A Homologous Series of Regioselectively Tetradeprotonated Group 8 Metallocenes: New Inverse Crown Ring Compounds Synthesized via a Mixed Sodium−Magnesium Tris(diisopropylamide) Synergic Base

Subjecting ferrocene, ruthenocene, or osmocene to the synergic amide base sodium−magnesium
tris(diisopropylamido) affords a unique homologous series of metallocene derivatives of general formula
[{M(C5H3)2}Na4Mg4(i-Pr2N)8] (where M = Fe (1), Ru (2), or Os (3)). X-ray crystallographic studies of 1−3
reveal a common molecular “inverse crown” structure comprising a 16-membered [(NaNMgN)4]4+ “host”
ring and a metallocenetetraide [M(C5H3)2]4- “guest” core, the cleaved protons of which are lost selectively
from the 1, 1‘, 3, and 3‘-positions. Variable-temperature NMR spectroscopic studies indicate that 1, 2, and
3 each exist as two distinct interconverting conformers in arene solution, the rates of exchange of which
have been calculated using coalescence and EXSY NMR measurements.