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Updated: Feb 3, 2026

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
Published on: December 29, 2016
The coordination behaviour and reactivity of partially silicon based crown ethers towards beryllium chloride
Magnus R Buchner1, Matthias Müller, Fabian Dankert
1Anorganische Chemie, Nachwuchsgruppe Berylliumchemie, Fachbereich Chemie, Philipps-Universität Marburg, Hans-Meerwein-Straße 4, 35032 Marburg, Germany. magnus.buchner@chemie.uni-marburg.de.
Abstract:
Through reactions of 1,2-disila[12]crown-4 or 1,2-disila-benzo[12]crown-4 ethers with BeCl2 eight-membered Be-O-heterocycles, which are annulated by two six-membered Be-O-cycles were obtained and characterised. The reactions leading to these unusual ring systems have been investigated by NMR and IR spectroscopy as well as reactions with further ligand derivatives.
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Ethers can be prepared from organic compounds by various methods. Some of them are discussed below,
Preparation of Ethers by Alcohol Dehydration
In this method, in the presence of protic acids, alcohol dehydrates to produce alkenes and ethers under different conditions. For example, in the presence of sulphuric acid, dehydration of ethanol at 413 K yields ethoxyethane, whereas it yields ethene at 443 K.
Structure and Nomenclature of Ethers
Ethers are organic compounds with an ether functional group which is characterized by an oxygen atom connected to two — identical or different — alkyl, aryl, or vinyl groups. The C–O–C linkage in dimethyl ether — the simplest ether — has an approximately tetrahedral bond angle of 110.3 degrees. The oxygen atom is sp3- hybridized, with the C–O distance being about 140 pm.
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