TY - JOUR
T1 - C2H5NO Isomers
T2 - From Acetamide to 1,2-Oxazetidine and Beyond
AU - Simmie, John M.
N1 - Publisher Copyright:
© 2022 The Author. Published by American Chemical Society
PY - 2022/2/17
Y1 - 2022/2/17
N2 - This work documents the properties of a number of isomers of molecular formula C2H5NO 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, CH3C(O)NH2, 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 (E,Z)-ethanimidic acid, CH3C(OH)═NH, is feasible in spite of an energy barrier of 130 kJ mol-1. It is speculated that imidic acid can itself be formed from abundant precursors, H2O and CH3C≡N, in an acid-induced, water addition, autocatalytic reaction on water-ice grains.
AB - This work documents the properties of a number of isomers of molecular formula C2H5NO 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, CH3C(O)NH2, 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 (E,Z)-ethanimidic acid, CH3C(OH)═NH, is feasible in spite of an energy barrier of 130 kJ mol-1. It is speculated that imidic acid can itself be formed from abundant precursors, H2O and CH3C≡N, in an acid-induced, water addition, autocatalytic reaction on water-ice grains.
UR - http://www.scopus.com/inward/record.url?scp=85124279012&partnerID=8YFLogxK
U2 - 10.1021/acs.jpca.1c09984
DO - 10.1021/acs.jpca.1c09984
M3 - Article
SN - 1089-5639
VL - 126
SP - 924
EP - 939
JO - Journal of Physical Chemistry A
JF - Journal of Physical Chemistry A
IS - 6
ER -