Abstract

AbstractThe following chiral organometallic complexes of the cinchona alkaloids quinine (L1), cinchonidine (L2), quinidine (L3), cinchonine (L4) were prepared: [(η5‐C5H5)(Ph3P)(OC)‐Ru(L)]BF4 (1: L=L1; 2: L=L2; 3: L=L3), ClAuL1 (4), [(η5‐C5Me5)(Cl2)Ir(L)] (5: L=L1; 6: L=L2; 7: L=L4), [(η5‐C5Me5)(Cl2)Rh(L2)] (8), [(η6‐p‐cymene)(Cl2)Ru(L)] (9: L=L1; 10: L=L2; 11: L=L4). In all complexes the tertiary nitrogen atom of the cinchona alkaloids is bound to the metal. Complexes 5 – 11 are formed as mixtures of isomers. Elimination of HCl from 10 and 11 gives the neutral N,O‐chelate complexes (η6‐p‐cymene)(Cl)Ru(L2 – H+) (13) and (η6‐p‐cymene)‐(Cl)Ru(L4 – H+) (14) which were structurally characterized by X‐ray diffraction.

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