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{{chembox {{chembox
| Watchedfields = changed
| verifiedrevid = 399519221
| ImageFile = Ammonium perrhenate.png | verifiedrevid = 419461299
| ImageFile = Ammonium perrhenate.png
| ImageFile1 = Ammonium_perrhenate.jpg | ImageFile1 = Ammonium_perrhenate.jpg
<!-- | ImageSize = 250px --> <!-- | ImageSize = 250px -->
| ImageName = Ammonium perrhenate | ImageName = Ammonium perrhenate
| OtherNames = Ammonium perrhenate,<br />Ammonium perrhenate(VII) | OtherNames = Ammonium perrhenate,<br />Ammonium perrhenate(VII)
| Section1 = {{Chembox Identifiers |Section1={{Chembox Identifiers
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID = 2341271 | ChemSpiderID = 2341271
| InChI = 1/H3N.4O.Re/h1H3;;;;;/q;;;;-1;/p+1/rH3N.O4Re/c;1-5(2,3)4/h1H3;/q;-1/p+1 | InChI = 1/H3N.4O.Re/h1H3;;;;;/q;;;;-1;/p+1/rH3N.O4Re/c;1-5(2,3)4/h1H3;/q;-1/p+1
| InChIKey = HOJYZCWLNWENHS-WUACXKGRAA | InChIKey = HOJYZCWLNWENHS-WUACXKGRAA
| SMILES = (=O)(=O)=O. | SMILES = (=O)(=O)=O.
| StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/H3N.4O.Re/h1H3;;;;;/q;;;;-1;/p+1 | StdInChI = 1S/H3N.4O.Re/h1H3;;;;;/q;;;;-1;/p+1
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = HOJYZCWLNWENHS-UHFFFAOYSA-O | StdInChIKey = HOJYZCWLNWENHS-UHFFFAOYSA-O
| CASNo_Ref = {{cascite|correct|??}}
| CASNo = 13598-65-7 | CASNo = 13598-65-7
| PubChem = 3084163
| EINECS = 237-075-6
}} }}
| Section2 = {{Chembox Properties |Section2={{Chembox Properties
| Formula = NH<sub>4</sub>ReO<sub>4</sub> | Formula = NH<sub>4</sub>ReO<sub>4</sub>
| MolarMass = 268.2359 g/mol | MolarMass = 268.2359&nbsp;g/mol
| Density = 3.97 g/cm³, solid | Density = 3.97&nbsp;g/cm<sup>3</sup>, solid
| Solubility = 2.8&nbsp;g/100&nbsp;mL (0&nbsp;°C), 6.2&nbsp;g/100&nbsp;mL (20&nbsp;°C), 12.0&nbsp;g/100&nbsp;mL (40&nbsp;°C), 20.7&nbsp;g/100&nbsp;mL (60&nbsp;°C), 32.3&nbsp;g/100&nbsp;mL (80&nbsp;°C), 39.1&nbsp;g/100&nbsp;mL (90&nbsp;°C)
| Solubility = soluble.
| MeltingPt = 200°C (decomposes)<ref name="Brauer">{{Citation |last=Georg Brauer |title=Ammoniumperrhenat |date=1954 |page=1108 |publisher=Ferdinand Enke Verlag}}</ref>
| MeltingPt = °C
| BoilingPt = | BoilingPt =
}} }}
| Section3 = {{Chembox Structure |Section3={{Chembox Structure
| Coordination = N/A | Coordination = N/A
| CrystalStruct = ] | CrystalStruct = ]
}} }}
| Section7 = {{Chembox Hazards |Section7={{Chembox Hazards
| ExternalMSDS = | ExternalSDS =
| FlashPt = Non-flammable
| EUClass = Not listed.
| FlashPt = Non-flammable.
}} }}
| Section8 = {{Chembox Related |Section8={{Chembox Related
| OtherAnions = ]; ] | OtherAnions = ]; ]
| OtherCations = ]; ] | OtherCations = ]; ]
| OtherCpds = | OtherCompounds =
}} }}
}} }}
'''Ammonium perrhenate''' (APR) is the ] salt of ], NH<sub>4</sub>ReO<sub>4</sub>. This is the most common form in which ] is traded. Prices are quoted in US Dollars per kg ] content. ] content of APR is typically 69.0 - 69.4%. '''Ammonium perrhenate''' (APR) is the ] salt of ], NH<sub>4</sub>ReO<sub>4</sub>. It is the most common form in which ] is traded. It is a white salt; soluble in ethanol and water, and mildly soluble in NH<sub>4</sub>Cl.<ref name=":0">{{Cite book |last=Lidin |first=R. |title=Неорганическая химия в реакциях |publisher=Drofa |year=2007 |isbn=978-5-358-01303-2 |edition=2nd |location=Moscow |pages=332 |language=ru |trans-title=Inorganic chemistry in reactions}}</ref> It was first described soon after the discovery of rhenium.<ref>{{Cite journal |last=Noddack |first=J. |last2=Noddack |first2=W. |year=1929 |title=Die Sauerstoffverbindungen des Rheniums |trans-title=The oxygen compounds of rhenium |journal=Zeitschrift für anorganische und allgemeine Chemie |language=de |volume=181 |issue=6 |pages=1–37 |bibcode=1929NW.....17...93N |doi=10.1002/zaac.19291810102}}</ref>


