2001Angewandte Chemie International EditionRequires access

From a Cyclobutadiene Dianion to a Cyclobutadiene: Synthesis and Structural Characterization of Tetrasilyl-Substituted Cyclobutadiene

Akira Sekiguchi, Masanobu Tanaka, Tsukasa Matsuo, Hidetoshi Watanabe

Open publisher page 68 citations

Abstract

In less than one minute dianion 1 can be oxidized with 1,2-dibromoethane to give pure tetrakis(trimethylsilyl)cyclobutadiene (2, see scheme). The bridged cyclobutadiene derivative 6 was also similarly synthesized and characterized by X-ray crystallography; it exhibits a planar rectangular structure with localized C=C bonds.

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What this paper is about

In less than one minute dianion 1 can be oxidized with 1,2-dibromoethane to give pure tetrakis(trimethylsilyl)cyclobutadiene (2, see scheme). The bridged cyclobutadiene derivative 6 was also similarly synthesized and characterized by X-ray crystallography; it exhibits a planar rectangular structure with localized C=C bonds.

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OpenAlex reports 68 citations for this work. Citation counts describe recorded attention and do not establish research quality.

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Available abstract

In less than one minute dianion 1 can be oxidized with 1,2-dibromoethane to give pure tetrakis(trimethylsilyl)cyclobutadiene (2, see scheme). The bridged cyclobutadiene derivative 6 was also similarly synthesized and characterized by X-ray crystallography; it exhibits a planar rectangular structure with localized C=C bonds.

Key concepts: Cyclobutadiene, Characterization (materials science), Chemistry, Materials science, Organic chemistry, Nanotechnology, Molecule

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From a Cyclobutadiene Dianion to a Cyclobutadiene: Synthesis and Structural Characterization of Tetrasilyl-Substituted Cyclobutadiene — Research Paper | ScholarLens