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The preparation and properties of sulphur nitride and thiotrithiazyl chloride

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dc.contributor.author MacDiarmid, Alan
dc.date.accessioned 2010-11-22T23:18:15Z
dc.date.accessioned 2022-10-24T23:54:12Z
dc.date.available 2010-11-22T23:18:15Z
dc.date.available 2022-10-24T23:54:12Z
dc.date.copyright 1949
dc.date.issued 1949
dc.identifier.uri https://ir.wgtn.ac.nz/handle/123456789/22603
dc.description.abstract 1. It is shown that acetyl chloride reacts with sulphur nitride to give diacetamide, sulphur dioxide, and possibly sulphur chlorides, as well as thiotrithiazyl chloride. 2. Hydrogen chloride alone, reacts with sulphur nitride to form thiotrithiazyl chloride. Its preparation from acetyl chloride and sulphur chloride, is presumably due to the small amount of free hydrogen chloride always present in these reagents. 3. Hydrogen bromide and hydrogen iodide react with sulphur nitride also, apparently forming thiotrithiazyl bromide, and thiotrithiazyl iodide respectively. 4. Thiotrithiazyl chloride is easily decomposed by methyl alcohol and ethyl acetate to reform sulphur nitride. 5. Several proposed structures for sulphur nitride are discussed. A tetrahedral structure for sulphur nitride is suggested, which agrees with its chemical properties and also with modern X-ray data. en_NZ
dc.format pdf en_NZ
dc.language en_NZ
dc.language.iso en_NZ
dc.publisher Te Herenga Waka—Victoria University of Wellington en_NZ
dc.title The preparation and properties of sulphur nitride and thiotrithiazyl chloride en_NZ
dc.type Text en_NZ
vuwschema.type.vuw Awarded Research Masters Thesis en_NZ
thesis.degree.grantor Te Herenga Waka—Victoria University of Wellington en_NZ
thesis.degree.level Masters en_NZ
thesis.degree.name Master of Science en_NZ


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