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Oxide Telluride

A brief note lacking details claims the preparation of carbon oxide telluride in very low yields by the action of carbon monoxide on tellurium. Carbon oxide telluride is a gas at room temperature1. [Pg.522]

Carbon Oxid Telluride/Sulfid Telluride/Selenid Telluride etc. [Pg.523]

Tellurium formed by irradiation of uranium with thermal neutrons may have reacted with carbon monoxide to give carbon oxide telluride. ... [Pg.522]

Monolayers can be transferred onto many different substrates. Most LB depositions have been perfonned onto hydrophilic substrates, where monolayers are transferred when pulling tire substrate out from tire subphase. Transparent hydrophilic substrates such as glass [18,19] or quartz [20] allow spectra to be recorded in transmission mode. Examples of otlier hydrophilic substrates are aluminium [21, 22, 23 and 24], cliromium [9, 25] or tin [26], all in their oxidized state. The substrate most often used today is silicon wafer. Gold does not establish an oxide layer and is tlierefore used chiefly for reflection studies. Also used are silver [27], gallium arsenide [27, 28] or cadmium telluride wafer [28] following special treatment. [Pg.2614]

Heavy water, see Hydrogen[ H] oxide Heazlewoodite, see rn-Nickel disulfide Hematite, see Iron(III) oxide Hermannite, see Manganese silicate Hessite, see Silver telluride Hieratite, see Potassium hexafluorosilicate Hydroazoic acid, see Hydrogen azide Hydrophilite, see Calcium chloride Hydrosulfite, see Sodium dithionate(III)... [Pg.274]

Biphenyl Bismuth telluride Boron oxide Boron trifluoride Bromine... [Pg.373]

No other oxide phases below MO2 have been established but a yellow hydroxide , precipitated by alkali from aqueous solutions of chromium(II), spontaneously evolves H2 and forms a chromium(III) species of uncertain composition. The sulfides, selenides and tellurides of this triad are considered on p. 1017. [Pg.1009]

The heterocyclic telluride 32 is susceptible to oxidation-addition reactions and readily adds halogen atoms under a treatment with halogens or sulfuryl chloride (93MI1). Compounds 34 were obtained in almost quantitative yields. [Pg.15]

Molybdenum hexafluoride. 3,1412 Molybdenum-iron-sulfur complexes, 4,241 Molybdenum oxide amino acid formation prebiotic systems, 6, 872 Molybdenum storage protein microorganisms, 6, 681 Molybdenum telluride, 3, 1431 Molybdenum tetraalkoxides physical properties, 2, 347 Molybdenum tribromide, 3,1330 Molybdenum trichloride, 3,1330 Molybdenum trifluoride, 3, 1330 Molybdenum trihalides, 3, 1330 bond lengths, 3, 1330 magnetic moments, 3,1330 preparation, 3,1330 properties, 3, 1330 structure, 3,1330 Molybdenum triiodide, 3,1330 Molybdenum trioxide complexes, 3, 1379 Molybdenum triselenide, 3, 143)... [Pg.170]

The Alkaline-Earth Oxides, etc.—The observed and calculated inter-atomic distances for the alkaline-earth oxides, sulfides, selenides and tellurides are given in Table VIII. Except for the magnesium com-... [Pg.267]

It is also shown that theoretically a binary compound should have the sphalerite or wurzite structure instead of the sodium chloride structure if the radius ratio is less than 0.33. The oxide, sulfide, selenide and telluride of beryllium conform to this requirement, and are to be considered as ionic crystals. It is found, however, that such tetrahedral crystals are particularly apt to show deformation, and it is suggested that this is a tendency of the anion to share an electron pair with each cation. [Pg.281]

Selenic acid, H2Se04, is a strong acid (/fai 2) and the solubility of its salts parallels that of the corresponding sulfates. It is formed by the oxidation of selenous acid or elemental selenium with strong oxidizing agents in the presence of water. Telluric acid, H2Te04, or tellurates are obtained by oxidation of tellurides,... [Pg.13]

All the dialkali monosulfides are soluble in water and give alkaline solutions. The tellurides are instantly decomposed by air. They are soluble in water, but the solutions are easily oxidized to red polytellurides. The alkali metal tellurides are strong reducing agents which reduce tellurites to metallic tellurium. [Pg.28]


See other pages where Oxide Telluride is mentioned: [Pg.121]    [Pg.105]    [Pg.522]    [Pg.121]    [Pg.522]    [Pg.121]    [Pg.105]    [Pg.522]    [Pg.121]    [Pg.522]    [Pg.386]    [Pg.273]    [Pg.166]    [Pg.118]    [Pg.84]    [Pg.581]    [Pg.754]    [Pg.766]    [Pg.767]    [Pg.781]    [Pg.77]    [Pg.82]    [Pg.134]    [Pg.147]    [Pg.155]    [Pg.173]    [Pg.232]    [Pg.236]    [Pg.278]    [Pg.281]    [Pg.155]    [Pg.251]    [Pg.4]    [Pg.12]    [Pg.71]    [Pg.72]   
See also in sourсe #XX -- [ Pg.3 , Pg.4 , Pg.10 ]




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Carbon Oxide Telluride

Oxidation of diaryl tellurides

Oxides, Sulphides, and Tellurides

Tellurides

Tellurides oxidation

The Alkaline-Earth Oxides, Sulfides, Selenides, and Tellurides

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