An update on the compound challenge: 1273-73-0

Although many compounds look similar to this compound(1273-73-0)Application of 1273-73-0, numerous studies have shown that this compound(SMILES:Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Application of 1273-73-0. The mechanism of aromatic electrophilic substitution of aromatic heterocycles is consistent with that of benzene. Compound: Bromoferrocene, is researched, Molecular C10BrFe, CAS is 1273-73-0, about Triferrocenyl complexes of tungsten(VI): the molecular structure in the solid state and dynamic behavior in solution of triferrocenyl(ferrocenyloxy)oxotungsten, WO(OFc)Fc3. Author is Herberhold, Max; Kniesel, Heidemarie; Haumaier, Ludwig; Thewalt, Ulf.

WO(X)Fc3 [X = Cl (I), OMe (II), OFc (III), OBu (IV); Fc = ferrocenyl] were obtained by treating WOCl4 with ferrocenyllithium in THF. Reaction of WOCl4 with a threefold excess of FcLi gives I, which may be converted into II using KOMe. Reaction of WOCl4 with a sixfold excess of FcLi gives a mixture containing III and IV in addition to ferrocene and biferrocene. According to the x-ray crystallog. anal., III has a trigonal-bipyramidal structure with three ferrocenyl ligands occupying the equatorial positions and an axial ferrocenoxy group coordinated trans to the oxo ligand. The three W-C(ferrocenyl) (average 2.092 Å) and the O-C(ferrocenyl) [1.33(1) Å] bond distances are remarkably short. The axial tungsten-oxygen distances correspond to a W:O double and a W-O single bond, resp. The 1H and 13C NMR spectra of III are temperature dependent because of a hindered rotation of the ferrocenyl ligands around the W-C(ferrocenyl) bonds.

Although many compounds look similar to this compound(1273-73-0)Application of 1273-73-0, numerous studies have shown that this compound(SMILES:Br[C-]12[Fe+2]3456789([C-]%10C6=C7C8=C9%10)C1=C3C4=C25), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
Thiazolidine – Wikipedia,
Thiazolidine – ScienceDirect.com