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Dioxolane

Manufactured by Merck Group
Sourced in Germany, United States

Dioxolane is a cyclic acetal compound used as a chemical reagent and solvent in various laboratory applications. It functions as a protective group for carbonyl compounds and is often utilized in organic synthesis reactions. The core function of dioxolane is to provide a temporary protecting group for carbonyl groups, enabling selective transformations in complex organic molecules.

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4 protocols using dioxolane

1

Synthesis of Lithium-Sulfur Battery Materials

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Sublimed sulfur (≥99.5%), bis(trifluoromethane)sulfonimide lithium salt (LiTFSI), anhydrous lithium nitrate, dioxolane (DOL, 99%) 1,2-dimethoxyethane (anhydrous DME, 99.5%), and analytical grade chemicals such as KMnO4 were procured from Sigma Aldrich. Polyvinylidene fluoride (PVDF), N-methyl pyrrolidinone (NMP) and Super P were purchased from Alfa Aesar. l-glycine was procured from Fischer Scientific. All chemicals were used as received without further purification.
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2

Solubility and Electrochemical Analysis of Li-BL

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Solubility tests were conducted by dissolving a few milligrams of Li-BL in N-methyl-2-pyrrolidone (Sigma Aldrich), de-ionized water, a mixture of ethylene carbonate (Sigma Aldrich): dimethyl carbonate (Sigma Aldrich) 1 : 1 v/v, dioxolane (Sigma Aldrich), dimethoxymethane (Sigma Aldrich) and tetraethylene glycol dimethyl ether (Sigma Aldrich). Electrochemical measurements were conducted using CR2032-type coin cells (MTI) with quartz membrane (Whatman) as a separator. The electrolyte was prepared by mixing bis(trifluoromethylsulfonyl) amine lithium salt (Sigma Aldrich) in tetraethylene glycol dimethyl ether (TEGDME). Fabrication of coin cells was conducted in an argon-filled glove box. Cyclic voltammetry and electrochemical impedance spectroscopy were measured with an Autolab PGSTAT 302 N potentiostat. Galvanostatic charge–discharge tests were performed on LAND CT2001A battery tester and on an Arbin Instruments BT-2000 battery cycler.
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3

Synthesis and Characterization of Polyoxyethylene Diols

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Chemicals: chloroform-d1, 99.6% (Deutero GmbH, Kastellaun, Germany); dichlorobenzene, anhydrous, 99% (Sigma-Aldrich Chemie GmbH, Taufkirchen, Germany), secure seal, withdrawn under counter current argon flow; dichloromethane, anhydrous, ≥99.8% (Sigma-Aldrich), secure seal, withdrawn under counter current argon flow; dioxolane, anhydrous, 99.8% (Sigma-Aldrich), secure seal, withdrawn under counter current argon flow; n-pentane, technical, >98% (Haltermann Carless, Hamburg, Germany); sulfur trioxide DMF complex, 97+ % (ACROS Organics, Geel, Belgium); triethylamine, >98% (Fluka Analytical, Merck KGaA, Darmstadt, Germany); trioxane, ≥99% (Sigma-Aldrich). These were used as supplied if not stated otherwise. Polyoxyethylene diols A, B, and C were obtained with nominal weights of 1000, 400 and 200 g/mol, respectively, as PEG 1000, (Fluka, Honeywell Specialty Chemicals Seelze GmbH, Seelze, Germany), PEG 400, (Fluka), and PEG 200 for synthesis (Merck KGaA, Darmstadt, Germany); they were then dried in an oil pump vacuum prior to used. The number average molecular weights were determined with gel permeation chromatography, being 1076, 364 and 136 g/mol, respectively.
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4

Electrochemical Characterization of Dioxolane Electrolytes

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Dioxolane (DOL), 1,2-dimethoxyethane (DME), benzoquinone, acetonitrile (AN), pyrrole, 1-butyl-3-methyl imidazolium chloride (BMImCl), Li and Al foils were purchased from Sigma, USA. Aluminium chloride (AlCl 3 ) and zinc foil were obtained from Alfa Aesar, USA. Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) and zinc bis(trifluoromethanesulfonyl)imide (ZnTFSI) were purchased from Solvionic, France.
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