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Title: Direct D-atom Incorporation in Radicals: An Overlooked Pathway for Deuterium Fractionation
Abstract

Direct D-H exchange in radicals is investigated in a quasi-uniform flow employing chirped-pulse millimeter-wave spectroscopy. Inspired by the H-atom catalyzed isomerization of C3H2reported in our previous study, D-atom reactions with the propargyl (C3H3) radical and its photoproducts were investigated. We observed very efficient D-atom enrichment in the photoproducts through an analogous process of D addition/H elimination to C3H2isomers occurring at 40 K or below. Cyclic C3HD is the only deuterated isomer observed, consistent with the expected addition/elimination yielding the lowest energy product. The other expected addition/elimination product, deuterated propargyl, is not directly detected, although its presence is inferred by the observations in the latter part of the flow. There, in the high-density region of the flow, we observed both isotopomers of singly deuterated propyne attributed to stabilization of the H+C3H2D or D+C3H3adducts. The implications of these observations for the deuterium fractionation of hydrocarbon radicals in astrochemical environments is discussed with the support of a monodeuterated chemical kinetic model.

 
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Award ID(s):
1955239
NSF-PAR ID:
10397017
Author(s) / Creator(s):
; ; ; ;
Publisher / Repository:
DOI PREFIX: 10.3847
Date Published:
Journal Name:
The Astrophysical Journal
Volume:
944
Issue:
1
ISSN:
0004-637X
Format(s):
Medium: X Size: Article No. 77
Size(s):
["Article No. 77"]
Sponsoring Org:
National Science Foundation
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