Jump to content

Stability of organo-metallic compounds


pulkit
 Share

Recommended Posts

Not too long ago I had the oppurtunity to work with ferrocene in the lab. I proceeded to carry out an acetylation reaction on the compound. What did astound me was the stability of ferrocene, a pale orange powder at room temperature.......can anyone explain why it is so stable ? The reason why I ask is that looking at its molecular structure it seemed to me to be unstable in nature. And if it is indeed so stable how come no one could synthesize it before the mid 20th century.

 

One organo-metallic I have extensicesly studied is the Grignard reagent, unfortunately I never acctualy had a chance to deal with the chemical, can anyone please comment on its stability and physical state at room temperature ?

Link to comment
Share on other sites

The process for preparing stable high oxidation state ferrocene derivatives, namely Fe(III)/Fe(IV), by reacting ferrocene derivatives in which one or more electron-donating groups are covalently bonded to the cyclopentadienyl rings with electron-donating ligands having strong coordinative groups for ferric species.

 

(APP 2001)

Link to comment
Share on other sites

Create an account or sign in to comment

You need to be a member in order to leave a comment

Create an account

Sign up for a new account in our community. It's easy!

Register a new account

Sign in

Already have an account? Sign in here.

Sign In Now
 Share

×
×
  • Create New...

Important Information

We have placed cookies on your device to help make this website better. You can adjust your cookie settings, otherwise we'll assume you're okay to continue.