==Structure== ==Structure==
] ]
The crystal structure of APR is that of ], in which the atomic cation is replaced by the ammonium molecular cation<ref name = rjcbrown>{{cite journal | journal = ] | author = I.P. Swainson and R.J.C. Brown | title = Refinement of ammonium perrhenate structure using a pseudo-spin model for the ] orientation |volume = B53| pages = 76–81 | year = 1997|doi = 10.1107/S0108768196011160}}</ref>. It undergoes a molecular orientational ordering transition on cooling without change of space group, but with a highly anisotropic change in the shape of the ], resulting in the unusual property of having a positive temperature and pressure Re ] coefficient<ref name = brown-segal>{{cite journal | journal = ] | author = R.J.C. Brown and S.L. Segel | title = <sup>187</sup>Re, <sup>14</sup>N, and <sup>2</sup>H nuclear quadrupole couplings in NH<sub>4</sub>ReO<sub>4</sub>: Evidence for a possible phase transition |volume = 67 | issue = 7| pages = 3163–7 | year = 1977|doi = 10.1063/1.435229}}</ref>. The crystal structure of APR resembles that of ], with atomic cation is replaced by ammonium. The ] (NH<sub>4</sub>TcO<sub>4</sub>), ] (NH<sub>4</sub>IO<sub>4</sub>), tetrachlorothallate (NH<sub>4</sub>TlCl<sub>4</sub>), and tetrachloroindate (NH<sub>4</sub>InCl<sub>4</sub>) follow this motif.<ref name="rjcbrown">{{cite journal |last=I. P. Swainson and R. J. C. Brown |year=1997 |title=Refinement of ammonium perrhenate structure using a pseudo-spin model for the ammonium ion orientation |journal=] |volume=B53 |issue=1 |pages=76–81 |doi=10.1107/S0108768196011160|bibcode=1997AcCrB..53...76S }}</ref> It undergoes a molecular orientational ordering transition on cooling without change of space group, but with a highly anisotropic change in the shape of the ], resulting in the unusual property of having a positive temperature and pressure Re ] coefficient.<ref name = brown-segal>{{cite journal |last=R. J. C. Brown and S. L. Segel |year=1977 |title=<sup>187</sup>Re, <sup>14</sup>N, and <sup>2</sup>H nuclear quadrupole couplings in NH<sub>4</sub>ReO<sub>4</sub>: Evidence for a possible phase transition |journal=] |volume=67 |issue=7 |pages=3163–7 |bibcode=1977JChPh..67.3163B |doi=10.1063/1.435229}}</ref> APR does not give hydrates.<ref name=":0" />

NH<sub>4</sub>ReO<sub>4</sub> can be regarded as the prototype structure of a family of ammonium scheelites, which include the ] (NH<sub>4</sub>TcO<sub>4</sub>), ] (NH<sub>4</sub>IO<sub>4</sub>), tetrachlorothallate (NH<sub>4</sub>TlCl<sub>4</sub>) and tetrachloroindate (NH<sub>4</sub>InCl<sub>4</sub>)<ref name= "rjcbrown"/>.


