In organic chemistry, atoms other than carbon and hydrogen are generally referred to as heteroatoms. The most common heteroatoms are nitrogen, oxygen and sulfur. Now I present to you an article called The anomalous electrochemistry of the ferrocenylamines, published in 1986, which mentions a compound: 1273-73-0, mainly applied to ferrocenylamine electrochem oxidation; substituent effect electrochem ferrocenylamine; resonance ferrocenylamine, Recommanded Product: Bromoferrocene.
In the electrochem. of ferrocenylamines, the amine substituent acts as an unusually potent activating group for ferrocene oxidation, as shown by various Hammett-type correlations, with ferrocenylamine oxidizing at a potential 0.37 V more neg. than ferrocene itself. Triferrocenylamine, a compound with a nearly planar N, produces three reversible oxidation waves, the first of which is 0.31 neg. of ferrocene’s oxidation These and other data suggest that resonance interaction between ferrocene and the N lone pair is an important factor in ferrocene oxidation This contrasts with conclusions of earlier studies in which ferrocenes, with primarily electron-withdrawing groups, were examined
If you want to learn more about this compound(Bromoferrocene)Recommanded Product: Bromoferrocene, you may wish to communicate with the author of the article,or consult the relevant literature related to this compound(1273-73-0).
Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com