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An orthorhombic polymorph of 2-(1,3,5-dithiazinan-5-yl)ethanol or MEA-dithiazine
Substituted triazines are a class of compounds utilized for scavenging and sequestering hydrogen sulfide in oil and gas production operations. The reaction of one of these triazines under field conditions resulted in the formation of the title compound, 2-(1,3,5-dithiazinan-5-yl)ethanol, C(5)H(11)...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8819450/ https://www.ncbi.nlm.nih.gov/pubmed/35145749 http://dx.doi.org/10.1107/S2056989022000342 |
Sumario: | Substituted triazines are a class of compounds utilized for scavenging and sequestering hydrogen sulfide in oil and gas production operations. The reaction of one of these triazines under field conditions resulted in the formation of the title compound, 2-(1,3,5-dithiazinan-5-yl)ethanol, C(5)H(11)NOS(2), or MEA-dithiazine. Polymorphic form I, in space group I4(1)/a, was first reported in 2004 and its extended structure displays one-dimensional, helical strands connected through O—H⋯O hydrogen bonds. We describe here the form II polymorph of the title compound, which crystallizes in the orthorhombic space group Pbca as centrosymmetric dimers through pairwise O—H⋯N hydrogen bonds from the hydroxyl moiety to the nitrogen atom of an adjacent molecule. |
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