Difference between revisions of "Caesium hydroxide"
Physchim62 (talk | contribs) |
Physchim62 (talk | contribs) (safety data) |
||
Line 32: | Line 32: | ||
}} | }} | ||
| Section7 = {{Chembox Hazards | | Section7 = {{Chembox Hazards | ||
+ | | Reference <ref>{{GHS class JP|id=812|accessdate=2009-08-26}}.</ref> | ||
| ExternalMSDS = {{ICSC-small|15|92}} | | ExternalMSDS = {{ICSC-small|15|92}} | ||
| EUIndex = not listed | | EUIndex = not listed | ||
+ | | GHSPictograms = {{GHS skull and crossbones|Acute Tox. (inhal.) 1}}{{GHS corrosion|Skin Corr. 1B, Eye Dam. 1}}{{GHS exclamation mark|Acute Tox. (oral) 4}} | ||
+ | | GHSSignalWord = DANGER | ||
+ | | HPhrases = {{H-phrases|330|314|318|302}} | ||
| FlashPt = non-flammable | | FlashPt = non-flammable | ||
}} | }} |
Revision as of 20:13, 25 August 2009
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
|
Caesium hydroxide (CsOH) is a chemical compound consisting of an atom of caesium and a hydroxide group (also known as hydroxyl). It is a powerful base, much like other alkali metal hydroxides such as sodium hydroxide and potassium hydroxide. In fact, caesium hydroxide is powerful enough to quickly corrode through glass.
Due to its high reactivity, caesium hydroxide is extremely hygroscopic. Laboratory caesium hydoxide is typically a hydrate.
It is an anisotropic etchant of silicon, exposing octahedral planes. This technique can create pyramids and regularly-shaped etch pits for uses such as MEMS. It is known to have a higher selectivity to etch highly p-doped silicon than the more commonly used potassium hydroxide.[ref. needed]
However, this compound is not usually used in experiments as the extraction of caesium is very expensive and the fact that it behaves very much like rubidium hydroxide and potassium hydroxide but reacts chemically stronger than they do.
Caesium hydroxide can be obtained by the following chemical reaction:
- 2Cs + 2H2O → 2CsOH + H2
The above reaction occurs explosively with enough force to shatter a Pyrex beaker.
References
Further reading
- Corey, E. J.; Noe, Mark C. Preparation of O-Allyl-N-(9-anthracenylmethyl)cinchonidinium Bromide as a Phase Transfer Catalyst for the Enantioselective Alkylation of Glycine Benzophenone Imine tert-Butyl Ester: (4S)-2-(Benzhydrylidenamino)pentanedioic Acid, 1-tert-Butyl Ester-5-Methyl Ester. Org. Synth. 2003, 80, 38, <http://www.orgsyn.org/orgsyn/orgsyn/prepContent.asp?prep=v80p0038>.
External links
Error creating thumbnail: Unable to save thumbnail to destination | This page was originally imported from Wikipedia, specifically this version of the article "Caesium hydroxide". Please see the history page on Wikipedia for the original authors. This WikiChem article may have been modified since it was imported. It is licensed under the Creative Commons Attribution–Share Alike 3.0 Unported license. |