Ammonium Oxathioamidate

Ammonium oxathioamidate (<b>1</b>) was synthesised by the reaction between <i>O</i>-ethyl-thioxamate (oxalic acid-1-amide-2-<i>O</i>-ethyl ester) and ammonium hydrogen carbonate in water solution. Compound <b>1</b> was fully characterised by both micro...

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Main Authors: M. Carla Aragoni, David B. Cordes, Anna Pintus, Enrico Podda, Riccardo Serra, Alexandra M. Z. Slawin, J. Derek Woollins, Massimiliano Arca
Format: Article
Language:English
Published: MDPI AG 2024-11-01
Series:Molbank
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Online Access:https://www.mdpi.com/1422-8599/2024/4/M1924
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author M. Carla Aragoni
David B. Cordes
Anna Pintus
Enrico Podda
Riccardo Serra
Alexandra M. Z. Slawin
J. Derek Woollins
Massimiliano Arca
author_facet M. Carla Aragoni
David B. Cordes
Anna Pintus
Enrico Podda
Riccardo Serra
Alexandra M. Z. Slawin
J. Derek Woollins
Massimiliano Arca
author_sort M. Carla Aragoni
collection DOAJ
description Ammonium oxathioamidate (<b>1</b>) was synthesised by the reaction between <i>O</i>-ethyl-thioxamate (oxalic acid-1-amide-2-<i>O</i>-ethyl ester) and ammonium hydrogen carbonate in water solution. Compound <b>1</b> was fully characterised by both microanalytical (elemental analysis, melting point determination) and spectroscopic means (FT-IR and NMR spectroscopy). Crystals suitable for single-crystal X-ray diffraction were isolated by slow evaporation of an ethanol solution of the compound. The analysis of the crystal packing reveals the prominent role exerted by intermolecular hydrogen bonding (HB) and chalcogen bonding (ChB) interactions.
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publishDate 2024-11-01
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series Molbank
spelling doaj-art-8b2028c14b3c4a3186e5ce2e2c7a6ba62024-12-27T14:42:16ZengMDPI AGMolbank1422-85992024-11-0120244M192410.3390/M1924Ammonium OxathioamidateM. Carla Aragoni0David B. Cordes1Anna Pintus2Enrico Podda3Riccardo Serra4Alexandra M. Z. Slawin5J. Derek Woollins6Massimiliano Arca7Dipartimento di Scienze Chimiche e Geologiche, Università Degli Studi Di Cagliari, S.S. 554 bivio Sestu, Monserrato, 09042 Cagliari, ItalyEaStCHEM School of Chemistry, University of St. Andrews, North Haugh, St. Andrews, Fife KY16 9ST, UKDipartimento di Scienze Chimiche e Geologiche, Università Degli Studi Di Cagliari, S.S. 554 bivio Sestu, Monserrato, 09042 Cagliari, ItalyDipartimento di Scienze Chimiche e Geologiche, Università Degli Studi Di Cagliari, S.S. 554 bivio Sestu, Monserrato, 09042 Cagliari, ItalyDipartimento di Scienze Chimiche e Geologiche, Università Degli Studi Di Cagliari, S.S. 554 bivio Sestu, Monserrato, 09042 Cagliari, ItalyEaStCHEM School of Chemistry, University of St. Andrews, North Haugh, St. Andrews, Fife KY16 9ST, UKEaStCHEM School of Chemistry, University of St. Andrews, North Haugh, St. Andrews, Fife KY16 9ST, UKDipartimento di Scienze Chimiche e Geologiche, Università Degli Studi Di Cagliari, S.S. 554 bivio Sestu, Monserrato, 09042 Cagliari, ItalyAmmonium oxathioamidate (<b>1</b>) was synthesised by the reaction between <i>O</i>-ethyl-thioxamate (oxalic acid-1-amide-2-<i>O</i>-ethyl ester) and ammonium hydrogen carbonate in water solution. Compound <b>1</b> was fully characterised by both microanalytical (elemental analysis, melting point determination) and spectroscopic means (FT-IR and NMR spectroscopy). Crystals suitable for single-crystal X-ray diffraction were isolated by slow evaporation of an ethanol solution of the compound. The analysis of the crystal packing reveals the prominent role exerted by intermolecular hydrogen bonding (HB) and chalcogen bonding (ChB) interactions.https://www.mdpi.com/1422-8599/2024/4/M1924thiooxamateoxalic acid derivativeshydrogen bondingXRD
spellingShingle M. Carla Aragoni
David B. Cordes
Anna Pintus
Enrico Podda
Riccardo Serra
Alexandra M. Z. Slawin
J. Derek Woollins
Massimiliano Arca
Ammonium Oxathioamidate
Molbank
thiooxamate
oxalic acid derivatives
hydrogen bonding
XRD
title Ammonium Oxathioamidate
title_full Ammonium Oxathioamidate
title_fullStr Ammonium Oxathioamidate
title_full_unstemmed Ammonium Oxathioamidate
title_short Ammonium Oxathioamidate
title_sort ammonium oxathioamidate
topic thiooxamate
oxalic acid derivatives
hydrogen bonding
XRD
url https://www.mdpi.com/1422-8599/2024/4/M1924
work_keys_str_mv AT mcarlaaragoni ammoniumoxathioamidate
AT davidbcordes ammoniumoxathioamidate
AT annapintus ammoniumoxathioamidate
AT enricopodda ammoniumoxathioamidate
AT riccardoserra ammoniumoxathioamidate
AT alexandramzslawin ammoniumoxathioamidate
AT jderekwoollins ammoniumoxathioamidate
AT massimilianoarca ammoniumoxathioamidate