So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Rajput, Jaisheila; Moss, John R.; Hutton, Alan T.; Hendricks, Denver T.; Arendse, Catherine E.; Imrie, Christopher researched the compound: Bromoferrocene( cas:1273-73-0 ).Electric Literature of C10BrFe.They published the article 《Synthesis, characterization and cytotoxicity of some palladium(II), platinum(II), rhodium(I) and iridium(I) complexes of ferrocenylpyridine and related ligands. Crystal and molecular structure of trans-dichlorobis(3-ferrocenylpyridine)palladium(II)》 about this compound( cas:1273-73-0 ) in Journal of Organometallic Chemistry. Keywords: ferrocenyl pyridine preparation redox potential reaction Group VIII complex; palladium ferrocenylpyridine complex preparation structure cyclic voltammetry human cytotoxicity; platinum pyridinylferrocene chloro complex preparation human cytotoxicity; iridium rhodium pyridylferrocene complex human cytotoxicity structure activity relationship; crystal structure palladium ferrocenylpyridine chloro complex; mol structure palladium ferrocenylpyridine chloro complex. We’ll tell you more about this compound (cas:1273-73-0).
The preparation of a series of ferrocenyl nitrogen donor ligands including ferrocenylpyridines, ferrocenylphenylpyridines and 1,1′-di(2-pyridyl)ferrocene is described. Coordination studies of the substituted pyridines (L) were carried out with platinum, palladium, rhodium and iridium. This resulted in the preparation of the following types of complexes: [MCl(CO)2(L)] and [M(cod)(L)2]ClO4 where M = Rh or Ir, cod = 1,5-cyclooctadiene; [M’Cl2(L)2] where M’ = Pt or Pd. The X-ray crystal structure of trans-dichlorobis(3-ferrocenylpyridine)palladium was obtained. The complexes were screened for activity against two human cancer cell lines. At least two of the complexes displayed growth inhibition similar to that of the widely used chemotherapeutic agent, cisplatin.
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Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com