docberto
Harmless
Posts: 20
Registered: 29-5-2005
Member Is Offline
Mood: No Mood
|
|
Ionic liquid
I have just received some cetylpyridinium bromide. Its melting point is around 80C, making it an "ionic liquid." Does anyone have any
suggestions of what to use this solvent for? I have been considering it to electrolyze a sodium salt. Would the sodium and/or a halogen attack this
solvent? I can't think of anything, but there might be something I'm forgetting. Are there any cool reactions that require ionic solvents?
|
|
sparkgap
International Hazard
Posts: 1234
Registered: 16-1-2005
Location: not where you think
Member Is Offline
Mood: chaotropic
|
|
Googling around says it's a "quat" (that's quaternary ammonium compound to 'ya...) that is used as a surfactant and
antiseptic...
Maybe you can try if it can be used as a PTC?
sparky (~_~)
"What's UTFSE? I keep hearing about it, but I can't be arsed to search for the answer..."
|
|
mykhal
Harmless
Posts: 23
Registered: 4-4-2003
Member Is Offline
Mood: No Mood
|
|
There's a nice book on this topic, look at Amazon. A copy of it in djvu format appears somewhere on the web. If you can't find it, I can upload it to axehandle's ftp as soon as I
obtain an account.
|
|
docberto
Harmless
Posts: 20
Registered: 29-5-2005
Member Is Offline
Mood: No Mood
|
|
Yes, it is a quat. Most of the ionic liquids I can think of (imidazoliums, pyrdiniums, tetralkoniums) are. The only ones that aren't are
phosphoniums. I could use it as PTC but that would be a waste since TBAB is a lot cheaper.
|
|
Chris The Great
Hazard to Others
Posts: 463
Registered: 29-10-2004
Location: Canada
Member Is Offline
Mood: No Mood
|
|
I believe trimethylaluminum is considered an ionic liquid as it conducts electricity. Mp = 15 *C.
|
|
docberto
Harmless
Posts: 20
Registered: 29-5-2005
Member Is Offline
Mood: No Mood
|
|
It doesn't seem likely that trimethylaluminum would be considered an ionic liquid. It is an organometallic compound, and I doubt the bonds have
that much ionic character. I also am skeptical that it would conduct electricity. How readily would the carbanion and the aluminum cation
dissociate? Electricity needs free charges. Do you have any refs?
|
|
Chris The Great
Hazard to Others
Posts: 463
Registered: 29-10-2004
Location: Canada
Member Is Offline
Mood: No Mood
|
|
Well, I'm gonna have to admit I don't have a source for that because I had searched for hours before I found that looking for reaction
information on methyllithium, and now I have no clue where it was from. I don't think it conducts electricity very well though, it just
mentioned that it can.
However, if methyl sodium or methyl potassium are liquids they will be ionic.
http://www.mhhe.com/physsci/chemistry/carey/student/olc/ch14...
Unfortunately I can't find information on them, such as physical properties. Certainly an interesting group of (off-topic) compounds though.
But, organometals will not work as ionic solvents even though alot of them are liquids, as they tend to react with everything.
|
|
Lambda
National Hazard
Posts: 566
Registered: 15-4-2005
Location: Netherlands
Member Is Offline
Mood: Euforic Online
|
|
Available for download: Ionic liquids in synthesis (P. Wasserscheid & T. Welton)
Available for download:
A nice book on "Ionic liquids in synthesis" written by P. Wasserscheid and T. Welton. This book is a good image scan in DJVU format (4.13
mb) and has 380 pages reprinted in 2002.
Ionic liquids in synthesis (P. Wasserscheid & T. Welton 2002) (4.13 mb):
http://rapidshare.de/files/2810386/Ionic_liquids_in_synthesi...
|
|