Tellurite tellurate explained

A tellurite tellurate is chemical compound or salt that contains tellurite and tellurate anions [TeO<sub>3</sub>]2- [TeO<sub>4</sub> ]2-. These are mixed anion compounds, meaning the compounds are cations that contain one or more anions. Some have third anions. Environmentally, tellurite [TeO<sub>3</sub>]2- is the more abundant anion due to tellurate's [TeO<sub>4</sub> ]2- low solubility limiting its concentration in biospheric waters. Another way to refer to the anions is tellurium's oxyanions, which happen to be relatively stable.

Naming

A tellurite tellurate compound may also be called a tellurate tellurite. Compounds that contain the anions follow basic nomenclature rules, the cation is named first, followed by the anion. As individual ions current IUPAC naming conventions dictate that compounds containing what was conventionally known as the tellurite ion, [TeO<sub>3</sub>]2-, be named as tellurate (IV) compounds, while other tellurates are labeled tellurate (VI) compounds. Furthering confusion, a number of other tellurate oxyanions exist, including pentoxotellurate, [TeO<sub>5</sub>]4-, and ditellurate, [Te<sub>2</sub>O<sub>10</sub>]8-. Additionally, a number of compounds that do not even include tellurium oxyanions still have "tellurate" in their names, as in the case of octafluoridotellurate, [TeF<sub>8</sub>]2-.

Production

One way to produce a tellurite tellurate compound is by heating oxides together. Tellurite tellurate compounds can also occur naturally as minerals such as Carlfriesite Ca[Te<sup>4+</sup><sub>2</sub>Te<sup>6+</sup>O<sub>8</sub>].

Properties

Tellurite tellurate compounds can crystalize under certain conditions. Monoclinic and orthorhombic dominate crystal structures of the tellurite tellurates. Most compounds are transparent from near ultraviolet to the near infrared. Te-O bonds cause absorption lines in infrared. Sodium tellurite exhibit

Related

Related to these are the selenate selenites and sulfate sulfites by varying the chalcogen.

