Derivation of elementary reaction about 1273-73-0

From this literature《Synthesis, structure and reactivity study of 1,1′-bis(N-tert-butyl-N-hydroxyamino)ferrocene》,we know some information about this compound(1273-73-0)HPLC of Formula: 1273-73-0, but this is not all information, there are many literatures related to this compound(1273-73-0).

Carre, Francis; Guerin, Christian; Henner, Bernard J. L.; Uerpmann, Carsten published an article about the compound: Bromoferrocene( cas:1273-73-0,SMILESS:Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25 ).HPLC of Formula: 1273-73-0. Aromatic heterocyclic compounds can be classified according to the number of heteroatoms or the size of the ring. The authors also want to convey more information about this compound (cas:1273-73-0) through the article.

The synthesis of 1,1′-bis(N-tert-butyl-N-hydroxyamino)ferrocene (1) is described, and the x-ray anal. showed eclipsed positions of the two tert-butylhydroxyamino groups. This structure can be explained by the interactions of the hydroxyl hydrogens with the N atoms of the other tert-butylhydroxyamino group. This interaction is maintained in solution and may explain that the oxidation of 1 using Ag2O gave a decomposition reaction instead of the expected 1,1′-bis(N-tert-butylaminoxy)ferrocene. The ESR spectrum of an oxidized solution of 1 showed a 1:1:1 triplet, but it corresponded only to traces of an N-O• radical. Cyclic voltammograms of 1 showed that it is more easily oxidized than ferrocene and less easily than 1,1′-diaminoferrocene, indicating that chem. oxidation of 1 occurs in the ferrocenyl part of the mol., followed by rapid decomposition

From this literature《Synthesis, structure and reactivity study of 1,1′-bis(N-tert-butyl-N-hydroxyamino)ferrocene》,we know some information about this compound(1273-73-0)HPLC of Formula: 1273-73-0, but this is not all information, there are many literatures related to this compound(1273-73-0).

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com