Sciencemadness Discussion Board
Not logged in [Login ]
Go To Bottom

Printable Version  
Author: Subject: Iron pentacarbonyl synthesis...
evil_lurker
National Hazard
****




Posts: 767
Registered: 12-3-2005
Location: United States of Elbonia
Member Is Offline

Mood: On the wagon again.

[*] posted on 21-3-2007 at 10:02
Iron pentacarbonyl synthesis...


I can't seem to find any sort of information on how this compound is produced... I've googled the hell out of it and dug thru a crapload of patents, but none deal with the actual synthesis.

I'm thinking that maybe using a flask with some activated iron powder, evacuate with a vacuum pump, then pressurize with carbon monoxide @60-100ºC and leave sitting in the dark for a couple days and see what happens.
View user's profile View All Posts By User
matei
Hazard to Others
***




Posts: 205
Registered: 16-9-2006
Member Is Offline

Mood: No Mood

[*] posted on 21-3-2007 at 10:06


Check Brauer - "Inorganic Synthesis".
View user's profile View All Posts By User
benzylchloride1
Hazard to Others
***




Posts: 299
Registered: 16-3-2007
Member Is Offline

Mood: Pushing the envelope of synthetic chemistry in one's basement

[*] posted on 11-1-2009 at 21:05


I am currently researching methods of producing this compound at atmospheric pressure. I found a procedure that looks to be fairly simple for producing this compound in small amounts from fairly easy to obtain chemicals. Here is the procedure from Synthesis of Organometallic Compounds:

Iron powder (5.0 g) is suspended in dry heptane (30 mL) and is activated by shaking
for 15 min in an atmosphere of H 2 S, A slight gas evolution on the surface of the iron
particles is observed during the activation. The suspension is then stored under nitro-
gen. After introduction of DCO or C I8 0 at atmospheric pressure, the suspension is
stirred at room temperature very vigorously for 20 h. The solution gradually turns red
during the reaction. The solvent is then removed under reduced pressure. The title
product is obtained by distillation at atmospheric pressure (bp 103 0q.
Properties: mp -20°C. bp 103°C. IR [Fe(CO)s in C 6 H I2 ]: 2022, 2000 cm- I .
[Fe(COkl 3 CO)n]: 2023, 200 I, 1988, 1976, 1972, 1964, 1955 cm- l ; [Fe(COkn(C I8 0)n]:
2023,2008,200 I, 1988, 1976, 1964, 1955 cm I.
Pentacarbonyliron is a straw-colored liquid with a musty odor, which is stable in air
at room temperature. It should be handled in a hood because it is a toxic liquid with a
relatively high vapor pressure even at room temperature (21 mmHg, 20°C). It should
be stored in the dark to prevent slow decomposition.

The iron powder can be obtained from hand warmers. Certain disposable hand warms have finely divided iron in them that rapidly reacts with oxygen for produce heat and iron oxide. The hand warmer would have to be opened up under the heptane due to the air sensitive nature of the finely divided iron. The carbon monoxide could be produced by reacting oxalic or formic acid with concnetrated sulfuric acid. Be sure to conduct this step in a powerful exhaust hood or out side on a breezy day due to the highly poisonous nature of the carbon monoxide and the pentacarbonyl iron product. I have not conducted this procedure, but I plan on running it in the near future.

[Edited on 11-1-2009 by benzylchloride1]
View user's profile View All Posts By User

  Go To Top