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Aromaticity of the Cyclobutadiene Dianion:  Structural Characteristics and Magnetic Properties

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Department of Chemistry, University of Tsukuba, Tsukuba, Ibaraki 305-8571, Japan
Cite this: Organometallics 2002, 21, 6, 1072–1076
Publication Date (Web):February 19, 2002
https://doi.org/10.1021/om010902o
Copyright © 2002 American Chemical Society
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Abstract

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The dilithium salts of cyclobutadiene dianions (CBD2-), 1,2-diphenyl-3,4-bis(trimethylsilyl)cyclobutadiene dianion dilithium (3), and 1,3-diphenyl-2,4-bis(trimethylsilyl)cyclobutadiene dianion dilithium (4) have been synthesized by the reaction of the corresponding cyclobutadiene cobalt complexes with lithium metal in tetrahydrofuran (THF). The dilithium salts were isolated as air- and moisture-sensitive crystals, and their molecular structures, containing two molecules of 1,2-dimethoxyethane (DME), were determined by X-ray crystallography. Each of the CBD2- has a monomeric structure and forms contact ion pairs (CIPs) in the crystal. The two Li+ ions are located above and below the plane of the four-membered ring and are bonded to the four quaternary carbon atoms. The cyclobutadienediide ring of the cis-diphenyl CBD2- (3) shows a conspicuous trapezoid structure, whereas that of the trans-diphenyl CBD2- (4) shows a slightly rhomboid structure. The 7Li NMR spectra of the CBD2- indicate that the two lithium atoms are considerably shielded by a diatropic ring current, resulting from the six-π-electron system.

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 Present address:  Institute for Molecular Science, Myodaiji, Okazaki 444-8585, Japan.

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Tables giving the details of the X-ray structure determination, thermal ellipsoid plots, fractional atomic coordinates, anisotropic thermal parameters, bond lengths, and bond angles for 3 and 4. This material is available free of charge via the Internet at http://pubs.acs.org.

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  20. Kazunori Takanashi, Akira Inatomi, Vladimir Ya. Lee, Masaaki Nakamoto, Masaaki Ichinohe, Akira Sekiguchi. Tetrakis(trimethylsilyl)cyclobutadiene Dianion Alkaline Earth Metal Salts: New Members of the 6π-Electron Aromatics Family. European Journal of Inorganic Chemistry 2008, 2008 (11) , 1752-1755. https://doi.org/10.1002/ejic.200800066
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  27. Jose M. Mercero, Jon M. Matxain, Jesus M. Ugalde. Mono- and Multidecker Sandwich-Like Complexes of the Tetraazacyclobutadiene Aromatic Ring. Angewandte Chemie International Edition 2004, 43 (41) , 5485-5488. https://doi.org/10.1002/anie.200460498
  28. M. Sebastian, O. Schmidt, A. Fuchs, M. Nieger, D. Szieberth, L. Nyulaszi, E. Niecke. FROM 1,3-DIPHOSPHETANE-2,4-DIYLS TO CYCLIC ANIONS AND CATIONS. Phosphorus, Sulfur, and Silicon and the Related Elements 2004, 179 (4-5) , 779-783. https://doi.org/10.1080/10426500490427024
  29. Tsukasa Matsuo, Akira Sekiguchi. Cyclobutadiene Dianion. Bulletin of the Chemical Society of Japan 2004, 77 (2) , 211-226. https://doi.org/10.1246/bcsj.77.211

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