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Cationic Iridium Complexes with Chiral Dithioether Ligands: Synthesis, Characterisation and Reactivity under Hydrogenation Conditions
Author(s) -
FloresSantos Leticia,
Martin Erika,
Aghmiz Ali,
Diéguez Montserrat,
Claver Carmen,
MasdeuBultó Anna M.,
MuñozHernández Miguel Ángel
Publication year - 2005
Publication title -
european journal of inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.667
H-Index - 136
eISSN - 1099-0682
pISSN - 1434-1948
DOI - 10.1002/ejic.200400828
Subject(s) - chemistry , diastereomer , cationic polymerization , metallacycle , stereochemistry , ligand (biochemistry) , bicyclic molecule , reactivity (psychology) , iridium , sulfur , enantioselective synthesis , medicinal chemistry , catalysis , organic chemistry , x ray crystallography , medicine , biochemistry , receptor , alternative medicine , pathology , physics , diffraction , optics
A series of cationic Ir I complexes containing chiral dithioether ligands have been prepared in order to study the influence of the sulfur substituents and the metallacycle size on the acetamidoacrylate hydrogenation reaction. In the case of complexes 6 , 7 and 10 , a mixture of diastereomers is observed in solution due to the sulfur inversion processes. In contrast, this fluxional behaviour is efficiently controlled by using bicyclic ligands which inhibit the S‐inversion in complexes 8 and 9 . The solid‐state structure of complex 10b shows only one diastereomer with the sulfur substituents in a relative anti disposition and in an overall configuration of S C S C S S S S at the coordinated dithioether ligand. Iridium complexes containing seven‐ and six‐membered metallacycles ( 6b – d , 7b ,c, 10a , b ) react with the substrate through S‐ligand substitution, and the rate of this substitution is related to the position of the fluorine atom on the aromatic ring. On the contrary, complexes containing a bis metallacycle ( 8 and 9 ) are not displaced by the substrate. The catalytic hydrogenation activity of complexes 8 and 9 is analysed in terms of the high stability of the corresponding dihydride complexes ( 13 and 14 ). In both cases, only two of the four possible diastereomeric dihydride species are formed in solution. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005)