Volume 16, Issue 7 pp. 474-475
Communication
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Lithium 7bH-Indeno [1,2,3-jk] fluorenide, an Organolithium Compound Having a “Sandwich” Structure

Dipl.-Chem. Dieter Bladauski

Dipl.-Chem. Dieter Bladauski

Institut für Organische Chemie der Freien Universität Thielallee 63—67, D-1000 Berlin 33 (Germany)

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Prof. Dr. Hans Dietrich

Prof. Dr. Hans Dietrich

Dr. H. Dietrich Fritz-Haber-Institut der Max-Planck-Gesellschaft Faradayweg 4—6, D-1000 Berlin 33 (Germany)

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Dr. Hans-Jürgen Hecht

Dr. Hans-Jürgen Hecht

Institut für Organische Chemie der Freien Universität Thielallee 63—67, D-1000 Berlin 33 (Germany)

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Prof. Dr. Dieter Rewicki

Corresponding Author

Prof. Dr. Dieter Rewicki

Institut für Organische Chemie der Freien Universität Thielallee 63—67, D-1000 Berlin 33 (Germany)

Institut für Organische Chemie der Freien Universität Thielallee 63—67, D-1000 Berlin 33 (Germany)Search for more papers by this author
First published: July 1977
Citations: 21

Strained Alkyl-Aromatic Systems, Part 4. This work was supported by the Fonds der Chemischen Industrie.—Part 3: P. Luger, Ch. Tuchscherer, M. Grosse, D. Rewicki, Chem. Ber. 109, 2596 (1976).

Graphical Abstract

The organolithium compound (1) displays a variety of special features. Thus (1) is the first Li salt of a hydrocarbon having extreme charge delocalization in the carbanion, which crystallizes without heteroatom bases. Compound (1) is the first example of a substance in which Li is linearly coordinated with two hexahapto-bonded six-membered ring ligands. Moreover, there is no preferential orientation of the Li atoms on the C centers having the highest charge density.

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