Journal of Organometallic Chemistry p. 303 - 312 (1994)
Update date:2022-08-05
Topics:
Uno, Mitsunari
Ando, Katsuhiro
Komatsuzaki, Nobuko
Tsuda, Takehiro
Tanaka, Takanori
et al.
The first diastereomerically pureplanar-chiral cyclopentadienyl-cobalt complexes (4 and 5) have been synthesised by the reaction of CoCl(PPh3)3 with a trisubstituted cyclopentadienyl anion having a (-)-menthyl group in the presence of diarylacetylenes.Removal of the menthyl group from 4a and 5a afforded the first optically pure enantiomers of planar-chiral cyclopentadienylcobalt complexes, (+)- and (-)-6, and (+)- and (-)-7.The molecular structure including absolute configuration of 4a has been established by a single-crystal X-ray structure analysis.Crystallographic data for 4a: orthorhombic, space group P212121; a = 18.602(10), b = 15.629(3), c = 13.893(3) Angstroem; Z = 4; R = 0.051, Rw = 0.057.The structure of 4a indicates that there exist three different chiralities
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