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Title: Interstellar formation of functionalized cyclopropenes
ABSTRACT

Nearly two decades since the detection of cyclopropenone (c-C3H2O) in the interstellar medium (ISM), the understanding of how this molecule comes to be remains incomplete. Many hypotheses place the ubiquitous hydrocarbon c-C3H2 at the centre of such discussions. However, insights into c-C3H2 chemistry are further complicated by the recent detection of ethynyl cyclopropenylidene (c-C3HC2H) and the observation of a radio line possibly belonging to methylenecyclopropene (c-C3H2CH2). In a necessary reconciliation of past and current work on the chemical capabilities of c-C3H2 in interstellar environments, the formation pathways of several functionalized cyclopropenes from c-C3H2 and a hydrogenated radical are explored. Chemically accurate CCSD(T)-F12/cc-pVTZ-F12 calculations are used to evaluate the energies of reaction and generate structures along the reaction pathway for formation products deemed chemically plausible. Potential energy scans are used to include or rule out certain paths to product formation based on conformation to the necessary requirements of cold interstellar chemistry. Four functionalized cyclopropenes in addition to c-C3H2O have net exothermic reactions when forming from c-C3H2 (c-C3H2CC, c-C3H2S, c-C3H2NH, and c-C3H2CH2). The former three are found to have reaction profiles favourable for formation in the cold ISM, while c-C3H2CH2 can only form by passage through an association barrier that must be mitigated by an energy source of some kind. c-C3H2S and c-C3H2NH are the best candidates for new spectroscopic searches. A complete detection of c-C3H2CH2 is necessary to fully understand cyclopropenylidene chemistry in the ISM.

 
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NSF-PAR ID:
10412596
Author(s) / Creator(s):
; ;
Publisher / Repository:
Oxford University Press
Date Published:
Journal Name:
Monthly Notices of the Royal Astronomical Society
Volume:
522
Issue:
3
ISSN:
0035-8711
Format(s):
Medium: X Size: p. 4215-4223
Size(s):
["p. 4215-4223"]
Sponsoring Org:
National Science Foundation
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