Polyhedral ferraboranes derived from the B5H8- ion. Analogs of

Chem. , 1979, 18 (12), pp 3291–3294. DOI: 10.1021/ic50202a001. Publication Date: December 1979. ACS Legacy Archive. Cite this:Inorg. Chem. 18, 12, 3...
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Volume 18

Inorganic Chemistry

Number 12

I

December 1979

0 Copyright 1979 by the American Chemical Society

Contribution from the Department of Chemistry, University of Virginia, Charlottesville, Virginia 22901

Polyhedral Ferraboranes Derived from the B5H8-Ion. Analogues of Ferrocene, Hexaborane( lo), and nido-B11H15 RICHARD WEISS and RUSSELL N. GRIMES* Received April 3, 1979

The reaction of B5Hs-, Fe2+,and C5H5-in THF at -78 'C followed by workup of the products in air gave violet 2-(q5yellow 2-(q2-C5H5)FeBloH15, and ferrocene, plus traces of other ferraboranes. From 'lB and 'H NMR C5H5)FeB5Hlo, spectra, 2-(q5-C5H5)FeB5Hlo was assigned a pentagonal-pyramidalstructure with iron in the base and five bridging hydrogen atoms (3 B-H-B and 2 Fe-H-B) on the open face. On being heated to 175-180 'C this compound rearranged to violet 1-(q5-C5H5)FeB5Hlo, in which the iron atom is proposed to occupy the apex position. Both isomers are electronic analogues of B6H10and ferrocene, and the 1-isomer is a direct structural analogue of ferrocene which contains a cyclic BSHlo-ligand, isoelectronicwith C5H