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

• Published in: Journal of the American Chemical Society 2004-09, Vol.126 (37), p.11612-11620
• Main Authors: Andrikopoulos, Prokopis C, Armstrong, David R, Clegg, William, Gilfillan, Carly J, Hevia, Eva, Kennedy, Alan R, Mulvey, Robert E, O'Hara, Charles T, Parkinson, John A, Tooke, Duncan M
• Format: Article
• Language: English
• Subjects: Chemistry; Condensed matter: structure, mechanical and thermal properties; Coordination compounds; Exact sciences and technology; Inorganic chemistry and origins of life; Inorganic compounds; Metal complexes; Physics; Preparations and properties; Structure of solids and liquids; crystallography; Structure of specific crystalline solids
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/ja0472230

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.