Selenothiophosphinic Acid Salts
An efficient synthesis of selenothiophosphinic acid salts is achieved by reacting selenothiophosphinic acid S-(2-trimethylsilyl)ethyl esters with ammonium or alkali metal fluorides. The X-ray structure analysis of the potassium 18-crown-6 selenothiophosphinic acid salt shows that the salt is monomer...
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Veröffentlicht in: | Chemistry letters 2002-09, Vol.31 (9), p.914 |
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creator | Murai, Toshiaki Kimura, Tsutomu Miwa, Akihiro Kurachi, Daisuke Kato, Shinzi |
description | An efficient synthesis of selenothiophosphinic acid salts is achieved by reacting selenothiophosphinic acid S-(2-trimethylsilyl)ethyl esters with ammonium or alkali metal fluorides. The X-ray structure analysis of the potassium 18-crown-6 selenothiophosphinic acid salt shows that the salt is monomeric. Alkylation of the salts proceeds at the selenium atom whereas acylation occurs at the sulfur atom. |
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The X-ray structure analysis of the potassium 18-crown-6 selenothiophosphinic acid salt shows that the salt is monomeric. 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The X-ray structure analysis of the potassium 18-crown-6 selenothiophosphinic acid salt shows that the salt is monomeric. 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The X-ray structure analysis of the potassium 18-crown-6 selenothiophosphinic acid salt shows that the salt is monomeric. Alkylation of the salts proceeds at the selenium atom whereas acylation occurs at the sulfur atom.</abstract><cop>Tokyo</cop><pub>Chemical Society of Japan</pub></addata></record> |
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source | Oxford University Press Journals All Titles (1996-Current) |
title | Selenothiophosphinic Acid Salts |
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