Bis(N-methyl-N-phenylcarbamoyl)disulfane
The title compound, C16H16N2O2S2, has been synthesized by several different high-yield routes, and has been encountered as a co-product in a number of reaction pathways, ever since it became of interest to our research program over 30 years ago. We now confirm the proposed molecular structure in whi...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
International Union of Crystallography
2012-05-01
|
Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536812016030 |
id |
doaj-2d658688662d4df7a7e3c679bbeb3e93 |
---|---|
record_format |
Article |
spelling |
doaj-2d658688662d4df7a7e3c679bbeb3e932020-11-24T22:08:23ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682012-05-01685o1550o155010.1107/S1600536812016030Bis(N-methyl-N-phenylcarbamoyl)disulfaneGeorge BaranyMaren PinkAlayne L. SchrollThe title compound, C16H16N2O2S2, has been synthesized by several different high-yield routes, and has been encountered as a co-product in a number of reaction pathways, ever since it became of interest to our research program over 30 years ago. We now confirm the proposed molecular structure in which the molecule exhibits a twofold axis of symmetry through the mid-point of the S—S bond and the two planes defined by the (carbamoyl)sulfenyl moieties are essentially perpendicular to each other [dihedral angle = 81.55 (14)°].http://scripts.iucr.org/cgi-bin/paper?S1600536812016030 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
George Barany Maren Pink Alayne L. Schroll |
spellingShingle |
George Barany Maren Pink Alayne L. Schroll Bis(N-methyl-N-phenylcarbamoyl)disulfane Acta Crystallographica Section E |
author_facet |
George Barany Maren Pink Alayne L. Schroll |
author_sort |
George Barany |
title |
Bis(N-methyl-N-phenylcarbamoyl)disulfane |
title_short |
Bis(N-methyl-N-phenylcarbamoyl)disulfane |
title_full |
Bis(N-methyl-N-phenylcarbamoyl)disulfane |
title_fullStr |
Bis(N-methyl-N-phenylcarbamoyl)disulfane |
title_full_unstemmed |
Bis(N-methyl-N-phenylcarbamoyl)disulfane |
title_sort |
bis(n-methyl-n-phenylcarbamoyl)disulfane |
publisher |
International Union of Crystallography |
series |
Acta Crystallographica Section E |
issn |
1600-5368 |
publishDate |
2012-05-01 |
description |
The title compound, C16H16N2O2S2, has been synthesized by several different high-yield routes, and has been encountered as a co-product in a number of reaction pathways, ever since it became of interest to our research program over 30 years ago. We now confirm the proposed molecular structure in which the molecule exhibits a twofold axis of symmetry through the mid-point of the S—S bond and the two planes defined by the (carbamoyl)sulfenyl moieties are essentially perpendicular to each other [dihedral angle = 81.55 (14)°]. |
url |
http://scripts.iucr.org/cgi-bin/paper?S1600536812016030 |
work_keys_str_mv |
AT georgebarany bisnmethylnphenylcarbamoyldisulfane AT marenpink bisnmethylnphenylcarbamoyldisulfane AT alaynelschroll bisnmethylnphenylcarbamoyldisulfane |
_version_ |
1725816206422704128 |