1988
DOI: 10.1002/zaac.19885590118
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Beiträge zur Chemie der Schwefel‐Halogenide. 20. Di(methylthio)methyl‐ und Di(phenylthio)methylsulfonium‐hexafluoroarsenat und ‐hexachloroantimonat

Abstract: Es wird über die Darstellung und spektroskopische Charakterisierung der Di(methylthio)methyl‐ und Di(phenylthio)methylsulfonium‐Salze CH3S(SCH3)2+A− und CH3S(SC6H5)2+A− (A− = AsF6−, SbCl6−) berichtet. Ergänzend wird die Kristallstruktur von Di(methylthio)methylsulfoniumhexafluoroarsenat mitgeteilt.

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Cited by 14 publications
(2 citation statements)
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“…3,7 In Figure 6a we show the results of X-ray investigations on the dimers of [Se 2 Me 3 ]TeF 5 (17) 31 and [S 3 Me 3 ]AsF 6 (18a). 32 In Figure 6b a second modification of [S 3 Me 3 ]AsF 6 (18b) 33 is shown, in which four [S 3 Me 3 ] + units form a chain with short S•••S contacts (see Table 2). In the deep red colored salt [Se 3 Me 3 ]SbCl 6 (19) 34 the Se 3 Me 3 + units form a chain with short intermolecular Se•••Se distances.…”
Section: Noncovalent Chalcogen−chalcogen Interactions: Experimental R...mentioning
confidence: 99%
“…3,7 In Figure 6a we show the results of X-ray investigations on the dimers of [Se 2 Me 3 ]TeF 5 (17) 31 and [S 3 Me 3 ]AsF 6 (18a). 32 In Figure 6b a second modification of [S 3 Me 3 ]AsF 6 (18b) 33 is shown, in which four [S 3 Me 3 ] + units form a chain with short S•••S contacts (see Table 2). In the deep red colored salt [Se 3 Me 3 ]SbCl 6 (19) 34 the Se 3 Me 3 + units form a chain with short intermolecular Se•••Se distances.…”
Section: Noncovalent Chalcogen−chalcogen Interactions: Experimental R...mentioning
confidence: 99%
“…In the course of our studies of sulfur-rich compounds, synthetic pathways to trithiosulfonium salts were of general interest, since they contain the simplest structural fragment of a three-dimensional sulfur network. During our studies on reaction sequences for the formation of sulfur chains, connected to sulfonium cations, the condensation of S−H functional compounds with chlorosulfonium salts was found to be an excellent general pathway. The condensation of trichlorosulfonium salts with hydrogen sulfide (eq 1) yielded unstable trismercaptosulfonium salts, but attempts to obtain more stable organyl derivates by the use of mercaptanes failed (eq 1)…”
Section: Introductionmentioning
confidence: 99%