Tin(IV) iodide: Difference between revisions
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'''Tin(IV) iodide''', also known as '''stannic iodide''' is the [[chemical compound]] with the [[chemical formula|formula]] SnI<sub>4</sub>. This tetrahedral molecule crystallises as a bright orange solid that dissolves readily in nonpolar solvents such as [[benzene]].<ref>[http://www.webelements.com/webelements/compounds/text/Sn/I4Sn1-7790478.html Chemistry : Periodic Table : tin : compound data [tin (IV) iodide]<!-- Bot generated title -->]</ref> |
'''Tin(IV) iodide''', also known as '''stannic iodide''' is the [[chemical compound]] with the [[chemical formula|formula]] SnI<sub>4</sub>. This tetrahedral molecule crystallises as a bright orange solid that dissolves readily in nonpolar solvents such as [[benzene]].<ref>[http://www.webelements.com/webelements/compounds/text/Sn/I4Sn1-7790478.html Chemistry : Periodic Table : tin : compound data [tin (IV) iodide]<!-- Bot generated title -->]</ref> |
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The compound is usually prepared by the reaction of [[iodine]] and tin:<ref name=Moeller>{{cite journal |author= Moeller, T., Edwards, D. C., Brandt, R. L. and Kleinberg, J. |title= Tin(IV) Iodide (Stannic Iodide) |journal= [[Inorganic Syntheses]] |year= 1953 |volume= 4 |pages= 119–121 |doi= 10.1002/9780470132357.ch40 |series= Inorganic Syntheses |isbn= |
The compound is usually prepared by the reaction of [[iodine]] and tin:<ref name=Moeller>{{cite journal |author= Moeller, T., Edwards, D. C., Brandt, R. L. and Kleinberg, J. |title= Tin(IV) Iodide (Stannic Iodide) |journal= [[Inorganic Syntheses]] |year= 1953 |volume= 4 |pages= 119–121 |doi= 10.1002/9780470132357.ch40 |series= Inorganic Syntheses |isbn= 978-0-470-13235-7 }}</ref> |
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:[[tin|Sn]] + 2 [[iodine|I<sub>2</sub>]] → SnI<sub>4</sub> |
:[[tin|Sn]] + 2 [[iodine|I<sub>2</sub>]] → SnI<sub>4</sub> |
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The compound [[hydrolysis|hydrolyses]] in water.<ref>{{cite journal |journal= J. Chem. Educ. |author= Hickling, G. G. |title= Gravimetric analysis: The synthesis of tin iodide |year= 1990 |volume= 67 |issue= 8 |pages= 702–703 |doi= 10.1021/ed067p702 }}</ref> In aqueous [[hydroiodic acid]], it reacts to form a rare example of a metal hexaiodide:<ref name=Moeller/> |
The compound [[hydrolysis|hydrolyses]] in water.<ref>{{cite journal |journal= J. Chem. Educ. |author= Hickling, G. G. |title= Gravimetric analysis: The synthesis of tin iodide |year= 1990 |volume= 67 |issue= 8 |pages= 702–703 |doi= 10.1021/ed067p702 }}</ref> In aqueous [[hydroiodic acid]], it reacts to form a rare example of a metal hexaiodide:<ref name=Moeller/> |
Revision as of 23:07, 5 May 2012
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Names | |||
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IUPAC name
tin(IV) iodide
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Other names
tin tetraiodide
stannic iodide | |||
Properties | |||
SnI4 | |||
Molar mass | 626.328 g mol−1 | ||
Appearance | red-orange solid | ||
Density | 4.56 g cm−3 | ||
Melting point | 144 °C[1] | ||
Boiling point | 348 °C | ||
Structure | |||
Cubic, cP40 | |||
P-43m, No. 205 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tin(IV) iodide, also known as stannic iodide is the chemical compound with the formula SnI4. This tetrahedral molecule crystallises as a bright orange solid that dissolves readily in nonpolar solvents such as benzene.[2]
The compound is usually prepared by the reaction of iodine and tin:[3]
The compound hydrolyses in water.[4] In aqueous hydroiodic acid, it reacts to form a rare example of a metal hexaiodide:[3]
- SnI4 + 2 I− → [SnI6]2−
Related pages
References
- ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
- ^ Chemistry : Periodic Table : tin : compound data [tin (IV) iodide]
- ^ a b Moeller, T., Edwards, D. C., Brandt, R. L. and Kleinberg, J. (1953). "Tin(IV) Iodide (Stannic Iodide)". Inorganic Syntheses. Inorganic Syntheses. 4: 119–121. doi:10.1002/9780470132357.ch40. ISBN 978-0-470-13235-7.
{{cite journal}}
: CS1 maint: multiple names: authors list (link) - ^ Hickling, G. G. (1990). "Gravimetric analysis: The synthesis of tin iodide". J. Chem. Educ. 67 (8): 702–703. doi:10.1021/ed067p702.