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Preparation of 4-benzylsulfanyl[1,2,3,5]dithiadiazol-1-ylium chlorides: potential precursors to meso-ionic 1,2,3,5-dithiadiazolium-4-thiolate

Preparation of 4-benzylsulfanyl[1,2,3,5]dithiadiazol-1-ylium chlorides: potential precursors to meso-ionic 1,2,3,5-dithiadiazolium-4-thiolate
Preparation of 4-benzylsulfanyl[1,2,3,5]dithiadiazol-1-ylium chlorides: potential precursors to meso-ionic 1,2,3,5-dithiadiazolium-4-thiolate
Treatment of S-benzyl-iso-thiuronium chlorides with sulfur monochloride (S2Cl2) gives the corresponding S-benzyl-1,2,3,5-thiadiazolium chlorides 2 as deep red crystalline compounds. The structure of the p-chlorobenzyl derivative 2a has been confirmed by X-ray crystallography. Attempts to generate the unknown type-B meso-ionic compound 1,2,3,5-dithiadiazolium-4-thiolate 1 by reaction of these salts with nucleophiles were unsuccessful. AM1 semi-empirical molecular orbital calculations suggest that, although the meso-ionic structure corresponds to a local energy minimum, acyclic valence tautomers could equilibrate in solution and lead to further reaction.
meso-ionic, 1, 2, 3, 5-dithiadiazolium salts, sulfur monochloride, s-benzyl-iso-thiuronium chlorides, am1 calculations, crystal-structure, salts, ring
1424-6376
224-233
Gelbrich, Thomas
42309d69-eaf1-4bb7-ba2e-db61f338e370
Humphries, Mark
7951676c-cd5b-4619-9eb6-91ebc054bb70
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Ramsden, Christopher A.
6369fadb-e248-41e8-b4f3-af7d6fbfbb6e
Gelbrich, Thomas
42309d69-eaf1-4bb7-ba2e-db61f338e370
Humphries, Mark
7951676c-cd5b-4619-9eb6-91ebc054bb70
Hursthouse, Michael B.
57a2ddf9-b1b3-4f38-bfe9-ef2f526388da
Ramsden, Christopher A.
6369fadb-e248-41e8-b4f3-af7d6fbfbb6e

Gelbrich, Thomas, Humphries, Mark, Hursthouse, Michael B. and Ramsden, Christopher A. (2002) Preparation of 4-benzylsulfanyl[1,2,3,5]dithiadiazol-1-ylium chlorides: potential precursors to meso-ionic 1,2,3,5-dithiadiazolium-4-thiolate. Arkivoc, vi, 224-233.

Record type: Article

Abstract

Treatment of S-benzyl-iso-thiuronium chlorides with sulfur monochloride (S2Cl2) gives the corresponding S-benzyl-1,2,3,5-thiadiazolium chlorides 2 as deep red crystalline compounds. The structure of the p-chlorobenzyl derivative 2a has been confirmed by X-ray crystallography. Attempts to generate the unknown type-B meso-ionic compound 1,2,3,5-dithiadiazolium-4-thiolate 1 by reaction of these salts with nucleophiles were unsuccessful. AM1 semi-empirical molecular orbital calculations suggest that, although the meso-ionic structure corresponds to a local energy minimum, acyclic valence tautomers could equilibrate in solution and lead to further reaction.

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More information

Published date: 2002
Additional Information: CF-530B
Keywords: meso-ionic, 1, 2, 3, 5-dithiadiazolium salts, sulfur monochloride, s-benzyl-iso-thiuronium chlorides, am1 calculations, crystal-structure, salts, ring

Identifiers

Local EPrints ID: 19744
URI: http://eprints.soton.ac.uk/id/eprint/19744
ISSN: 1424-6376
PURE UUID: e7c6ccca-e339-402c-8dd7-a1fe4072a21c

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Date deposited: 20 Feb 2006
Last modified: 11 Dec 2021 14:26

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Contributors

Author: Thomas Gelbrich
Author: Mark Humphries
Author: Christopher A. Ramsden

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