==Preparation== ==Preparation==
Ammonium perrhenate may be prepared from virtually all common sources of rhenium. The metal, oxides, and sulfides can be oxidized with ] and the resulting solution treated with aqueous ammonia. Alternatively an aqueous solution of Re<sub>2</sub>O<sub>7</sub> can be treated with ammonia followed by crystallisation.<ref>O. Glemser "Ammonium Perrhenate" in '''', 2nd Ed. Edited by G. Brauer, Academic Press, 1963, New York. vol. 1. p. –85.</ref><ref>{{cite book |last=Richard J. Thompson |title=Inorganic Syntheses |year=1966 |chapter=Ammonium Perrhenate |series=] |volume=8 |pages=171–173 |doi=10.1002/9780470132395.ch44 |isbn=9780470132395}}</ref>
Ammonium perrhenate may be prepared from elemental rhenium by dissolving in ammoniacal ] (also known as ]).<ref name = patnaik/>


==Reactions== ==Reactions==
Ammonium perrhenate is weak oxidizer. It slowly reacts with hydrochloric acid:<ref name=":0" />
Pure ] powder can be produced from APR by reducing it with ]:<ref name = patnaik>{{cite book | title = Handbook of Inorganic Chemicals | author = Pradyot Patnaik | publisher = ] | location = New York | isbn = 0-07-049439-8 | pages = 789–790 | year = 2003}}</ref>
:NH<sub>4</sub>ReO<sub>4</sub> + 6 HCl → NH<sub>4</sub> + Cl<sub>2</sub> + 3H<sub>2</sub>O.

It is reduced to metallic Re upon heating under ]:<ref name="Brauer" />
:2 NH<sub>4</sub>ReO<sub>4</sub> + 7 H<sub>2</sub> &rarr; 2 Re + 8 H<sub>2</sub>O + 2 NH<sub>3</sub>
:2 NH<sub>4</sub>ReO<sub>4</sub> + 7 H<sub>2</sub> → 2 Re + 8 H<sub>2</sub>O + 2 NH<sub>3</sub>
Ammonium perrhenate decomposes to volatile ] starting at 250&nbsp;°C. When heated in a sealed tube at 500&nbsp;°C, It decomposes to ]:<ref name=Brauer/>
:2NH<sub>4</sub>ReO<sub>4</sub> → 2ReO<sub>2</sub> + N<sub>2</sub> + 4 H<sub>2</sub>O
The ammonium ion can be displaced with some concentrated nitrates e.g. potassium nitrate,, silver nitrate, etc.:<ref name=":0" />
:NH<sub>4</sub>ReO<sub>4</sub> + KNO<sub>3</sub> → KReO<sub>4</sub> ↓ + NH<sub>4</sub>NO<sub>3</sub>
It can be reduced to ] with sodium in ethanol:<ref name=":0" />
:NH<sub>4</sub>ReO<sub>4</sub> + 18Na + 13C<sub>2</sub>H<sub>5</sub>OH → Na<sub>2</sub> + 13NaC<sub>2</sub>H<sub>5</sub>O + 3NaOH + NH<sub>3</sub>•H<sub>2</sub>O.


==References== ==References==
<references/> <references />
* {{cite journal |last=Wm. T. Smith, S. Harmon Long |year=1948 |title=The Salts of Perrhenic Acid. I. The Alkali Metals and Ammonium |journal=] |volume=70 |issue=1 |pages=354–356 |doi=10.1021/ja01181a110}}
* {{cite journal
| title = The Salts of Perrhenic Acid. I. The Alkali Metals and Ammonium
| author = Wm. T. Smith, S. Harmon Long
| journal = ]
| volume = 70
| issue = 1
| year = 1948
| pages = 354–356
| doi = 10.1021/ja01181a110 }}


{{Rhenium compounds}}
==Further reading==
{{Ammonium salts}}
* {{Cite journal | journal = ] | volume = 8 | pages = 171–173 | title = Ammonium Perrhenate | author = Richard J. Thompson, Tung-Ch'Ing Wang, Jacob Kleinberg, George M. Adams, Burl E. Bryant | doi = 10.1002/9780470132395.ch44 | year = 1966}}
{{Perrhenates}}


{{DEFAULTSORT:Ammonium Perrhenate}} {{DEFAULTSORT:Ammonium Perrhenate}}
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