CHNO Isomers: From Acetamide to 1,2-Oxazetidine and Beyond.

J Phys Chem A

School of Chemistry, National University of Ireland, Galway H91 TK33, Ireland.

Published: February 2022

AI Article Synopsis

  • * It discusses the relevance of these isomers to machine learning and AI applications, highlighting their significance in expanding the understanding of chemical bonding.
  • * The work also examines the contentious presence of acetamide in the ISM and proposes a feasible pathway for its formation via a specific chemical reaction involving ethanimidic acid and other abundant precursors.

Article Abstract

This work documents the properties of a number of isomers of molecular formula CHNO from the most stable, acetamide, through 1,2-oxazetidine and including even higher energy species largely of a dipolar nature. Only two of the isomers have been detected in emissions from the interstellar medium (ISM); possible further candidates are identified, and the likelihood of their being detectable is considered. In general, hardly any of these compounds have been discussed in the existing chemical literature, so this work represents an important contribution extending the canon of chemical bonding which can contribute to machine learning, providing a more exacting test of AI applications. The presence in the ISM of acetamide, CHC(O)NH, is the subject of current debate with no clear and obvious paths to its formation; it is shown that a 1,3-[H]-transfer from ()-ethanimidic acid, CHC(OH)═NH, is feasible in spite of an energy barrier of 130 kJ mol. It is speculated that imidic acid can itself be formed from abundant precursors, HO and CHC≡N, in an acid-induced, water addition, autocatalytic reaction on water-ice grains. HCC≡NHCC≡NH + HOHCC(OH)═NHHCC(OH)═NH + HO.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8859852PMC
http://dx.doi.org/10.1021/acs.jpca.1c09984DOI Listing

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