: ICP
NO.:Zhejiang16009103
complaints:service@lookchem.com Desktop View