Abstract: | The chiral‐at‐metal cycloheptatrienyl‐molybdenum complexes (RMo, SC)‐(η7‐C7H7)Mo(iminphos)(CO)]BF4 ( 2a ) and (SMo, SC)‐(η7‐C7H7)Mo(iminphos)(CO)]BF4 ( 2b ) (iminphos = 2‐N‐(S)‐1‐phenylethylcarbaldimino]phenyl(diphenyl)phosphane), which only differ in the molybdenum configuration, were prepared and separated by fractional crystallization. The absolute configuration for both diastereomers was determined by X‐ray analysis. 1H NMR studies demonstrated the configurational lability at the molybdenum centre in solution. |