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Reversible deprotonation of [Fe(C5H5)(η6-fluorene)]PF6 and [Mn(η6-fluorene)(CO)3]PF6 initially produces zwitterionic complexes wherein co-ordination to the six-membered ring is retained, and the manganese complex very slowly reverts to the isomeric η5 complex, [Mn(η5-fluorenyl)(CO)3]; the X-ray structure of the iron compound [Fe(C5H5)(C13H9)] has been determined.
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Johnson et al. (1976) studied this question.
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