Difference between revisions of "Bromite"
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| StdInChIKey = DKSMCEUSSQTGBK-UHFFFAOYSA-M | | StdInChIKey = DKSMCEUSSQTGBK-UHFFFAOYSA-M | ||
| CASNo = | | CASNo = | ||
+ | }} | ||
+ | | Section3 = {{Chembox Structure | ||
+ | | Reference = <ref>{{citation | first1 = William | last1 = Levason | first2 = J. Steven | last2 = Ogden | first3 = Mark D. | last3 = Spicer | first4 = Nigel A. | last4 = Young | title = Characterisation of the oxo-anions of bromine BrO<sub>''x''</sub><sup>−</sup> (''x'' = 1–4) by infrared, Raman, nuclear magnetic resonance, and bromine ''K''-edge extended X-ray absorption fine structure techniques | journal = J. Chem. Soc., Dalton Trans. | year = 1990 | issue = 1 | pages = 349–53 | doi = 10.1039/DT9900000349}}.</ref> | ||
+ | | MolShape = ''r''(Br–O) = 172 pm | ||
+ | }} | ||
+ | | Section4 = {{Chembox Thermochemistry | ||
+ | | Reference = <ref>{{citation | first1 = C. L. | last1 = Lee | first2 = M. W. | last2 = Lister | title = The Decomposition of Aqueous Sodium Bromite | journal = Can. J. Chem. | volume = 49 | issue = 17 | pages = 2822–26 | year = 1971 | doi = 10.1139/v71-470}}.</ref> | ||
+ | | DeltaHf = −37.2 kJ mol<sup>−1</sup> (aq) | ||
+ | | DeltaGf = +27.2 kJ mol<sup>−1</sup> (aq) | ||
+ | | Entropy = 127 J K<sup>−1</sup> mol<sup>−1</sup> (aq) | ||
}} | }} | ||
| Section8 = {{Chembox Related | | Section8 = {{Chembox Related | ||
− | | OtherAnions = [[Chlorite]] | + | | OtherAnions = [[Chlorite]]<br/><hr/>[[Hypobromite]]<br/>[[Bromate]]<br/>[[Perbromate]] |
}} | }} | ||
}} | }} | ||
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===References=== | ===References=== | ||
{{reflist}} | {{reflist}} | ||
+ | |||
+ | ===Further reading=== | ||
+ | *{{citation | title = The Decomposition of Hypobromite and Bromite Solutions | first1 = P. | last1 = Engel | first2 = A. | last2 = Oplatka | first3 = B. | last3 = Perlmutter-Hayman | journal = J. Am. Chem. Soc. | year = 1954 | volume = 76 | issue = 7 | pages = 2010–15 | doi = 10.1021/ja01636a092}}. | ||
+ | *{{citation | title = Characterization of sodium bromite by x-ray crystallography and bromine K-edge EXAFS, IR, Raman, and NMR spectroscopies | first1 = William | last1 = Levason | first2 = J. Steven | last2 = Ogden | first3 = Mark D. | last3 = Spicer | first4 = Michael | last4 = Webster | first5 = Nigel A. | last5 = Young | journal = J. Am. Chem. Soc. | year = 1989 | volume = 111 | issue = 16 | pages = 6210–12 | doi = 10.1021/ja00198a035}}. | ||
+ | *{{citation | inventor1-last = Breiss | inventor1-first = Jean | inventor2-last = Kirchner | inventor2-first = René | inventor3-last = Zimmermann | inventor3-first = Jean-Pierre | assignee = Société d'Etudes Chimiques pour l'Industrie et l'Agriculture | title = Procédé de préparation des bromites alcalins et alcalino-terreux | country-code = FR | patent-number = 1315034 | publication-date = 1963-01-18}}; {{USpatent | title = Method for preparing alkali metal and alkaline earth metal bromites | number = 3223477}}. | ||
+ | *{{citation | inventor1-last = Kircher | inventor1-first = René | inventor2-last = Périat | inventor2-first = Robert | assignee = Société d'Etudes Chimiques pour l'Industrie et l'Agriculture | title = Process for producing alkaline earth metal bromites | country-code = US | patent-number = 3095267 | publication-date = 1963-06-25}}. | ||
[[Category:Bromites| ]] | [[Category:Bromites| ]] |
Latest revision as of 07:28, 5 January 2011
Bromite | |
---|---|
Other names | Dioxidobromate(1−) |
Identifiers | |
InChI | InChI=1/BrHO2/c2-1-3/h(H,2,3)/p-1 |
InChIKey | DKSMCEUSSQTGBK-REWHXWOFAW |
Standard InChI | InChI=1S/BrHO2/c2-1-3/h(H,2,3)/p-1 |
Standard InChIKey | DKSMCEUSSQTGBK-UHFFFAOYSA-M |
ChemSpider | |
Structure[1] | |
Molecular geometry | r(Br–O) = 172 pm |
Thermochemistry[2] | |
Std enthalpy of formation ΔfH |
−37.2 kJ mol−1 (aq) |
Std Gibbs energy of formation ΔfG |
+27.2 kJ mol−1 (aq) |
Standard molar entropy S |
127 J K−1 mol−1 (aq) |
Related compounds | |
Other anions | Chlorite Hypobromite Bromate Perbromate |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
A bromite is a compound containing the dioxidobromate(1−) anion BrO−2. Bromites are formally salts of bromous acid.
Notes and references
Notes
References
- ↑ Levason, William; Ogden, J. Steven; Spicer, Mark D.; Young, Nigel A. Characterisation of the oxo-anions of bromine BrOx− (x = 1–4) by infrared, Raman, nuclear magnetic resonance, and bromine K-edge extended X-ray absorption fine structure techniques. J. Chem. Soc., Dalton Trans. 1990 (1), 349–53. DOI: 10.1039/DT9900000349.
- ↑ Lee, C. L.; Lister, M. W. The Decomposition of Aqueous Sodium Bromite. Can. J. Chem. 1971, 49 (17), 2822–26. DOI: 10.1139/v71-470.
Further reading
- Engel, P.; Oplatka, A.; Perlmutter-Hayman, B. The Decomposition of Hypobromite and Bromite Solutions. J. Am. Chem. Soc. 1954, 76 (7), 2010–15. DOI: 10.1021/ja01636a092.
- Levason, William; Ogden, J. Steven; Spicer, Mark D.; Webster, Michael; Young, Nigel A. Characterization of sodium bromite by x-ray crystallography and bromine K-edge EXAFS, IR, Raman, and NMR spectroscopies. J. Am. Chem. Soc. 1989, 111 (16), 6210–12. DOI: 10.1021/ja00198a035.
- Breiss, Jean; Kirchner, René; Zimmermann, Jean-Pierre (Société d'Etudes Chimiques pour l'Industrie et l'Agriculture) Procédé de préparation des bromites alcalins et alcalino-terreux. FR Patent 1315034, published 18 January 1963; Method for preparing alkali metal and alkaline earth metal bromites. US Patent 3223477.
- Kircher, René; Périat, Robert (Société d'Etudes Chimiques pour l'Industrie et l'Agriculture) Process for producing alkaline earth metal bromites. US Patent 3095267, published 25 June 1963.
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