List

nameformularatioTeO3:TeO4mwsystemspace groupunit cell Åvolumedensityopticalreferences
NH4Te2O5(OH)1:1370.24orthorhombicPnmaa=7.340 b=5.546 c=13.164 Z=4535.94.50[1]
K2Te4O121:3780.59monoclinicC2/ma=12.360 b=7.248 c=11.967 β =105.68 Z=41032.25.03[2] [3]
K4[Te<sub>5</sub><sup>6+</sup>Te<sub>3</sub><sup>4+</sup>]O233:51545.18orthorhombicPna21a = 19.793, b = 14.664, c = 7.292, Z = 4[4]
CarlfriesiteCa[Te<sup>4+</sup><sub>2</sub>Te<sup>6+</sup>O<sub>8</sub>]2:1550.87monoclinicC2/ca=12.576 b=5.662 c=9.884 β=115.566.3
K4V6[Te<sub>2</sub><sup>4+</sup>Te<sup>6+</sup>]O242:11228.83trigonalRca = 9.7075, c = 42.701, Z = 63484.9[5]
Co2+6(Te6+O6)(Te4+O3)2Cl22:1999.30tetragonalP42/mbca = 8.59 c = 5.91 [6]
Rb4[Te<sub>5</sub><sup>6+</sup>Te<sub>3</sub><sup>4+</sup>]O233:51730.66orthorhombicPna21a = 19.573, b = 14.448, c = 7.273, Z = 4
Rb4V6[Te<sub>2</sub><sup>4+</sup>Te<sup>6+</sup>]O242:11414.31trigonalRca = 9.8399, c = 43.012, Z = 63606.6
Sr[Te<sup>4+</sup><sub>2</sub>Te<sup>6+</sup>O<sub>8</sub>] 2:1598.42tetragonalP42/ma=6.8321 c=6.7605
SrCuTe2O71:1518.36orthorhombicPbcma = 7.1464, b = 15.061, c = 5.4380, Z = 4585.3[7]
NaYTe2O71:1479.10monoclinicP21/na=6.7527 b=7.5077 c=11.8867 β =99.935 Z=4593.595.361[8]
RbTe1·25Mo0·75O6a=10.469[9]
(Ag,Na)2Te4O15 x=0.42:2monoclinicP21/ca = 6.333, b = 24.681, c = 7.308, β = 110.84° Z = 4
Ag2[Te<sup>4+</sup>Te<sup>6+</sup>O<sub>6</sub>]1:1566.93monoclinicP21/m a=5.4562 b=7.4009 c=6.9122 β=101.237
Ag2[Te<sup>4+</sup><sub>2</sub>Te<sup>6+</sup><sub>2</sub>O<sub>11</sub>]2:2902.13triclinicPa=7.287 b=7.388 c=9.686 α=95.67 β=94.10 γ=119.40
Cd2Te4+Te6+O71:1592.02monoclinicP21/ca=9.3039 b=7.3196 c=13.2479 β=122.914
Cs2Te4+Te36+O121:3968.20rhombohedralRma=7.2921 c=18.332[10]
CsTe2O6–x1:1484.10cubic
CsTe2O6–x1:1484.10orthorhombic
BaTe2O61:1488.52orthorhombicCmcma=5.569 b=12,796 c=7.320 Z=46.19[11]
BaMgTe2O71:1528.83orthorhombicAma2a = 5.558, b = 15.215, c = 7.307 Z = 4617.9SHG 5 × KDP[12]
CsTe1·13Mo0·864O6a=10.643
BaCoTeO3TeO41:1563.46orthorhombicAma2[13]
BaCuTeO3TeO41:1568.07orthorhombicAma2a = 5.4869, b =15.412, c = 7.2066, Z = 4.609.42[14]
BaZnTe2O7569.91orthorhombicAma2a = 5.5498, b = 15.316, c = 7.3098, Z = 4621.34SHG 5 × KDP
CeV3Te3O15(OH)3·2H2O995.74hexagonalP63/mmca=12.166 c=12.537 Z=41606.94.116dark red[15]
PrV3Te3O15(OH)3·2H2O996.53hexagonalP63/mmca=12.1147 c=12.4949 Z=41588.14.168dark red
NdV3Te3O15(OH)3·H2O983.86hexagonalP63/mmca=12.1075 c=12.4572 Z=41581.54.132dark red
SmV3Te3O15(OH)3·H2O989.97hexagonalP63/mmca=12.1068 c=12.4509 Z=41580.54.160dark red
EuV3Te3O15(OH)3·H2O991.58hexagonalP63/mmca=12.0731 c=12.3674 Z=41561.24.219dark red
GdV3Te3O15(OH)3·H2O996.87hexagonalP63/mmca=12.0745 c=12.3701 Z=41561.94.239dark red
RbTe1·5W0·5O6a=10.462
CsTe1·625W0·375O6a=10.543
α-Hg2Te2O71:1768.38monoclinicC2/ca=12.910 b=7.407 c=13.256 β =112.044 Z=8[16]
β-Hg2Te2O71:1768.38orthorhombicAea2a=7.441, b=23.713,c=13.522, Z=16
PbCuTe2O71:1637.94orthorhombicPbcma = 7.2033, b = 15.047, c = 5.4691, Z = 4592.78
Bi[(Bi<sup>3+</sup>Te<sup>4+</sup>)Te<sup>6+</sup>O<sub>8</sub>]801.16
(Ca,Pb)3CaCu6[Te<sup>4+</sup><sub>3</sub>Te<sup>6+</sup>O<sub>12</sub>]2(Te4+O3)2(SO4)2 3111.30trigonalP3 2 1a=9.1219(17), c=11.9320(9)4.65Viridian green[17]

Notes and References

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  2. Loeksmanto. Waloejo. Moret. Jacques. Maurin. Maurice. Philippot. Etienne. July 1980. Etude cristallochimique comparée et conductivité électrique de deux tellurates mixtes: AgxNa2−xTe2IVTe3VIO14 (x = 0,4) et K2TeIVTe3VIO12. Journal of Solid State Chemistry. fr. 33. 2. 209–217. 10.1016/0022-4596(80)90122-X.
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  17. https://www.mindat.org/min-3983.html